Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Lungs of adult mice exposed to room air or hyperoxia as neonates were disassociated and stained for Ki-67 and VE-cadherin (CD144), PECAM (CD31) or CD45. ( A ) FACS plots show hyperoxia does not increase Ki-67 in CD144 + or CD31 + endothelial cells. n = 5 mice per plot. ( B ) FACS plots showing Ki-67 was not detected in CD45+ leukocytes. n = 5 mice per plot. ( C ) Lungs of adult Sftpc EGFP mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), EGFP (green), and counterstained with DAPI (blue). Arrow points to rare EGFP + AT2 cell expressing Ki-67. The proportion of EGFP + AT2 cells that also express Ki-67 were quantified and graphs as mean ± standard deviation. n = 10 mice per group. (Room air vs Hyperoxia: Not significant (NS)). ( D ) Lungs of adult Sftpc EGFP mice exposed to room air or hyperoxia were stained for phospho-histone H3 (Ser10) (red), EGFP (green), and counterstained with DAPI (blue). Arrow points to a phospho-histone H3 (Ser10) + cell that was rarely detected in mice exposed to room air or hyperoxia. Note that the phospho-histone H3 (Ser10) staining could not be done on the same tissues stained for Ki-67 because both antibodies were made in the same species. The proportion of pHH3+ to EGFP+ cells were quantified and graphed as mean ± standard deviation. n = 4 mice per group. (Room air vs Hyperoxia: NS= not significant). Scale bar in ( C , D ) = 50 μm. Data reflects biological replicates analyzed by Student’s t test ( C , D ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Expressing, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental model of exposing mice to hyperoxia and returning to room air. ( B ) Lungs of PND4 and adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates were immunostained for EGFP (green), SFTPC (red) or T1α (red), and counterstained with DAPI (blue). Hatched inset boxes are enlarged below individual images. The proportion of EGFP + and SFTPC + cells was quantified and graphed. n = 3 (RA PND4), 5 (O 2 PND4), 3 (RA PND56), and 3 (O 2 PND56). (Room Air vs Hyperoxia at PND56: P = 0.0005). The proportion of squamous EGFP + to cuboidal EGFP + staining was quantified and graphed. n = 10 (RA PND4), 10 (O 2 PND4), 8 (RA PND56), and 8 (O 2 PND56). (Room air vs Hyperoxia at PND56: P < 0.0001). ( C ) FACs analysis of EGFP + and HOPX + cells isolated from lungs of adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates. ( D ) FACS analysis of Ki-67+ cells that also express EGFP and HOPX. Data in ( B ) are graphed as mean ± standard deviation with individual samples shown as circles and squares. Scale bar in ( B ) = 50 μm and in ( C ) = 200 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( B ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Isolation, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental plan of exposing Mki67 CreERT ; Rosa26 mTmG to room air or hyperoxia as neonates, followed by tamoxifen as adults. ( B ) Lungs, trachea, and intestine from adult Mki67 CreERT ; Rosa26 mTmG administered tamoxifen were stained for EGFP (green), Ki-67 (red), and DAPI (blue). ( C ) Lungs of adult Mki 67 WT , Mki67 WT/CreERT , or Mki67 CreERT mice exposed to room air or hyperoxia as neonates were stained for Ki-67 (red) and DAPI (blue). The proportion of Ki-67 + cells were quantified and graphed. n = 10 mice per group. ( Mki67 WT : Room air vs Hyperoxia: P < 0.0001; Mki67 WT/CreERT : Room air vs Hyperoxia: P = 0.0010; Mki67 CreERT : Room air vs Hyperoxia: NS=not significant). ( D ) FACS plot of Ki-67 + cells detected in lungs of adult Mki67 WT exposed to room air or hyperoxia for comparison against Mki67 CreERT exposed to hyperoxia and FMO control after normalizing to NODE. ( E ) Expression of Ki-67 mRNA was determined in lungs of adult Mki67 WT and Mki67 CreERT mice exposed to room air or hyperoxia as neonates, normalized to 18S RNA, and graphed relative to Mki67 WT in room air. n = 4 mice per group. ( Mki67 WT Room air vs Mki67 WT Hyperoxia: P = 0.0034; Mki67 WT Hyperoxia vs Mki67 CreERT Room air: P < 0.0001; Mki67 WT Hyperoxia vs Mki67 CreERT Hyperoxia: P < 0.0001). Data in ( C , E ) are graphed as mean ± standard deviation with individual samples shown as triangles, circles, or squares. Scale bar in ( B ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( C , E ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Comparison, Control, Expressing, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) H&E stains of lungs from adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia. ( B ) Mean linear intercept of alveolar size in μm was measured in lungs of adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia and graphed as mean ± standard deviation. n = 10 mice per group. (RA- Mki76 WT vs O 2 Mki67 WT : P = 0.0005; RA Mki67 CreERT vs O 2 - Mki67 CreERT ; P < 0.0001). ( C ) Lungs from adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia were stained for SFTPC (red) and counterstained with DAPI (blue). ( D ) The proportion of SP-C + to DAPI + alveolar cells were quantified and graphed as mean ± standard deviation. n = 9 mice per group or 8 for Mki67 WT mice exposed to room air.(RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; RA Mki67 CreERT vs O 2 - Mki67 CreERT ; P = 0.0007). Data in ( B , D ) are graphed as mean ± SD with individual samples shown as circles or squares. Scale bar in ( A , C ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( B , D ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Standard Deviation, Staining

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia as neonates were infected with Hkx31 strain of IAV. ( A ) Neonatal hyperoxia significantly reduced the survival of infected Mki67 WT mice but not Mki67 CreERT mice. n = 10 per group. ( B ) Neonatal hyperoxia significantly increased weight loss of infected Mki67 WT mice but not Mki67 CreERT hypomorph mice. n = 10 mice per group. (Day 6: O 2 Mki67 CreERT vs RA Mki67 WT : P = 0.0202; Day 8: O 2 Mki67 CreERT vs RA Mki67 WT : P = 0.0.0196). ( C – F ) Lungs harvested on post-infection day 14 were stained with ( C ) Hematoxylin and Eosin to visualize pathology, ( D ) keratin 5 used to detect basal cells, ( E ) keratin 8 used to detect alveolar epithelial transitional cells, and ( F ) citrullinated histone H3 used to identify NETotic neutrophils. Arrows in ( D – F ) point respectively to keratin 5 + pods, keratin 8 + transitional cells, and citrullinated H3 + neutrophils. Data in ( B ) is graphed as mean weight loss after infection ± standard error of the mean. Scale bar in ( C , E ) = 50 μm and in ( D , F ) = 100 μm. Data reflects biological replicates analyzed by Log-Rank (Mantel–Cox) test in ( A ) and Student’s t test comparing individual post-infection days ( B ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT mice exposed to room air or hyperoxia were infected with Hkx31 IAV. ( A ) Lung sections collected on post-infection day 5 were stained with a TUNEL assay (green) used to detect DNA strand breaks and counterstained with DAPI (blue). ( B ) Adult Mki67 WT exposed to room air or hyperoxia were infected with Hkx31 IAV. Lung sections collected on post-infection day 5 were stained for TUNEL (red), antibody to T1α (green) used to detect AT1 cells, and counterstained with DAPI. Arrows point to patches of TUNEL+ cells with pseudo-yellow color in ( B ) reflecting TUNEL and T1α double-positive cells indicative of AT1 cell death. Images are representative of 10 mice per group with similar pathology. Scale bar in ( A ) = 100 μm, and ( B ) = 50 μm.

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining, TUNEL Assay

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Bronchoalveolar lavage washes were performed on adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia before and after infection with Hkx31 IAV. ( A ) The total number of leukocytes, ( B ) the proportion of macrophages, ( C ) the proportion of neutrophils, and ( D ) the proportion of lymphocytes were quantified and graphed n = 5 mice per group. ( A : D1: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0252; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0453; D3: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; d7: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0211; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0197). ( B : D1: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; D3: RA Mki67 WT vs O 2 Mki67 WT : P = 0.024; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0001; d5: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001). (C: D1: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; D3: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001, O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; d5: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0100; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0013; D7: O 2 Mki67 WT vs Mki67 CreERT : P = 0.0015). ( E ) Representative images of cytospins collected from mice on post-infection day 1. Arrows point to neutrophils in lavage collected from infected Mki67 WT mice exposed to hyperoxia Data in ( A – D ) is graphed as mean ± standard deviation with individual mice shown in circles or squares. Scale bar in ( E ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( A – D ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia as neonates were infected with Hkx31 IAV. ( A – F ) The expression of Cxcl1 , Cxlc2 , Cxcl4 , Cxcl5 , TNF-α, and IL-1β in lungs one day after infection was measured by qRT-PCR and graphed. n = 3 mice per group ( Cxcl1 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0341; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0341; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0399). ( Cxcl2 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0170; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0250; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0280). ( Cxcl5 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0045; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0055; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0052). (TNF-α: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0028; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0024; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0025). ( IL-1β : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0187; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0168; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0184). ( G ) Lungs of infected Mki67 WT mice exposed to room air or hyperoxia were immunostained for CXCL5 (red), T1α (green) and counterstained with DAPI (blue). Data in ( A – F ) is graphed as mean ± standard deviation with individual mice shown as circles or squares. Scale bar in ( G ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( A – F ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Expressing, Quantitative RT-PCR, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental plan for delivering pcDNA or pcDNA-Ki-67 expression plasmid using electroporation to lungs of adult Mki67 WT and Mki67 CreERT mice via electroporation. ( B ) Lungs were collected 48 h after gene delivery and immunostained for Ki-67 (red) and counterstained with DAPI (blue). ( C ) Bronchoalveolar lavages were performed 24 h after gene-delivered Mki67 WT and Mki67 CreERT mice were infected with Hkx31. The total number of leukocytes, the proportion of macrophages, the proportion of neutrophils, and the proportion of lymphocytes were quantified and graphed. n = 5 Mki67 WT with pcDNA or pcDNA-Ki-67, 7 Mki67 CreERT with pcDNA, and 6 Mki67 CreERT with pcDNA-Ki-67. (BAL Cells: Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P = 0.0005; Mki67 WT with pcDNA-Ki-67 vs Mki67 CreERT with pcDNA: P = 0.0288; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL macrophages: Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA: P < 0.0001; Mki67 WT with p cDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL neutrophils: Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL lymphocytes: NS = not significant). ( D ) Representative cytospin images. ( E ) qRT-PCR was used to assess expression of Cxcl1 , Cxlc2 , Cxcl4 , Cxcl5, TNF-α , and IL- 1β in lungs one day gene-delivered Mki67 WT and Mki67 CreERT mice were infected with Hkx31. mRNA expression was graphed as fold change relative to infected Mki67 WT mice transduced with control pcDNA plasmid. n = 4 mice per group. ( Cxcl1 , Cxcl2 , Cxcl5 , TNF-α , IL-1β : Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Cxcl5: NS = not significant). Data in ( C , E ) are graphed as mean ± standard deviation with individual mice shown as circles or squares. Scale bar in ( B ) = 100 μm and ( D ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( C , E ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Expressing, Plasmid Preparation, Electroporation, Infection, Quantitative RT-PCR, Transduction, Control, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon model showing the experimental plan for infecting Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT with a lethal dose of PR8 IAV. ( B ) Survival of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice infected with IAV. n = 8 mice per group. ( Mki67 CreERT vs Mki67 WT/CreERT vs Mki67 WT : P = 0.0283). ( C ) Weight loss in Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice infected with IAV. n = 8 mice per group. (Day 6: Mki67 CreERT vs Mki67 WT : P = 0.0047; Day 8: Mki67 CreERT vs Mki67 WT : P = 0.0106). ( D ) Inflammatory cell number and the percentage of macrophages and neutrophils were determined in BAL washes from Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 3. n = 5 mice per group. (BAL cells: Mki67 WT vs Mki67 WT/CreERT : P = 0.0209; Mki67 WT vs Mki67 CreERT : P = 0.0401; Mki67 WT/CreERT vs Mki67 CreERT : P = 0.0004). (BAL macrophages: Mki67 WT vs Mki67 WT/CreERT : P = 0.0012; Mki67 WT vs Mki67 CreERT : P = 0.0006). (BAL neutrophil: Mki67 WT vs Mki67 WT/CreERT : P = 0.0015; Mki67 WT vs Mki67 CreERT : P < 0.0001). ( E ) Representative cytospin images of BAL leukocytes collected from Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 3. ( F ) Lung pathology of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day on post-infection day 14. ( G ) Keratin 5 and keratin 8 staining in lungs of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 14. Data in ( C ) graphed a mean ± standard error of the mean and data in ( D ) graphed as mean ± standard deviation. Scale bar in ( E – G ) = 100 μm. Data reflect biological replicates analyzed by Log-Rank (Mantel–Cox) test in ( B ), Student’s t test comparing individual post-infection days ( C ), and one-way ANOVA using Tukey-Kramer HSD in ( D ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Bronchoalveolar lavages were performed 3 days after LPS (5 mg/kg) or PBS was instilled intratracheally into lungs of adult Mki67 WT and Mki67 CreERT hypomorph mice. ( B ) The total number of leukocytes, the proportion of macrophages, the proportion of neutrophils, and total protein were quantified in BAL fluid, and graphed as mean ± standard deviation with individual mice shown in circles or squares. n = 5 mice for all groups except 7 Mki67 CreERT exposed to LPS. (Total Cell Counts: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Percent macrophages: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Percent neutrophils: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Total Protein: PBS- Mki67 WT vs LPS- Mki67 WT : P = 0.0086; PBS- Mki67 CreERT vs LPS- Mki67 WT : P = 0.0006; LPS- Mki67 WT vs LPS- Mki67 CreERT : P = 0.0036). ( C ) Representative images of BAL cytospins obtained from the mice. Data in ( B ) graphed as mean ± standard deviation. Scale bar in ( C ) = 50 μm. Data reflects biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( B ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon model showing how mouse AT1.1 cells were created from EGFP + AT2 cells isolated from Immortomice. ( B ) Images showing loss of green fluorescence as EGFP+ AT2 cells from Immortomice were cultured. ( C ) PCR was used to detect Aqp5 , T1α , Sftpa , Sftpb , Sftpc , Nkx2.1 and β-actin in AT1.1, AT2.1, MLE15 and adult lungs. The amplified products were then visualized by gel electrophoresis. ( D ) QRT-PCR was used to detect AT1 and AT2-specific genes in AT1.1 cells, MLE15 cells, and postnatal day 7 (PND7) mouse lungs. Data for genes expressed by AT2 cells is graphed as fold change relative to MLE15 cells ± standard deviation. n = 3 per condition. ( Sftpa1 : MLE15 vs PND7: P = 0.0005; Sftpb : MLE15 vs PND7: P = 0.0005; Sftpc : MLE15 vs PND7: P < 0.0001; Sftpd : MLE15 vs PND7: P = 0.0011). Data for genes expressed by AT1 cells is graphed as fold change relative to AT1.1 cells ± standard deviation. ( T1α : AT1.1 vs PND7: P = 0.3259; Aqp5 : AT1.1 vs PND7: P = 0.0913; Hopx : AT1.1 vs MLE15: P = 0.0022; AT1.1 vs PND7: P = 0.1148; MLE15 vs PND7: P = 0.0245; Ifgbp2 : AT1.1 vs MLE15: P = 0.0004; AT1.1 vs PND7: P = 0.2554; MLE15 vs PND7: P = 0.0016; Gramd2 : At1.1 vs PND7: P = 0.1933). Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( D ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Isolation, Fluorescence, Cell Culture, Amplification, Nucleic Acid Electrophoresis, Quantitative RT-PCR, Standard Deviation

Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

Article Title: The Profile of Gut Microbiota in Carcinogenesis Driven by Mutant EGFR in Non–Small Cell Lung Cancer

doi: 10.4143/crt.2024.1177

Figure Lengend Snippet: Characterization of human lung-specific conditional EGFR L858R/T790M/C797S transgenic mice and preparation of stool from experimental mice. (A) Study design. EGFR L858R/T790M/C797S /CreER T2 mice were treated with tamoxifen (75 mg/kg) at 6 weeks. Human mutant EGFR expression and the occurrence of lung tumors were confirmed using an in vivo imaging system and magnetic resonance imaging at the indicated times. (B) Sample groups. F-mEGFR-sV1 (normal, V1); F-mEGFR-sV2 (mutant EGFR expression in lung tissue, V2); F-mEGFRsV3 (emergence of lung tumors, V3); V, stool collection.

Article Snippet: Lung-specific Sftpc-CreER T2 mice (strain #028054) were obtained from the Jackson Laboratory (Bar Harbor).

Techniques: Transgenic Assay, Mutagenesis, Expressing, In Vivo Imaging, Magnetic Resonance Imaging

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon of the experimental model. ( B ) Lungs of adult mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), T1α (green), and counterstained with DAPI (blue). Arrows point to Ki-67 + cells. The proportion of Ki-67 + cells to DAPI + nuclei were quantified and graphed. n = 10 mice per group. (Room air vs Hyperoxia: P < 0.0001). ( C ) Flow cytometric plots of Ki-67 + cells detected in disassociated lungs of adult mice exposed to room air or hyperoxia compared to FMO control. The proportion of Ki-67 + cells in 10,000 cells was quantified and graphed. n = 3 mice per group. (Room air vs Hyperoxia: P = 0.00135). ( D ) Flow cytometric plots of Ki-67 + and HOPX + cells detected in lungs of adult mice exposed to room air or hyperoxia as neonates. The percentage of double-positive cells in 10,000 cells is shown in the embedded box. ( E ) Lungs of adult Aqp5 Cre ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates were immunostained for EGFP (green) and T1α (red) or EGFP (green) and Ki-67 (red) with DAPI (blue) counterstaining. FACS plots of Ki-67 + and EGFP + cells from Aqp5 Cre ; Rosa26 mTmG exposed to room air or hyperoxia as neonates. ( F ) Lungs of adult mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), BrdU (green), and counterstained with DAPI. Arrows point to BrdU + cells. The proportion of BrdU+ cells to DAPI+ nuclei was graphed. n = 9 mice per group. NS not significant. Data in ( B, C , F ) are graphed as mean ± standard deviation with individual values shown as circles or squares. Scale bar in ( B ) = 30 μm and ( E , F ) = 50 μm. Data reflect biological replicates analyzed by Student’s t test in ( B , C , F ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Control, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Lungs of adult mice exposed to room air or hyperoxia as neonates were disassociated and stained for Ki-67 and VE-cadherin (CD144), PECAM (CD31) or CD45. ( A ) FACS plots show hyperoxia does not increase Ki-67 in CD144 + or CD31 + endothelial cells. n = 5 mice per plot. ( B ) FACS plots showing Ki-67 was not detected in CD45+ leukocytes. n = 5 mice per plot. ( C ) Lungs of adult Sftpc EGFP mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), EGFP (green), and counterstained with DAPI (blue). Arrow points to rare EGFP + AT2 cell expressing Ki-67. The proportion of EGFP + AT2 cells that also express Ki-67 were quantified and graphs as mean ± standard deviation. n = 10 mice per group. (Room air vs Hyperoxia: Not significant (NS)). ( D ) Lungs of adult Sftpc EGFP mice exposed to room air or hyperoxia were stained for phospho-histone H3 (Ser10) (red), EGFP (green), and counterstained with DAPI (blue). Arrow points to a phospho-histone H3 (Ser10) + cell that was rarely detected in mice exposed to room air or hyperoxia. Note that the phospho-histone H3 (Ser10) staining could not be done on the same tissues stained for Ki-67 because both antibodies were made in the same species. The proportion of pHH3+ to EGFP+ cells were quantified and graphed as mean ± standard deviation. n = 4 mice per group. (Room air vs Hyperoxia: NS= not significant). Scale bar in ( C , D ) = 50 μm. Data reflects biological replicates analyzed by Student’s t test ( C , D ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Expressing, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental model of exposing mice to hyperoxia and returning to room air. ( B ) Lungs of PND4 and adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates were immunostained for EGFP (green), SFTPC (red) or T1α (red), and counterstained with DAPI (blue). Hatched inset boxes are enlarged below individual images. The proportion of EGFP + and SFTPC + cells was quantified and graphed. n = 3 (RA PND4), 5 (O 2 PND4), 3 (RA PND56), and 3 (O 2 PND56). (Room Air vs Hyperoxia at PND56: P = 0.0005). The proportion of squamous EGFP + to cuboidal EGFP + staining was quantified and graphed. n = 10 (RA PND4), 10 (O 2 PND4), 8 (RA PND56), and 8 (O 2 PND56). (Room air vs Hyperoxia at PND56: P < 0.0001). ( C ) FACs analysis of EGFP + and HOPX + cells isolated from lungs of adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates. ( D ) FACS analysis of Ki-67+ cells that also express EGFP and HOPX. Data in ( B ) are graphed as mean ± standard deviation with individual samples shown as circles and squares. Scale bar in ( B ) = 50 μm and in ( C ) = 200 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( B ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Isolation, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental plan of exposing Mki67 CreERT ; Rosa26 mTmG to room air or hyperoxia as neonates, followed by tamoxifen as adults. ( B ) Lungs, trachea, and intestine from adult Mki67 CreERT ; Rosa26 mTmG administered tamoxifen were stained for EGFP (green), Ki-67 (red), and DAPI (blue). ( C ) Lungs of adult Mki 67 WT , Mki67 WT/CreERT , or Mki67 CreERT mice exposed to room air or hyperoxia as neonates were stained for Ki-67 (red) and DAPI (blue). The proportion of Ki-67 + cells were quantified and graphed. n = 10 mice per group. ( Mki67 WT : Room air vs Hyperoxia: P < 0.0001; Mki67 WT/CreERT : Room air vs Hyperoxia: P = 0.0010; Mki67 CreERT : Room air vs Hyperoxia: NS=not significant). ( D ) FACS plot of Ki-67 + cells detected in lungs of adult Mki67 WT exposed to room air or hyperoxia for comparison against Mki67 CreERT exposed to hyperoxia and FMO control after normalizing to NODE. ( E ) Expression of Ki-67 mRNA was determined in lungs of adult Mki67 WT and Mki67 CreERT mice exposed to room air or hyperoxia as neonates, normalized to 18S RNA, and graphed relative to Mki67 WT in room air. n = 4 mice per group. ( Mki67 WT Room air vs Mki67 WT Hyperoxia: P = 0.0034; Mki67 WT Hyperoxia vs Mki67 CreERT Room air: P < 0.0001; Mki67 WT Hyperoxia vs Mki67 CreERT Hyperoxia: P < 0.0001). Data in ( C , E ) are graphed as mean ± standard deviation with individual samples shown as triangles, circles, or squares. Scale bar in ( B ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( C , E ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Comparison, Control, Expressing, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) H&E stains of lungs from adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia. ( B ) Mean linear intercept of alveolar size in μm was measured in lungs of adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia and graphed as mean ± standard deviation. n = 10 mice per group. (RA- Mki76 WT vs O 2 Mki67 WT : P = 0.0005; RA Mki67 CreERT vs O 2 - Mki67 CreERT ; P < 0.0001). ( C ) Lungs from adult Mki67 WT and Mki67 CreERT hypomorph mice exposed to room air or hyperoxia were stained for SFTPC (red) and counterstained with DAPI (blue). ( D ) The proportion of SP-C + to DAPI + alveolar cells were quantified and graphed as mean ± standard deviation. n = 9 mice per group or 8 for Mki67 WT mice exposed to room air.(RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; RA Mki67 CreERT vs O 2 - Mki67 CreERT ; P = 0.0007). Data in ( B , D ) are graphed as mean ± SD with individual samples shown as circles or squares. Scale bar in ( A , C ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( B , D ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Standard Deviation, Staining

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia as neonates were infected with Hkx31 strain of IAV. ( A ) Neonatal hyperoxia significantly reduced the survival of infected Mki67 WT mice but not Mki67 CreERT mice. n = 10 per group. ( B ) Neonatal hyperoxia significantly increased weight loss of infected Mki67 WT mice but not Mki67 CreERT hypomorph mice. n = 10 mice per group. (Day 6: O 2 Mki67 CreERT vs RA Mki67 WT : P = 0.0202; Day 8: O 2 Mki67 CreERT vs RA Mki67 WT : P = 0.0.0196). ( C – F ) Lungs harvested on post-infection day 14 were stained with ( C ) Hematoxylin and Eosin to visualize pathology, ( D ) keratin 5 used to detect basal cells, ( E ) keratin 8 used to detect alveolar epithelial transitional cells, and ( F ) citrullinated histone H3 used to identify NETotic neutrophils. Arrows in ( D – F ) point respectively to keratin 5 + pods, keratin 8 + transitional cells, and citrullinated H3 + neutrophils. Data in ( B ) is graphed as mean weight loss after infection ± standard error of the mean. Scale bar in ( C , E ) = 50 μm and in ( D , F ) = 100 μm. Data reflects biological replicates analyzed by Log-Rank (Mantel–Cox) test in ( A ) and Student’s t test comparing individual post-infection days ( B ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT mice exposed to room air or hyperoxia were infected with Hkx31 IAV. ( A ) Lung sections collected on post-infection day 5 were stained with a TUNEL assay (green) used to detect DNA strand breaks and counterstained with DAPI (blue). ( B ) Adult Mki67 WT exposed to room air or hyperoxia were infected with Hkx31 IAV. Lung sections collected on post-infection day 5 were stained for TUNEL (red), antibody to T1α (green) used to detect AT1 cells, and counterstained with DAPI. Arrows point to patches of TUNEL+ cells with pseudo-yellow color in ( B ) reflecting TUNEL and T1α double-positive cells indicative of AT1 cell death. Images are representative of 10 mice per group with similar pathology. Scale bar in ( A ) = 100 μm, and ( B ) = 50 μm.

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining, TUNEL Assay

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Bronchoalveolar lavage washes were performed on adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia before and after infection with Hkx31 IAV. ( A ) The total number of leukocytes, ( B ) the proportion of macrophages, ( C ) the proportion of neutrophils, and ( D ) the proportion of lymphocytes were quantified and graphed n = 5 mice per group. ( A : D1: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0252; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0453; D3: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; d7: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0211; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0197). ( B : D1: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; D3: RA Mki67 WT vs O 2 Mki67 WT : P = 0.024; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0001; d5: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001). (C: D1: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001; O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; D3: RA Mki67 WT vs O 2 Mki67 WT : P < 0.0001, O 2 Mki67 WT vs Mki67 CreERT : P < 0.0001; d5: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0100; O 2 Mki67 WT vs Mki67 CreERT : P = 0.0013; D7: O 2 Mki67 WT vs Mki67 CreERT : P = 0.0015). ( E ) Representative images of cytospins collected from mice on post-infection day 1. Arrows point to neutrophils in lavage collected from infected Mki67 WT mice exposed to hyperoxia Data in ( A – D ) is graphed as mean ± standard deviation with individual mice shown in circles or squares. Scale bar in ( E ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( A – D ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: Adult Mki67 WT and Mki67 CreERT exposed to room air or hyperoxia as neonates were infected with Hkx31 IAV. ( A – F ) The expression of Cxcl1 , Cxlc2 , Cxcl4 , Cxcl5 , TNF-α, and IL-1β in lungs one day after infection was measured by qRT-PCR and graphed. n = 3 mice per group ( Cxcl1 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0341; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0341; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0399). ( Cxcl2 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0170; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0250; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0280). ( Cxcl5 : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0045; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0055; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0052). (TNF-α: RA Mki67 WT vs O 2 Mki67 WT : P = 0.0028; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0024; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0025). ( IL-1β : RA Mki67 WT vs O 2 Mki67 WT : P = 0.0187; O 2 Mki67 WT vs RA Mki67 CreERT : P = 0.0168; O 2 Mki67 WT vs O 2 Mki67 CreERT : P = 0.0184). ( G ) Lungs of infected Mki67 WT mice exposed to room air or hyperoxia were immunostained for CXCL5 (red), T1α (green) and counterstained with DAPI (blue). Data in ( A – F ) is graphed as mean ± standard deviation with individual mice shown as circles or squares. Scale bar in ( G ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( A – F ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Expressing, Quantitative RT-PCR, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental plan for delivering pcDNA or pcDNA-Ki-67 expression plasmid using electroporation to lungs of adult Mki67 WT and Mki67 CreERT mice via electroporation. ( B ) Lungs were collected 48 h after gene delivery and immunostained for Ki-67 (red) and counterstained with DAPI (blue). ( C ) Bronchoalveolar lavages were performed 24 h after gene-delivered Mki67 WT and Mki67 CreERT mice were infected with Hkx31. The total number of leukocytes, the proportion of macrophages, the proportion of neutrophils, and the proportion of lymphocytes were quantified and graphed. n = 5 Mki67 WT with pcDNA or pcDNA-Ki-67, 7 Mki67 CreERT with pcDNA, and 6 Mki67 CreERT with pcDNA-Ki-67. (BAL Cells: Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P = 0.0005; Mki67 WT with pcDNA-Ki-67 vs Mki67 CreERT with pcDNA: P = 0.0288; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL macrophages: Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA: P < 0.0001; Mki67 WT with p cDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL neutrophils: Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA: P < 0.0001; Mki67 WT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001). (BAL lymphocytes: NS = not significant). ( D ) Representative cytospin images. ( E ) qRT-PCR was used to assess expression of Cxcl1 , Cxlc2 , Cxcl4 , Cxcl5, TNF-α , and IL- 1β in lungs one day gene-delivered Mki67 WT and Mki67 CreERT mice were infected with Hkx31. mRNA expression was graphed as fold change relative to infected Mki67 WT mice transduced with control pcDNA plasmid. n = 4 mice per group. ( Cxcl1 , Cxcl2 , Cxcl5 , TNF-α , IL-1β : Mki67 WT with pcDNA vs Mki67 WT with pcDNA-Ki-67: P < 0.0001; Mki67 CreERT with pcDNA vs Mki67 CreERT with pcDNA-Ki-67: P < 0.0001; Cxcl5: NS = not significant). Data in ( C , E ) are graphed as mean ± standard deviation with individual mice shown as circles or squares. Scale bar in ( B ) = 100 μm and ( D ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( C , E ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Expressing, Plasmid Preparation, Electroporation, Infection, Quantitative RT-PCR, Transduction, Control, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon model showing the experimental plan for infecting Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT with a lethal dose of PR8 IAV. ( B ) Survival of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice infected with IAV. n = 8 mice per group. ( Mki67 CreERT vs Mki67 WT/CreERT vs Mki67 WT : P = 0.0283). ( C ) Weight loss in Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice infected with IAV. n = 8 mice per group. (Day 6: Mki67 CreERT vs Mki67 WT : P = 0.0047; Day 8: Mki67 CreERT vs Mki67 WT : P = 0.0106). ( D ) Inflammatory cell number and the percentage of macrophages and neutrophils were determined in BAL washes from Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 3. n = 5 mice per group. (BAL cells: Mki67 WT vs Mki67 WT/CreERT : P = 0.0209; Mki67 WT vs Mki67 CreERT : P = 0.0401; Mki67 WT/CreERT vs Mki67 CreERT : P = 0.0004). (BAL macrophages: Mki67 WT vs Mki67 WT/CreERT : P = 0.0012; Mki67 WT vs Mki67 CreERT : P = 0.0006). (BAL neutrophil: Mki67 WT vs Mki67 WT/CreERT : P = 0.0015; Mki67 WT vs Mki67 CreERT : P < 0.0001). ( E ) Representative cytospin images of BAL leukocytes collected from Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 3. ( F ) Lung pathology of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day on post-infection day 14. ( G ) Keratin 5 and keratin 8 staining in lungs of Mki67 WT , Mki67 WT/CreERT , and Mki67 CreERT mice on post-infection day 14. Data in ( C ) graphed a mean ± standard error of the mean and data in ( D ) graphed as mean ± standard deviation. Scale bar in ( E – G ) = 100 μm. Data reflect biological replicates analyzed by Log-Rank (Mantel–Cox) test in ( B ), Student’s t test comparing individual post-infection days ( C ), and one-way ANOVA using Tukey-Kramer HSD in ( D ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Infection, Staining, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Bronchoalveolar lavages were performed 3 days after LPS (5 mg/kg) or PBS was instilled intratracheally into lungs of adult Mki67 WT and Mki67 CreERT hypomorph mice. ( B ) The total number of leukocytes, the proportion of macrophages, the proportion of neutrophils, and total protein were quantified in BAL fluid, and graphed as mean ± standard deviation with individual mice shown in circles or squares. n = 5 mice for all groups except 7 Mki67 CreERT exposed to LPS. (Total Cell Counts: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Percent macrophages: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Percent neutrophils: PBS- Mki67 WT vs LPS- Mki67 WT : P < 0.0001; PBS- Mki67 CreERT vs LPS- Mki67 WT : P < 0.0001; LPS- Mki67 WT vs LPS- Mki67 CreERT : P < 0.0001). (Total Protein: PBS- Mki67 WT vs LPS- Mki67 WT : P = 0.0086; PBS- Mki67 CreERT vs LPS- Mki67 WT : P = 0.0006; LPS- Mki67 WT vs LPS- Mki67 CreERT : P = 0.0036). ( C ) Representative images of BAL cytospins obtained from the mice. Data in ( B ) graphed as mean ± standard deviation. Scale bar in ( C ) = 50 μm. Data reflects biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( B ).

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) AT1.1 cells transfected with Ki-67 siRNA for 48 h were fixed and stained for Ki-67 (magenta) and counterstained with DAPI (blue). Scale bar = 50 μm. ( B ) AT1.1 cells were transfected with Ki-67 siRNA or control oligonucleotides. The equal number of cells were plated on day 0 and counted 24 and 48 h later. Data is graphed as a mean number of cells ± standard deviation. n = 3 cultures per group. ( C ) AT1.1 cells were transfected with Ki-67 or a scrambled control for 48 h. The cells were then transfected with NF-κB-luciferase reporter and cultured for an additional 24 h in control media or media containing 0.5 ng/ml IL-1β. Luciferase activity was then graphed as mean fold change ± standard deviation relative to control cells cultured in the absence of IL-1β. n = 6 cultures per group. (IL-1β vs control: P = 0.0003; IL-1β vs IL-1β and siKi67: P < 0.0001). ( D ) AT1.1 cells were transfected with Ki-67 siRNA or scrambled controls for 48 h and then cultured for 24 h in 0.5 ng/ml IL-1β or control media. QRT-PCR was used to detect expression of Ki-67 , RelA , Cxcl1 , Cxcl5 , and IL-6 . Data are graphed as mean fold change ± standard deviation compared to control cells. n = 6 for assessing siKi67 on Ki-67 , RelA , Cxcl1 , and Cxlc5 expression and n = 4 for all other measurements. ( Ki-67 , RelA , Cxcl1 , Cxcl5 , and IL-6 : Control vs siKi67 cells: P < 0.0001; SiKi67 vs IL-1β cells: P < 0.0001; IL-1β vs IL-1β and siKi67 cells: P < 0.0001). ( RelA : Control vs siRelA cells: P < 0.002; Control vs IL-1β cells: P = 0.0003; siRelA vs Il-1β cells: P < 0.0001; Il-1β vs siRelA and IL-1β: P < 0.0001). ( Cxcl1 : Control vs siRelA cells: P < 0.0052; Control vs IL-1β cells: P = 0.0127; siRelA vs Il-1β cells: P < 0.0001; Il-1β vs siRelA and IL-1β: P < 0.0001). ( Cxcl5 : Control vs IL-1β cells: P = 0.0072; siRelA vs Il-1β cells: P = 0.0020; Il-1β vs siRelA and IL-1β: P = 0.0051). (IL-6: Control vs siRelA cells: P = 0.0290; Control vs IL-1β cells: P < 0.0001; siRelA vs Il-1β cells: P < 0.0001; Il-1β vs siRelA and IL-1β: P < 0.0001). Data in ( B – D ) graphed as mean ± standard deviation. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD ( B – D ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Transfection, Staining, Control, Standard Deviation, Luciferase, Cell Culture, Activity Assay, Quantitative RT-PCR, Expressing

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon of the experimental model. ( B ) Lungs of adult mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), T1α (green), and counterstained with DAPI (blue). Arrows point to Ki-67 + cells. The proportion of Ki-67 + cells to DAPI + nuclei were quantified and graphed. n = 10 mice per group. (Room air vs Hyperoxia: P < 0.0001). ( C ) Flow cytometric plots of Ki-67 + cells detected in disassociated lungs of adult mice exposed to room air or hyperoxia compared to FMO control. The proportion of Ki-67 + cells in 10,000 cells was quantified and graphed. n = 3 mice per group. (Room air vs Hyperoxia: P = 0.00135). ( D ) Flow cytometric plots of Ki-67 + and HOPX + cells detected in lungs of adult mice exposed to room air or hyperoxia as neonates. The percentage of double-positive cells in 10,000 cells is shown in the embedded box. ( E ) Lungs of adult Aqp5 Cre ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates were immunostained for EGFP (green) and T1α (red) or EGFP (green) and Ki-67 (red) with DAPI (blue) counterstaining. FACS plots of Ki-67 + and EGFP + cells from Aqp5 Cre ; Rosa26 mTmG exposed to room air or hyperoxia as neonates. ( F ) Lungs of adult mice exposed to room air or hyperoxia as neonates were immunostained for Ki-67 (red), BrdU (green), and counterstained with DAPI. Arrows point to BrdU + cells. The proportion of BrdU+ cells to DAPI+ nuclei was graphed. n = 9 mice per group. NS not significant. Data in ( B, C , F ) are graphed as mean ± standard deviation with individual values shown as circles or squares. Scale bar in ( B ) = 30 μm and ( E , F ) = 50 μm. Data reflect biological replicates analyzed by Student’s t test in ( B , C , F ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Control, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental model of exposing mice to hyperoxia and returning to room air. ( B ) Lungs of PND4 and adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates were immunostained for EGFP (green), SFTPC (red) or T1α (red), and counterstained with DAPI (blue). Hatched inset boxes are enlarged below individual images. The proportion of EGFP + and SFTPC + cells was quantified and graphed. n = 3 (RA PND4), 5 (O 2 PND4), 3 (RA PND56), and 3 (O 2 PND56). (Room Air vs Hyperoxia at PND56: P = 0.0005). The proportion of squamous EGFP + to cuboidal EGFP + staining was quantified and graphed. n = 10 (RA PND4), 10 (O 2 PND4), 8 (RA PND56), and 8 (O 2 PND56). (Room air vs Hyperoxia at PND56: P < 0.0001). ( C ) FACs analysis of EGFP + and HOPX + cells isolated from lungs of adult Sftpc CreERT ; Rosa26 mTmG mice exposed to room air or hyperoxia as neonates. ( D ) FACS analysis of Ki-67+ cells that also express EGFP and HOPX. Data in ( B ) are graphed as mean ± standard deviation with individual samples shown as circles and squares. Scale bar in ( B ) = 50 μm and in ( C ) = 200 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( B ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Isolation, Standard Deviation

Journal: EMBO Molecular Medicine

Article Title: Ki-67 promotes inflammatory signaling governing neutrophil recruitment during respiratory infections

doi: 10.1038/s44321-025-00261-z

Figure Lengend Snippet: ( A ) Cartoon showing the experimental plan of exposing Mki67 CreERT ; Rosa26 mTmG to room air or hyperoxia as neonates, followed by tamoxifen as adults. ( B ) Lungs, trachea, and intestine from adult Mki67 CreERT ; Rosa26 mTmG administered tamoxifen were stained for EGFP (green), Ki-67 (red), and DAPI (blue). ( C ) Lungs of adult Mki 67 WT , Mki67 WT/CreERT , or Mki67 CreERT mice exposed to room air or hyperoxia as neonates were stained for Ki-67 (red) and DAPI (blue). The proportion of Ki-67 + cells were quantified and graphed. n = 10 mice per group. ( Mki67 WT : Room air vs Hyperoxia: P < 0.0001; Mki67 WT/CreERT : Room air vs Hyperoxia: P = 0.0010; Mki67 CreERT : Room air vs Hyperoxia: NS=not significant). ( D ) FACS plot of Ki-67 + cells detected in lungs of adult Mki67 WT exposed to room air or hyperoxia for comparison against Mki67 CreERT exposed to hyperoxia and FMO control after normalizing to NODE. ( E ) Expression of Ki-67 mRNA was determined in lungs of adult Mki67 WT and Mki67 CreERT mice exposed to room air or hyperoxia as neonates, normalized to 18S RNA, and graphed relative to Mki67 WT in room air. n = 4 mice per group. ( Mki67 WT Room air vs Mki67 WT Hyperoxia: P = 0.0034; Mki67 WT Hyperoxia vs Mki67 CreERT Room air: P < 0.0001; Mki67 WT Hyperoxia vs Mki67 CreERT Hyperoxia: P < 0.0001). Data in ( C , E ) are graphed as mean ± standard deviation with individual samples shown as triangles, circles, or squares. Scale bar in ( B ) = 50 μm. Data reflect biological replicates analyzed by one-way ANOVA using Tukey-Kramer HSD in ( C , E ). .

Article Snippet: C57BL/6J (RRID:IMSR_JAX:000664), Mki67 CreERT (RRID:IMSR_JAX:0229803), R26 mTmG (RRID:IMSR_JAX:007676), and Sftpc CreERT (RRID:IMSR_JAX:028054) mice were purchased from the Jackson Laboratories (Bar Harbor, ME).

Techniques: Staining, Comparison, Control, Expressing, Standard Deviation