Journal: Nature Communications

Article Title: Distinct fibroblast subsets regulate lacteal integrity through YAP/TAZ-induced VEGF-C in intestinal villi

doi: 10.1038/s41467-020-17886-y

Figure Lengend Snippet: a Diagram depicting the generation of tdTomato rPβC mouse and PDGFRβ + cell-specific expression of tdTomato from 8-week old and their analyses at 10-week old. b Illustration of droplet-based single-cell RNA sequencing (scRNA-seq) of PDGFRβ + tdTomato + IntSCs sorted from the small intestine of tdTomato rPβC mice. c Visualization of unsupervised clustering of 7 distinct PDGFRβ + IntSC clusters by Uniform manifold approximation and projection (UMAP) in the small intestine of tdTomato rPβC mice. vFB, intestinal villi fibroblast; FB, fibroblast; SMC, smooth muscle cell; MC, mural cell. d Heatmap displaying the scaled expression patterns of top ten differentially expressed genes for random sampled cells (maximum thousand cells) for each indicated clusters. e List of representative marker genes of each of the seven PDGFRβ + IntSC clusters (left) and violin plots (right) showing the expression of top-ranking marker genes for each cluster. Log normalized read counts as y -axis (normalized expression). f UMAP visualization of unsupervised clustering of seven distinct PDGFRβ + IntSC clusters in the small intestine of Lats1/2 iΔ - tdTomato rPβC mice. g Gene expression levels of Vegfc and Vegfa in tdTomato rPβC and Lats1/2 iΔ - tdTomato rPβC mice projected on UMAP plot. Note that specific subsets of PDGFRβ + IntSCs (vFB1-3) in the small intestine of Lats1/2 iΔ - tdTomato rPβC mice show higher expression of Vegfc compared with those of tdTomato rPβC mice. h , i Representative images of PDGFRβ + IntSCs in WT mouse reveal expressions of each fibroblast-specific markers: PAI-1 + vFB1, Serpina3n + vFB2, P2X1 + vFB3, Ackr4 + or Grem1 + FB4, and PDGFRα + Sox6 + FB5. Each white box in the lower left corner is a magnified view. White asterisks indicate lacteals and white arrowheads indicate each fibroblast cluster-specific cell type stained with the indicated marker. Similar findings were observed in n = 4 mice from two independent experiments. Scale bars, 20 μm. j Schematic images depicting the anatomic distribution of indicated markers for vFB1-3, FB4, FB5, SMC, MC, capillary plexus, and lacteal in intestinal villi of adult WT mouse. vFB1-3 are uniformly distributed around the lacteal, whereas FB4 is mainly located in the submucosal area and FB5 is mostly placed under the intestinal epithelium. Black dashed boxes are magnified in the right panels.

Article Snippet: The following primary and secondary antibodies were used in the immunostaining with smFISH: anti-PDGFRβ (rat monoclonal, ab91066, Abcam); anti-Shisa3 (rabbit polyclonal, TA320118, Origene); anti-P2X1 (rabbit polyclonal, APR-001, Alomone labs) and Alexa Fluor 488-, Alexa Fluor 594-, Alexa Fluor 647-conjugated secondary antibodies were purchased from Jackson ImmunoResearch.

Techniques: Expressing, RNA Sequencing Assay, Marker, Staining

Journal: Nature Communications

Article Title: Distinct fibroblast subsets regulate lacteal integrity through YAP/TAZ-induced VEGF-C in intestinal villi

doi: 10.1038/s41467-020-17886-y

Figure Lengend Snippet: a Representative images of vFB3 (P2X1 + Serpina3n + PDGFRβ + ) and vFB1-2 (P2X1 - Serpina3n + PDGFRβ + ) in WT mouse. Similar findings were observed in n = 4 mice from two independent experiments. White and yellow dotted boxes are magnified in the upper right and lower right panels, respectively. Red and yellow arrowheads indicate vFB3 and vFB1-2, respectively. Scale bar, 20 μm. b Representative images of vFB1 (Serpina3n + Fosb + Shisa3 + PDGFRβ + ) and vFB2 (Serpina3n + Fosb - Shisa3 + PDGFRβ + ) in WT mouse. Similar findings were observed in n = 4 mice from two independent experiments. White and yellow dotted boxes are magnified in the upper right and lower right panels, respectively, for each image. White and yellow arrowheads indicate vFB1 and vFB2, respectively. Scale bars, 20 μm. c Representative images of Vegfc single-molecule fluorescence in situ hybridization (smFISH) in intestinal villi of tdTomato rPβC and Lats1/2 iΔ - tdTomato rPβC mice. Similar findings were observed in n = 4 mice/group from two independent experiments. White dotted boxes are magnified in the right panel. Scale bars, 20 μm. d Representative images of Vegfc smFISH in vFB1-3 of WT and Lats1/2 iΔ - tdTomato rPβC mice. Similar findings were observed in n = 4 mice/group from two independent experiments. White and yellow dotted boxes are magnified in the upper right and lower right panels, respectively, for each image. Scale bars, 20 μm.

Article Snippet: The following primary and secondary antibodies were used in the immunostaining with smFISH: anti-PDGFRβ (rat monoclonal, ab91066, Abcam); anti-Shisa3 (rabbit polyclonal, TA320118, Origene); anti-P2X1 (rabbit polyclonal, APR-001, Alomone labs) and Alexa Fluor 488-, Alexa Fluor 594-, Alexa Fluor 647-conjugated secondary antibodies were purchased from Jackson ImmunoResearch.

Techniques: Fluorescence, In Situ Hybridization

Journal: Scientific Reports

Article Title: Dysfunction of low-density neutrophils in peripheral circulation in patients with sepsis

doi: 10.1038/s41598-021-04682-x

Figure Lengend Snippet: Reduced chemotactic function of LDNs. ( A ) Neutrophil chemotaxis toward fMLP was assayed. CD (chemotactic distance, μm), CCR (chemo cell ratio, cell number of zone I + II + III/Total cells in the side well, %), CI (chemo index, cell number of zone II + III/ Total number of chemotactic cells, %). ( B – D ) The evaluation indicators CD, CCR, and CI were significantly reduced in neutrophil chemotactic function evaluations of LDN. ( E ) The expression of P2X1 on HDNs and LDNs was analyzed using flow cytometry.

Article Snippet: Antibodies used in the experiment include CD66b (G10F5, BD Pharmingen, USA), CD10 (HI10α, Biolegend, USA) CXCR4 (12G5, Biolegend, USA) and P2X1 (APR-022-F, Alomone labs, Israel).

Techniques: Chemotaxis Assay, Expressing, Flow Cytometry

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a Volcano plots of differential gene expression in 145 primary PDAC, 46 adjacent pancreases, 25 liver metastases and 27 adjacent livers. Red dots represent upregulated immune-related genes, and blue dots represent downregulated immune-related genes. b Immunome analyses of 26 infiltrating immune cell types in adjacent pancreas, primary PDAC, adjacent liver tissue and metastatic PDAC samples. c GO Biological Process analyses of differentially expressed genes between adjacent liver tissue and metastatic PDAC samples. d Expression analyses of P2RX1 in the adjacent pancreas, primary PDAC, adjacent liver tissue and metastatic PDAC samples from the GSE71729 and Renji cohorts. e Correlation analyses between P2RX1 and immune checkpoint molecules in metastatic PDAC samples. Bars represent mean ± standard deviation in ( d ). * P < 0.05, ** P < 0.01, and *** P < 0.001, by one-way ANOVA and Tukey’s multiple comparisons test ( d left), or Student’s t test ( d right). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Expressing, Standard Deviation

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a , b P2rx1 −/− mice were generated using CRISPR/Cas9 system. Schematic diagram was shown in ( a ) and genotyping results were shown in ( b ) (representative result from three independent experiments). c , d KPC cells were intrasplenically injected to seed livers of WT and P2rx1 −/− mice, and in vivo imaging was performed at sequential times. Representative images are shown in ( c ), and quantitative results are shown in ( d ) ( n = 6 per group, three independent experiments). e Representative images of liver metastatic samples harvested at day 17. f Liver weight of liver metastatic samples was measured at day 17 ( n = 5 per group, two independent experiments). g Survival analysis of liver metastatic WT or P2rx1 −/− mice within a duration of 5 weeks ( n = 10 per group, two independent experiments). h Normal liver (D0) and two sequential stages (D3 and D17) of liver metastases in WT and P2rx1 −/− mice were harvested for RNA-seq, and PCA analyses were performed ( n = 3 for D0, n = 4 for D3 and D17). i Representative Ki67 immunohistochemical staining of WT and P2rx1 −/− liver metastases at day 17 ( n = 4 per group, two independent experiments). 100 μm of scale bar for low power fields, 25 μm of scale bar for high power fields. j Heatmap of immune checkpoint molecules in liver metastases of WT or P2rx1 −/− mice at D3 and D17 ( n = 4 per group). Bars represent mean ± standard deviation in ( d , f ). P values are derived from two-sided Student’s t test ( d , f ), or log-rank test ( g ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Generated, CRISPR, Injection, In Vivo Imaging, RNA Sequencing Assay, Immunohistochemical staining, Staining, Standard Deviation, Derivative Assay

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a Single cell suspension was obtained from mouse spleen and expression of P2RX1 was determined in indicated immune cell types ( n = 3 per group, two independent experiments). Left dotted line indicates the mean of negative control (NC) (secondary antibody only), and right dotted line indicates the mean of Ly6G+ cells. b KPC cells were intrasplenically injected to seed livers of WT mice. A single cell suspension was obtained from liver metastases and adjacent liver tissues of WT mice at day 17. The frequency of CD45+P2RX1+ cells was determined by flow cytometry ( n = 4 per group, three independent experiments). c KPC cells were intrasplenically injected to seed livers of WT mice. Immune cells were enriched from single cell suspension of liver metastases and adjacent liver tissues at day 17. P2RX1 expression in the indicated immune cell types was determined by flow cytometry ( n = 4 per group, three independent experiments). d Representative images of H&E staining and immunofluorescence staining of P2RX1 (Green), Ly6G (Red) and DAPI (Blue) in KPC mice spontaneous liver metastases (representative results from six independent experiments). 50 μm scale bar for low power fields and 20 μm scale bar for high power fields. e , f H&E staining and immunofluorescence staining of P2RX1 (green), CD66b (red) and DAPI (blue) in a total of 20 clinical PDAC liver metastasis samples were performed. Representative images are shown in ( e ), and the percentages of P2RX1-CD66b+ cells are shown in ( f ). 50 μm scale bar for low power fields and 20 μm scale bar for high power fields. g , h KPC cells were intrasplenically injected to seed livers of BM chimeras: WT → WT, P2rx1 −/− → P2rx1 −/− , WT → P2rx1 −/− , and P2rx1 −/− → WT. Neutrophils were depleted in WT → P2rx1 −/− and P2rx1 −/− → WT mice by intraperitoneal injection of anti-Ly6G (clone 1A8) antibody. At day 17, liver metastases were analyzed by in vivo imaging ( g , n = 5 for WT → WT, P2rx1 −/− → P2rx1 −/− and WT → P2rx1 −/− groups, n = 4 for WT → P2rx1 −/− + anti-Ly6G, P2rx1 −/− → WT and P2rx1 −/− → WT + anti-Ly6G groups, two independent experiments), and representative images of liver metastatic samples were shown ( h ). Bars represent mean ± standard deviation in ( f , g ). P values are derived from two-sided Student’s t test ( c , f ), or one-way ANOVA and Tukey’s multiple comparisons test ( g ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Expressing, Negative Control, Injection, Flow Cytometry, Staining, Immunofluorescence, In Vivo Imaging, Standard Deviation, Derivative Assay

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a – g KPC cell was intrasplenically injected to seed livers of WT mice. Bone marrow (BM) and peripheral blood (PB) were obtained at day 17. Frequencies of neutrophils, P2RX1− neutrophils, and CXCR4+ neutrophils were determined by flow cytometry and quantitative results were shown ( n = 4 per group, three independent experiments). h Bone marrow neutrophils were isolated from WT mice and stimulated with indicated stimulus. RNA-seq were performed and Log 2 (FPKM+0.001) value of purinergic receptors were shown ( n = 1 per group). Bars represent mean ± standard deviation in ( e – g ). P values are derived from two-sided Student’s t test ( e – g ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Injection, Flow Cytometry, Isolation, RNA Sequencing Assay, Standard Deviation, Derivative Assay

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a , b KPC cells were intrasplenically injected to seed livers of WT and P2rx1 −/− mice. A single cell suspension was obtained from liver metastases at day 17. Then, P2RX1+ neutrophils were purified from WT mice, and P2rx1 −/− neutrophils were purified from P2rx1 −/− mice for RNA sequencing. The results of KEGG analysis are shown in ( a ), and comparative expression of genes is shown in ( b ) ( n = 1 per group). c Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with tumor conditioned medium (TCM). The ECAR and OCR were then measured by a Seahorse assay in ( c ), and PD-L1 and TNF-α were detected by RT-qPCR in ( d ) ( n = 4 per group, two independent experiments). Glc, glucose; O (ECAR), oligomycin; 2-DG, 2-deoxyglucose; O (OCR), oligomycin; F, FCCP (carbonyl cyanide 4-[trifluoromethoxy] phenylhydrazone); A & R, antimycin A and rotenone. Bars represent mean ± standard deviation in ( c , d ). P values are derived from two-sided Student’s t test ( d ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Injection, Purification, RNA Sequencing Assay, Expressing, Isolation, Quantitative RT-PCR, Standard Deviation, Derivative Assay

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a Gene set enrichment analysis comparing RNA-seq data of P2RX1+ neutrophils and P2rx1 −/− neutrophils based on Nrf2 target genes. The p value and normalized enrichment score (NES) were shown. b , c Single-cell suspensions were obtained from liver metastases of WT and P2rx1 −/− mice at day 17. Intracellular Nrf2 was stained and detected by flow cytometry ( b ) or laser scanning confocal microscopy ( c ) in WT P2RX1+ neutrophils and P2rx1 −/− neutrophils ( n = 4 per group, three independent experiments). The scale bar is 2.5 μm. d Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with LPS + IFN-γ in the presence or absence of a Nrf2 inhibitor. The ECAR was then measured by a Seahorse assay ( n = 4 per group, two independent experiments). Glc, glucose; O, oligomycin; 2-DG, 2-deoxyglucose. e Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with IL-4 in the presence or absence of a Nrf2 inhibitor. The OCR was then measured by a Seahorse assay ( n = 4 per group, two independent experiments). O, oligomycin; F, FCCP (carbonyl cyanide 4-[trifluoromethoxy] phenylhydrazone); A & R, antimycin A and rotenone. f Bone marrow neutrophils were isolated from WT or P2rx1 −/− mice and stimulated with LPS + IFN-γ and an inhibitor Nrf2 inhibitor. IL-1β and TNF-α were determined by RT-qPCR ( n = 4 per group, three independent experiments). Bars represent mean ± standard deviation in ( d – f ). P values are derived from permutation test ( a ), two-sided Student’s t test ( f ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: RNA Sequencing Assay, Staining, Flow Cytometry, Confocal Microscopy, Isolation, Quantitative RT-PCR, Standard Deviation, Derivative Assay

Journal: Nature Communications

Article Title: Identification of a subset of immunosuppressive P2RX1-negative neutrophils in pancreatic cancer liver metastasis

doi: 10.1038/s41467-020-20447-y

Figure Lengend Snippet: a A single cell suspension was obtained from liver metastases of WT and P2rx1 −/− mice at day 17. Flow cytometry was performed to detect the frequency of CD8+PD-1+ (upper) and Ly6G+PD-L1 + or Ly6G+PD-L1− (lower) cells. P2RX1 expression was further determined in Ly6G+PD-L1+ and Ly6G+PD-L1− cells from WT mice ( n = 4 per group, three independent experiments). b Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with tumor conditioned medium (TCM) or GM-CSF in the presence of a Nrf2 inhibitor or anti-GM-CSF neutralizing antibody. PD-L1 expression was detected by flow cytometry ( n = 4 per group, three independent experiments). c Integrative Genomics Viewer (IGV) was used to predict the two peaks that PD-L1 gene might be mediated by Nrf2 (upper). Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with GM-CSF. Binding of PD-L1 gene by Nrf2 was detected by ChIP-PCR ( n = 3 per group, two independent experiments). d Bone marrow neutrophils were isolated from WT and P2rx1 −/− mice and stimulated with GM-CSF. Intracellular ROS was detected by flow cytometry ( n = 4 per group, three independent experiments). e Antigen activated CTLs was co-cultured with GM-CSF primed WT or P2rx1 −/− neutrophils. Cell proliferation was analyzed with CSFE staining in the presence or absence of anti-PD-1 neutralizing antibody ( n = 4 per group, three independent experiments). f KPC cells were transfected with empty lentiviral vector (KPC-LV) or OVA (KPC-OVA). Antigen-activated CTLs were co-cultured with KPC-LV or KPC-OVA cells in the presence of GM-CSF-primed WT or P2rx1 −/− neutrophils. Cytotoxicity was determined in the presence or absence of anti-PD-1 neutralizing antibody by counting the number of PI+ cells ( n = 4 per group, three independent experiments). Bars represent mean ± standard deviation in ( f ). P values are derived from one-way ANOVA and Tukey’s multiple comparisons test ( f ). Source data are provided as a Source data file.

Article Snippet: For immunofluorescence staining, paraffin sections were dewaxed with gradient ethanol, steam heated for antigen retrieval in citrate-based buffer, blocked with PBS containing 10%BSA for 1 h, stained with anti-P2RX1 (Alomone, 1:200), and CD66b (Biologend, 1:1000), Ly6G (Biolegend, 1:1000), or citrullinated histone H3 (CitH3) (Alomone, 1:200) overnight and secondary antibody (Abcam, 1:1000) for 2 hr and finally mounted in DAPI-containing media (Vector Labs) for imaging on a laser scanning confocal microscope (Leica SP8 LAS X).

Techniques: Flow Cytometry, Expressing, Isolation, Binding Assay, Cell Culture, Staining, Transfection, Plasmid Preparation, Standard Deviation, Derivative Assay