normal human lung fibroblast Search Results


99
ATCC primary human lung fibroblasts hlfs
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Primary Human Lung Fibroblasts Hlfs, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC human lung fibroblasts
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Human Lung Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Lonza primary human lung fibroblasts
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Primary Human Lung Fibroblasts, supplied by Lonza, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Coriell Institute for Medical Research normal human lung fibroblasts (1522)
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Normal Human Lung Fibroblasts (1522), supplied by Coriell Institute for Medical Research, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
JCRB Cell Bank human normal lung fibroblasts mrc-5
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Human Normal Lung Fibroblasts Mrc 5, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
BioWhittaker Molecular Applications lung fibroblasts (nhlf 5975
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Lung Fibroblasts (Nhlf 5975, supplied by BioWhittaker Molecular Applications, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JCRB Cell Bank normal human lung fibroblasts hfliii
A Human lung smooth muscle cells (HLSMCs), lung <t>fibroblasts</t> <t>(HLFs),</t> and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.
Normal Human Lung Fibroblasts Hfliii, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Lonza normal human lung fibroblasts nhlf lot#0000580583
Cell donor and drug stimulation: Time-course pixel intensity data show the effects on fibrin degradation of several different stimulants, with <t>NHLF</t> cells on the left and diseased IPF cells on the right. The upper pixel intensity graphs have no TGF-β1 (a and e) while the lower graphs contain 2 ng/ml TGF-β1 (b and f). Sigmoid fits were used to determine 50% degradation time (c, d, g and h) from the above pixel intensity graphs. Dotted lines show mean value from control conditions for comparison. (Statistical significance P < 0.01 by two-way ANOVA: As the positive control, plasmin was excluded from ANOVA. ‡ = P < 0.01; ad, be = P < 0.05; ac, fg, fh = P < 0.1 by post-hoc Tukey test. N = 4 for all conditions)
Normal Human Lung Fibroblasts Nhlf Lot#0000580583, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Lonza normal human lung 4 fibroblasts
Cell donor and drug stimulation: Time-course pixel intensity data show the effects on fibrin degradation of several different stimulants, with <t>NHLF</t> cells on the left and diseased IPF cells on the right. The upper pixel intensity graphs have no TGF-β1 (a and e) while the lower graphs contain 2 ng/ml TGF-β1 (b and f). Sigmoid fits were used to determine 50% degradation time (c, d, g and h) from the above pixel intensity graphs. Dotted lines show mean value from control conditions for comparison. (Statistical significance P < 0.01 by two-way ANOVA: As the positive control, plasmin was excluded from ANOVA. ‡ = P < 0.01; ad, be = P < 0.05; ac, fg, fh = P < 0.1 by post-hoc Tukey test. N = 4 for all conditions)
Normal Human Lung 4 Fibroblasts, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JCRB Cell Bank normal human lung fibroblasts hfl-iii
Cell donor and drug stimulation: Time-course pixel intensity data show the effects on fibrin degradation of several different stimulants, with <t>NHLF</t> cells on the left and diseased IPF cells on the right. The upper pixel intensity graphs have no TGF-β1 (a and e) while the lower graphs contain 2 ng/ml TGF-β1 (b and f). Sigmoid fits were used to determine 50% degradation time (c, d, g and h) from the above pixel intensity graphs. Dotted lines show mean value from control conditions for comparison. (Statistical significance P < 0.01 by two-way ANOVA: As the positive control, plasmin was excluded from ANOVA. ‡ = P < 0.01; ad, be = P < 0.05; ac, fg, fh = P < 0.1 by post-hoc Tukey test. N = 4 for all conditions)
Normal Human Lung Fibroblasts Hfl Iii, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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AddexBio Inc normal human lung fibroblast hel299 cell line
Viability of the normal human lung fibroblast <t>HEL299</t> cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.
Normal Human Lung Fibroblast Hel299 Cell Line, supplied by AddexBio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Lonza microvesicles derived normal human lung fibroblasts (nhlf mv
(A) Schematic view of the ex vivo human lung preparation as well as lung perfusion and ventilation protocol used for the experiments. (B) Electron microscopy image of human mesenchymal stem cells (MSC) constitutively releasing <t>microvesicles</t> (MV) after 48 h of serum starvation. Black arrows designate MV, which appear as spheroids budding off the plasma membrane. Insert shows a homogenous collection of MSC MV, which is 50 to 200 nm in size. (C) Protein concentration of 100 μL of MSC MV. Data represent the median of 24 samples of MSC MV. (D) Western Blot showing the expression of the membrane receptor CD44 by MSC MV. CD44 plays an important role in MSC MV internalization into the host cell. PCR showing the expression of Ang1 mRNA by RT-PCR.
Microvesicles Derived Normal Human Lung Fibroblasts (Nhlf Mv, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


A Human lung smooth muscle cells (HLSMCs), lung fibroblasts (HLFs), and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.

Journal: Cell Death Discovery

Article Title: Trifluoperazine causes mast cell apoptosis through a secretory granule-mediated pathway

doi: 10.1038/s41420-026-03122-x

Figure Lengend Snippet: A Human lung smooth muscle cells (HLSMCs), lung fibroblasts (HLFs), and small airway epithelial cells (HSAECs) were treated with TFP at the indicated concentrations for 24 h. Human peripheral blood eosinophils and neutrophils were treated with TFP for 2 h. Cell viability was assessed by staining the cells with Annexin V (AnnV) and DRAQ7. Viable cells, AnnV − DRAQ7 − ; apoptotic cells, AnnV + DRAQ7 − ; necrotic/late apoptotic cells, AnnV + DRAQ7 + . HSAECs, n = 6 from three independent experiments; HLSMCs, eosinophils, neutrophils, n = 4 from four independent experiments; HLFs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA for HLSMCs, HLFs; Kruskal-Wallis for HSAECs; Friedman test for eosinophils, neutrophils). B – C Bone marrow-derived MCs (BMMCs) and peritoneal cell-derived MCs (PCMCs) treated under the same conditions as in ( A ) for 24 h. BMMCs, n = 5 from two independent experiments; PCMCs, n = 3 from one individual experiment representative of three independent experiments (One-way ANOVA). Untreated (control) cells were used for statistical comparisons to all other groups in all figures. The bar charts show mean values + SEM or median + interquartile range. * P < 0.05; ** P < 0 .01; **** P < 0.0001. D Effect of TFP on DNA degradation. MCs were preincubated with bafilomycin A1 (Baf A1) (20 nM) for 2 h followed by treatment with TFP (10 μΜ) for 2 h. DNA was extracted from MCs and fragmentation was assessed by agarose gel electrophoresis. St standard marker.

Article Snippet: Primary human lung fibroblasts (HLFs) (PCS-201-013) and primary human lung smooth muscle cells (HLSMCs)(PCS-130-010) were obtained from American Type Culture Collection (ATCC, Manassas, VA) and cultured following the manufacturer’s instructions.

Techniques: Staining, Derivative Assay, Control, Agarose Gel Electrophoresis, Marker

Cell donor and drug stimulation: Time-course pixel intensity data show the effects on fibrin degradation of several different stimulants, with NHLF cells on the left and diseased IPF cells on the right. The upper pixel intensity graphs have no TGF-β1 (a and e) while the lower graphs contain 2 ng/ml TGF-β1 (b and f). Sigmoid fits were used to determine 50% degradation time (c, d, g and h) from the above pixel intensity graphs. Dotted lines show mean value from control conditions for comparison. (Statistical significance P < 0.01 by two-way ANOVA: As the positive control, plasmin was excluded from ANOVA. ‡ = P < 0.01; ad, be = P < 0.05; ac, fg, fh = P < 0.1 by post-hoc Tukey test. N = 4 for all conditions)

Journal: Biofabrication

Article Title: Aqueous two-phase deposition and fibrinolysis of fibroblast-laden fibrin micro-scaffolds

doi: 10.1088/1758-5090/abdb85

Figure Lengend Snippet: Cell donor and drug stimulation: Time-course pixel intensity data show the effects on fibrin degradation of several different stimulants, with NHLF cells on the left and diseased IPF cells on the right. The upper pixel intensity graphs have no TGF-β1 (a and e) while the lower graphs contain 2 ng/ml TGF-β1 (b and f). Sigmoid fits were used to determine 50% degradation time (c, d, g and h) from the above pixel intensity graphs. Dotted lines show mean value from control conditions for comparison. (Statistical significance P < 0.01 by two-way ANOVA: As the positive control, plasmin was excluded from ANOVA. ‡ = P < 0.01; ad, be = P < 0.05; ac, fg, fh = P < 0.1 by post-hoc Tukey test. N = 4 for all conditions)

Article Snippet: Cell preparation Normal human lung fibroblasts (NHLF lot#0000580583; Lonza) from a 79 year old female with a history of smoking, and idiopathic pulmonary fibrosis fibroblasts (IPF lot#0000627840; Lonza) from a 52 year old male were cultured in fibroblast growth media (FGM; Lonza).

Techniques: Control, Comparison, Positive Control

Viability of the normal human lung fibroblast HEL299 cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.

Journal: Nanoscale Advances

Article Title: Drug delivery with a pH-sensitive star-like dextran-graft polyacrylamide copolymer

doi: 10.1039/d2na00353h

Figure Lengend Snippet: Viability of the normal human lung fibroblast HEL299 cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.

Article Snippet: Lung carcinoma human A549 and normal human lung fibroblast HEL299 cell lines were purchased from AddexBio Technologies (San Diego, CA, USA).

Techniques:

IC 50 of free drugs and drug-loaded D- g -PAAan nanoparticles on  HEL299  cell viability

Journal: Nanoscale Advances

Article Title: Drug delivery with a pH-sensitive star-like dextran-graft polyacrylamide copolymer

doi: 10.1039/d2na00353h

Figure Lengend Snippet: IC 50 of free drugs and drug-loaded D- g -PAAan nanoparticles on HEL299 cell viability

Article Snippet: Lung carcinoma human A549 and normal human lung fibroblast HEL299 cell lines were purchased from AddexBio Technologies (San Diego, CA, USA).

Techniques:

(A) Schematic view of the ex vivo human lung preparation as well as lung perfusion and ventilation protocol used for the experiments. (B) Electron microscopy image of human mesenchymal stem cells (MSC) constitutively releasing microvesicles (MV) after 48 h of serum starvation. Black arrows designate MV, which appear as spheroids budding off the plasma membrane. Insert shows a homogenous collection of MSC MV, which is 50 to 200 nm in size. (C) Protein concentration of 100 μL of MSC MV. Data represent the median of 24 samples of MSC MV. (D) Western Blot showing the expression of the membrane receptor CD44 by MSC MV. CD44 plays an important role in MSC MV internalization into the host cell. PCR showing the expression of Ang1 mRNA by RT-PCR.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Article Title: Microvesicles Derived From Human Mesenchymal Stem Cells Restore Alveolar Fluid Clearance in Human Lungs Rejected for Transplantation

doi: 10.1111/ajt.13271

Figure Lengend Snippet: (A) Schematic view of the ex vivo human lung preparation as well as lung perfusion and ventilation protocol used for the experiments. (B) Electron microscopy image of human mesenchymal stem cells (MSC) constitutively releasing microvesicles (MV) after 48 h of serum starvation. Black arrows designate MV, which appear as spheroids budding off the plasma membrane. Insert shows a homogenous collection of MSC MV, which is 50 to 200 nm in size. (C) Protein concentration of 100 μL of MSC MV. Data represent the median of 24 samples of MSC MV. (D) Western Blot showing the expression of the membrane receptor CD44 by MSC MV. CD44 plays an important role in MSC MV internalization into the host cell. PCR showing the expression of Ang1 mRNA by RT-PCR.

Article Snippet: If 0 microvesicles derived from normal human lung fibroblasts (NHLF MV, Lonza, Basel, Switzerland) was administered into the perfusate.

Techniques: Ex Vivo, Electron Microscopy, Protein Concentration, Western Blot, Expressing, Reverse Transcription Polymerase Chain Reaction

Administration of MSC MV significantly improved AFC in a dose-dependent manner compared to the Control (Perfusion only) at T6. Administration of NHLF MV as a cellular control had no effect on AFC compared to the Control at T6. Inhibition of CD44 with a neutralizing Ab significantly reduced the therapeutic effect of MSC MV 200 μL, whereas administration of IgG control with MSC MV 200 μL had no significant effect. Data are presented as mean ± SD, N = 4-6 per group. *p significant by ANOVA vs. T0, †p significant by ANOVA versus T6 Perfusion Only, ‡p significant by ANOVA versus T6 MSC MV 200 μL. Abbreviations: Ab, antibody; AFC, alveolar fluid clearance; MSC, mesenchymal stem cells; MV, microvesicles; NHLF, normal human lung fibroblast.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Article Title: Microvesicles Derived From Human Mesenchymal Stem Cells Restore Alveolar Fluid Clearance in Human Lungs Rejected for Transplantation

doi: 10.1111/ajt.13271

Figure Lengend Snippet: Administration of MSC MV significantly improved AFC in a dose-dependent manner compared to the Control (Perfusion only) at T6. Administration of NHLF MV as a cellular control had no effect on AFC compared to the Control at T6. Inhibition of CD44 with a neutralizing Ab significantly reduced the therapeutic effect of MSC MV 200 μL, whereas administration of IgG control with MSC MV 200 μL had no significant effect. Data are presented as mean ± SD, N = 4-6 per group. *p significant by ANOVA vs. T0, †p significant by ANOVA versus T6 Perfusion Only, ‡p significant by ANOVA versus T6 MSC MV 200 μL. Abbreviations: Ab, antibody; AFC, alveolar fluid clearance; MSC, mesenchymal stem cells; MV, microvesicles; NHLF, normal human lung fibroblast.

Article Snippet: If 0 microvesicles derived from normal human lung fibroblasts (NHLF MV, Lonza, Basel, Switzerland) was administered into the perfusate.

Techniques: Inhibition

Effect of microvesicles derived from human mesenchymal stem cells on lung (A) tracheal pressure and (B) compliance. Perfusion with ventilation significantly increased tracheal pressure at T6. Administration of either doses of MSC MV reduced the tracheal pressure to baseline, increasing the compliance of the lung compared to T0. Data are presented as mean ± SD, N = 4–6 per group. Abbreviations: Ab, antibody; MSC, mesenchymal stem cells; MV, microvesicles.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Article Title: Microvesicles Derived From Human Mesenchymal Stem Cells Restore Alveolar Fluid Clearance in Human Lungs Rejected for Transplantation

doi: 10.1111/ajt.13271

Figure Lengend Snippet: Effect of microvesicles derived from human mesenchymal stem cells on lung (A) tracheal pressure and (B) compliance. Perfusion with ventilation significantly increased tracheal pressure at T6. Administration of either doses of MSC MV reduced the tracheal pressure to baseline, increasing the compliance of the lung compared to T0. Data are presented as mean ± SD, N = 4–6 per group. Abbreviations: Ab, antibody; MSC, mesenchymal stem cells; MV, microvesicles.

Article Snippet: If 0 microvesicles derived from normal human lung fibroblasts (NHLF MV, Lonza, Basel, Switzerland) was administered into the perfusate.

Techniques: Derivative Assay

(A) Compared to T0 and the Control (Perfusion only) at T6, administration of either dose of MSC MV reduced the perfusate pH to more physiological levels. (B) In addition, there was a strong correlation with the change in pH with the AFC, perhaps suggesting that there were increased metabolic activity in the lungs that received MSC MV. Spearman’s rank correlation coefficient, rs = −0.7657. Data are presented as mean ± SD, N = 4–6 per group. *p significant by ANOVA versus T0, †p significant by ANOVA versus Perfusion Group at the corresponding time point. Abbreviations: MSC, mesenchymal stem cells; MV, microvesicles; NHLF, normal human lung fibroblast.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Article Title: Microvesicles Derived From Human Mesenchymal Stem Cells Restore Alveolar Fluid Clearance in Human Lungs Rejected for Transplantation

doi: 10.1111/ajt.13271

Figure Lengend Snippet: (A) Compared to T0 and the Control (Perfusion only) at T6, administration of either dose of MSC MV reduced the perfusate pH to more physiological levels. (B) In addition, there was a strong correlation with the change in pH with the AFC, perhaps suggesting that there were increased metabolic activity in the lungs that received MSC MV. Spearman’s rank correlation coefficient, rs = −0.7657. Data are presented as mean ± SD, N = 4–6 per group. *p significant by ANOVA versus T0, †p significant by ANOVA versus Perfusion Group at the corresponding time point. Abbreviations: MSC, mesenchymal stem cells; MV, microvesicles; NHLF, normal human lung fibroblast.

Article Snippet: If 0 microvesicles derived from normal human lung fibroblasts (NHLF MV, Lonza, Basel, Switzerland) was administered into the perfusate.

Techniques: Activity Assay