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Image Search Results
Journal: bioRxiv
Article Title: Mitochondrial One-Carbon Metabolism is Required for TGF-β-Induced Glycine Synthesis and Collagen Protein Production
doi: 10.1101/2023.11.07.566074
Figure Lengend Snippet: (A) Histological analysis of MTHFD2 protein expression in fibrotic and nonfibrotic areas of paraffin-embedded lung sections from a patient with idiopathic pulmonary fibrosis. (B) Western blot analysis of MTHFD2 protein expression in mouse lung tissue either prior to, or 14 or 21 days after bleomycin instillation. (C) Pearson’s correlation of MTHFD2 mRNA level and forced vital capacity before bronchodilator (FVC-pre-BD) as percentage of what was predicted for each patient. Data is from GSE32537. (D) Western blot analysis of collagen and α-smooth muscle actin protein expression in normal human lung fibroblasts (NHLFs) treated with TGF-β for the indicated intervals in the presence or absence of DS18561882 (5μM). (E-G) Analysis of cellular (E) glycine, (F) serine, and (G) proline in NHLFs after labeling with 2,3,3-D3-Serine in the presence or absence of TGF-β and DS18561882. (H) Relative levels of media formate content in NHLFs treated with TGF-β or left untreated in the presence or absence of DS18561882. (I) Representative coronal microCT images of mice prior to bleomycin instillation (Day 0), 7 days after bleomycin instillation (Day 7), and 14 days after bleomycin instillation (Day 14). Mice began receiving DS18561882 (125 mg/kg) or vehicle 8 days after bleomycin instillation. (J) Quantification of aerated lung volumes from microCT-scanned mice treated as in (I) (mean ± SEM). (K) Histological analysis of mouse lung tissue on day 21 after bleomycin instillation. Beginning on day 8, mice received daily IP injections of either DS18561882 or vehicle. (L) Hydroxyproline content of mouse lungs on day 21 after bleomycin or vehicle (saline) instillation. Beginning on day 8, mice received either DS18561882 or vehicle IP, daily (mean ± SEM). * P <0.05, ** P <0.01, *** P <0.001.
Article Snippet: Available clinical data was correlated to individual gene expression profiles using
Techniques: Expressing, Western Blot, Labeling, Saline