Proline biosynthesis is a vent for TGFβ-induced mitochondrial redox stress Journal Article


Authors: Schwörer, S.; Berisa, M.; Violante, S.; Qin, W.; Zhu, J.; Hendrickson, R. C.; Cross, J. R.; Thompson, C. B.
Article Title: Proline biosynthesis is a vent for TGFβ-induced mitochondrial redox stress
Abstract: The production and secretion of matrix proteins upon stimulation of fibroblasts by transforming growth factor-beta (TGFβ) play a critical role in wound healing. How TGFβ supports the bioenergetic cost of matrix protein synthesis is not fully understood. Here, we show that TGFβ promotes protein translation at least in part by increasing the mitochondrial oxidation of glucose and glutamine carbons to support the bioenergetic demand of translation. Surprisingly, we found that in addition to stimulating the entry of glucose and glutamine carbon into the TCA cycle, TGFβ induced the biosynthesis of proline from glutamine in a Smad4-dependent fashion. Metabolic manipulations that increased mitochondrial redox generation promoted proline biosynthesis, while reducing mitochondrial redox potential and/or ATP synthesis impaired proline biosynthesis. Thus, proline biosynthesis acts as a redox vent, preventing the TGFβ-induced increase in mitochondrial glucose and glutamine catabolism from generating damaging reactive oxygen species (ROS) when TCA cycle activity exceeds the ability of oxidative phosphorylation to convert mitochondrial redox potential into ATP. In turn, the enhanced synthesis of proline supports TGFβ-induced production of matrix proteins. © 2020 The Authors
Keywords: controlled study; human cell; nonhuman; dna synthesis; animal cell; mouse; metabolism; animal tissue; transforming growth factor beta; animal experiment; animal model; fibrosis; collagen; reactive oxygen metabolite; glucose; adenosine triphosphate; glycolysis; oxidative phosphorylation; matrix protein; glutamine; metabolic regulation; proline; citric acid cycle; mitochondrial respiration; smad4 protein; amino acid synthesis; tgfΒ; redox stress; human; priority journal; article; oxidation reduction potential
Journal Title: EMBO Journal
Volume: 39
Issue: 8
ISSN: 0261-4189
Publisher: Wiley Blackwell  
Date Published: 2020-04-15
Start Page: e103334
Language: English
DOI: 10.15252/embj.2019103334
PUBMED: 32134147
PROVIDER: scopus
PMCID: PMC7156964
DOI/URL:
Notes: Article -- Source: Scopus
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MSK Authors
  1. Weige Qin
    10 Qin
  2. Justin Robert Cross
    111 Cross
  3. Craig Bernie Thompson
    153 Thompson
  4. Jiajun Zhu
    6 Zhu
  5. Mirela Berisa
    6 Berisa