4.7 Article

Targeting alveolar-specific succinate dehydrogenase A attenuates pulmonary inflammation during acute lung injury

期刊

FASEB JOURNAL
卷 35, 期 4, 页码 -

出版社

WILEY
DOI: 10.1096/fj.202002778R

关键词

ALI; alveolar epithelium; ARDS; HIF; inflammation; mechanical ventilation; SDHA; succinate

资金

  1. HHS | NIH | National Institute of Child Health and Human Development (NICHD) [K12HD068372]
  2. HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) [K08HL130586, R01HL133900, R01HL154720]
  3. Parker B Francis Foundation
  4. HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) [R01DK122796, R01DK109574]
  5. DOD | Defense Advanced Research Projects Agency (DARPA) [W81XWH2110032]

向作者/读者索取更多资源

Targeting alveolar-epithelial SDHA can dampen ALI through succinate-mediated stabilization of HIF1A. This has important implications for attenuating alveolar inflammation in patients suffering from ARDS.
Acute lung injury (ALI) is an inflammatory lung disease, which manifests itself in patients as acute respiratory distress syndrome (ARDS). Previous studies have implicated alveolar-epithelial succinate in ALI protection. Therefore, we hypothesized that targeting alveolar succinate dehydrogenase SDH A would result in elevated succinate levels and concomitant lung protection. Wild-type (WT) mice or transgenic mice with targeted alveolar-epithelial Sdha or hypoxia-inducible transcription factor Hif1a deletion were exposed to ALI induced by mechanical ventilation. Succinate metabolism was assessed in alveolar-epithelial via mass spectrometry as well as redox measurements and evaluation of lung injury. In WT mice, ALI induced by mechanical ventilation decreased SDHA activity and increased succinate in alveolar-epithelial. In vitro, cell-permeable succinate decreased epithelial inflammation during stretch injury. Mice with inducible alveolar-epithelial Sdha deletion (Sdha(loxp/loxp) SPC-CreER mice) revealed reduced lung inflammation, improved alveolar barrier function, and attenuated histologic injury. Consistent with a functional role of succinate to stabilize HIF, Sdha(loxp/loxp) SPC-CreER experienced enhanced Hif1a levels during hypoxia or ALI. Conversely, Hif1a(loxp/loxp) SPC-CreER showed increased inflammation with ALI induced by mechanical ventilation. Finally, wild-type mice treated with intra-tracheal dimethlysuccinate were protected during ALI. These data suggest that targeting alveolar-epithelial SDHA dampens ALI via succinate-mediated stabilization of HIF1A. Translational extensions of our studies implicate succinate treatment in attenuating alveolar inflammation in patients suffering from ARDS.

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