丙酮酸激酶
巴基斯坦卢比
糖酵解
乳酸脱氢酶A
免疫学
医学
内科学
新陈代谢
作者
Cheryl van de Wetering,Allison M. Manuel,Mona Sharafi,Reem Aboushousha,Xi Qian,Cuixia Erickson,Maximilian B. MacPherson,Garrett J. Chan,Ian M. Adcock,Nazanin Zounemat Kermani,Florence Schleich,Renaud Louis,Eric Bohrnsen,Angelo D’Alessandro,Emiel F.�M. Wouters,Niki L. Reynaert,Jianing Li,C. Roland Wolf,Colin J. Henderson,Lennart K. A. Lundblad
出处
期刊:Redox biology
[Elsevier BV]
日期:2021-10-04
卷期号:47: 102160-102160
被引量:28
标识
DOI:10.1016/j.redox.2021.102160
摘要
Interleukin-1-dependent increases in glycolysis promote allergic airways disease in mice and disruption of pyruvate kinase M2 (PKM2) activity is critical herein. Glutathione-S-transferase P (GSTP) has been implicated in asthma pathogenesis and regulates the oxidation state of proteins via S-glutathionylation. We addressed whether GSTP-dependent S-glutathionylation promotes allergic airways disease by promoting glycolytic reprogramming and whether it involves the disruption of PKM2.
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