车站3
磷酸化
细胞生物学
线粒体
酪氨酸
酪氨酸磷酸化
生物
丝氨酸
功能(生物学)
转录因子
突变体
化学
生物化学
基因
作者
Joanna Węgrzyn,Ramesh Potla,Yong-Joon Chwae,Naresh Babu V. Sepuri,Qifang Zhang,Thomas Koeck,Marta Derecka,Karol Szczepanek,Magdalena Szeląg,Agnieszka Górnicka,Akira Moh,Shadi Moghaddas,Qun Chen,Santha Bobbili,Joanna Cichy,Józef Dulak,Darren P. Baker,Alan Wolfman,Dennis J. Stuehr,Medhat O. Hassan
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2009-01-08
卷期号:323 (5915): 793-797
被引量:993
标识
DOI:10.1126/science.1164551
摘要
Cytokines such as interleukin-6 induce tyrosine and serine phosphorylation of Stat3 that results in activation of Stat3-responsive genes. We provide evidence that Stat3 is present in the mitochondria of cultured cells and primary tissues, including the liver and heart. In Stat3 â/â cells, the activities of complexes I and II of the electron transport chain (ETC) were significantly decreased. We identified Stat3 mutants that selectively restored the protein's function as a transcription factor or its functions within the ETC. In mice that do not express Stat3 in the heart, there were also selective defects in the activities of complexes I and II of the ETC. These data indicate that Stat3 is required for optimal function of the ETC, which may allow it to orchestrate responses to cellular homeostasis.
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