Bourke Lauren T, Knight Richard A, Latchman David S, Stephanou Anastasis, McCormick James
Medical Molecular Biology Unit; University College London; London, UK.
Birkbeck College; University of London; London, UK.
JAKSTAT. 2013 Oct 1;2(4):e25666. doi: 10.4161/jkst.25666. Epub 2013 Jul 15.
The signal transducer and activator of transcription (STAT) proteins are latent transcription factors that have been shown to be involved in cell proliferation, development, apoptosis, and autophagy. STAT proteins undergo activation by phosphorylation at tyrosine 701 and serine 727 where they translocate to the nucleus to regulate gene expression. STAT1 has been shown to be involved in promoting apoptotic cell death in response to cardiac ischemia/reperfusion and has recently been shown by our laboratory to be involved in negatively regulating autophagy. These processes are thought to promote cell death and restrict cell survival leading to the generation of an infarct. Here we present data that shows STAT1 localizes to the mitochondria and co-immunoprecipitates with LC3. Furthermore, electron microscopy studies also reveal mitochondria from ex vivo I/R treated hearts of STAT1KO mice contained within a double membrane autophagosome indicating that STAT1 may be involved in negatively regulating mitophagy. This is the first description of STAT1 being localized to the mitochondria and also having a role in mitophagy.
信号转导与转录激活因子(STAT)蛋白是潜在的转录因子,已被证明参与细胞增殖、发育、凋亡和自噬过程。STAT蛋白通过酪氨酸701和丝氨酸727位点的磷酸化而被激活,随后易位至细胞核以调节基因表达。STAT1已被证明在心脏缺血/再灌注后促进凋亡性细胞死亡,并且最近我们实验室发现它还参与负向调节自噬。这些过程被认为会促进细胞死亡并限制细胞存活,从而导致梗死灶的形成。在此,我们展示的数据表明STAT1定位于线粒体并与LC3进行共免疫沉淀。此外,电子显微镜研究还揭示,STAT1基因敲除小鼠经离体缺血/再灌注处理的心脏中的线粒体包含在双膜自噬小体内,这表明STAT1可能参与负向调节线粒体自噬。这是首次描述STAT1定位于线粒体并在线粒体自噬中发挥作用。