Department of Pediatrics, The First Affiliated Hospital of Nanhua University, Hengyang, Hunan People's Republic of China.
Autophagy. 2011 Oct;7(10):1242-4. doi: 10.4161/auto.7.10.16507. Epub 2011 Oct 1.
Autophagy and apoptosis are tightly regulated biological processes that are crucial for cell growth, development and tissue homeostasis. UVRAG (UV radiation resistance-associated gene), a mammalian homolog of yeast Vps38, activates the Beclin 1/PtdIns3KC3 (class III phosphatidylinositol-3-kinase) complex, which promotes autophagosome formation. Moreover, UVRAG promotes autophagosome maturation by recruiting class C Vps complexes (HOPS complexes) and Rab7 of the late endosome. We found that UVRAG has anti-apoptotic activity during tumor therapy through interactions with Bax. UVRAG inhibits Bax translocation from the cytosol to mitochondria during chemotherapy- or UV irradiation-induced apoptosis of human tumor cells. Moreover, deletion of the UVRAG C2 domain abolishes Bax binding and anti-apoptotic activity. These results suggest that, in addition to its previously recognized pro-autophagy activity in response to starvation, UVRAG has cytoprotective functions in the cytosol that control the localization of Bax in tumor cells exposed to apoptotic stimuli.
自噬和细胞凋亡是紧密调控的生物学过程,对于细胞生长、发育和组织稳态至关重要。UVRAG(紫外线辐射抗性相关基因)是酵母 Vps38 的哺乳动物同源物,可激活 Beclin 1/PtdIns3KC3(III 类磷脂酰肌醇 3-激酶)复合物,促进自噬体的形成。此外,UVRAG 通过募集类 C Vps 复合物(HOPS 复合物)和晚期内体的 Rab7 来促进自噬体成熟。我们发现 UVRAG 通过与 Bax 的相互作用在肿瘤治疗过程中具有抗凋亡活性。在人肿瘤细胞的化疗或紫外线照射诱导的细胞凋亡过程中,UVRAG 抑制 Bax 从细胞质向线粒体的易位。此外,删除 UVRAG 的 C2 结构域会消除 Bax 结合和抗凋亡活性。这些结果表明,除了其在饥饿时对自噬的先前公认的促进作用外,UVRAG 在细胞质中还具有保护细胞的功能,控制暴露于凋亡刺激的肿瘤细胞中 Bax 的定位。