Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
Curr Opin Cell Biol. 2010 Apr;22(2):199-205. doi: 10.1016/j.ceb.2009.11.004. Epub 2009 Dec 11.
Recently, DAP-kinase was identified as one of the essential regulators of autophagy, activated by signals such as cytokines and ER stress. DAP-kinase is a tumor suppressor that mediates several cell death pathways, such as apoptosis and programmed necrosis. Likewise, functional studies suggest that DAP-kinase may direct autophagy specifically towards autophagic cell death. Several recent studies have mapped DAP-kinase function to distinct stages in autophagy signaling. These include the Beclin-1/phosphatidylinositol 3-kinase (PI(3)K) complex, which is necessary for autophagosome formation, and an interaction with the LC3 binding protein, MAP1B, which may regulate vesicle trafficking. This review will summarize the functional and mechanistic studies that have linked DAP-kinase to the regulation of autophagy in general, and autophagic cell death, in particular.
最近,DAP-kinase 被鉴定为自噬的一个必要调节因子之一,它可以被细胞因子和 ER 应激等信号激活。DAP-kinase 是一种肿瘤抑制因子,介导多种细胞死亡途径,如细胞凋亡和程序性坏死。同样,功能研究表明 DAP-kinase 可能将自噬特异性地导向自噬性细胞死亡。最近的几项研究已经将 DAP-kinase 的功能映射到自噬信号的不同阶段。这些包括 Beclin-1/磷脂酰肌醇 3-激酶 (PI(3)K) 复合物,它是自噬体形成所必需的,以及与 LC3 结合蛋白 MAP1B 的相互作用,它可能调节囊泡运输。这篇综述将总结将 DAP-kinase 与自噬的调节联系起来的功能和机制研究,特别是与自噬性细胞死亡的关系。