McKnight Nicole C, Zhenyu Yue
Department of Neurology and Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Curr Pathobiol Rep. 2013 Dec 1;1(4):231-238. doi: 10.1007/s40139-013-0028-5.
Autophagy is a cell 'self-digestion' pathway involving the synthesis, trafficking and delivery of autophagosomes to lysosomes for degradation. Beclin 1 is a core component of the class III phosphatidylinositol 3-kinase (PI3K-III) complex, which plays an important role in membrane trafficking and restructuring involved in autophagy, endocytosis, cytokinesis and phagocytosis. To date Beclin 1 has largely been characterized in the context of autophagy; it modulates the lipid kinase activity of PI3K-III catalytic unit VPS34, which generates phosphatidylinositol 3-phosphate (PI(3)P), enabling the recruitment of a number of autophagy proteins involved in the nucleation of the autophagosome. Beclin 1 seems to function as an adaptor for recruiting multiple proteins that modulate VPS34. The recent identification of Beclin 1 protein modifications has shed light on its regulation in autophagy, and the discovery of non-autophagy functions of Beclin 1 has expanded our view of Beclin 1's involvement in tissue homeostasis and human diseases.
自噬是一种细胞“自我消化”途径,涉及自噬体的合成、运输以及将其递送至溶酶体进行降解。Beclin 1是III类磷脂酰肌醇3激酶(PI3K-III)复合物的核心组分,该复合物在参与自噬、胞吞作用、胞质分裂和吞噬作用的膜运输及重塑过程中发挥重要作用。迄今为止,Beclin 1主要是在自噬背景下得以表征;它调节PI3K-III催化亚基VPS34的脂质激酶活性,VPS34可生成磷脂酰肌醇3-磷酸(PI(3)P),从而使得一些参与自噬体成核的自噬蛋白得以募集。Beclin 1似乎作为一种衔接蛋白,用于募集多种调节VPS34的蛋白质。最近对Beclin 1蛋白修饰的鉴定揭示了其在自噬中的调节机制,并且Beclin 1非自噬功能的发现拓展了我们对Beclin 1参与组织稳态及人类疾病的认识。