The Institute for Immunology, University of California, Irvine, CA 92697-3900, USA.
Curr Opin Immunol. 2010 Jun;22(3):321-5. doi: 10.1016/j.coi.2010.03.005. Epub 2010 Apr 12.
Autophagy, an ancient cellular response where autophagic vacuoles are formed within the cytosol, is induced in response to a variety of cellular insults, including growth factor or nutrient withdrawal, organelle damage, and misfolded proteins. Autophagy is rapidly induced in T lymphocytes following antigenic stimulation and blockade of autophagic signaling greatly reduces T cell clonal expansion, suggesting that autophagy is primarily involved in promoting T cell survival. In contrast, a recently identified negative feedback loop involving FADD and caspase-8 limits the level of autophagy in T cells. Failure to activate caspase-8 during T cell mitogenesis leads to hyperactive autophagy and cellular death through a programmed necrotic mechanism. These findings suggest that crosstalk between these cellular processes is essential for T cell activation and homeostasis.
自噬是一种古老的细胞反应,其中自噬小泡在细胞质内形成,是对多种细胞应激的反应,包括生长因子或营养物质的剥夺、细胞器损伤和错误折叠的蛋白质。抗原刺激后,T 淋巴细胞中自噬迅速被诱导,而自噬信号的阻断大大减少了 T 细胞克隆扩增,这表明自噬主要参与促进 T 细胞存活。相比之下,最近发现的涉及 FADD 和 caspase-8 的负反馈环限制了 T 细胞中的自噬水平。在 T 细胞有丝分裂过程中未能激活 caspase-8 会导致过度活跃的自噬和通过程序性坏死机制的细胞死亡。这些发现表明这些细胞过程之间的相互作用对于 T 细胞的激活和稳态是必不可少的。