自噬参与结核杆菌感染免疫应答调控的研究进展

Autophagy participating in inhibiting mycobacterium tuberculosis survival in infected macrophages

  • 摘要: 自噬是将细胞溶质中功能不全的蛋白质和细胞器运输到溶酶体进行降解的一种途径或方式,在生物进化中十分保守,在维持细胞内稳态方面发挥了重要作用。巨噬细胞是结核菌感染的主要靶细胞,也是机体感染结核杆菌后最早起作用的细胞。自噬能直接清除感染巨噬细胞的结核分枝杆菌,同时,结核分枝杆菌可以干扰自噬体与溶酶体的融合,隐藏在自噬体的双层膜结构中逃避自噬对其杀灭,从而在宿主细胞内长期存活并繁殖。自噬与结核病的发生、发展密切相关,自噬的研究对提高结核病的治疗和预后效果具有重要的意义。

     

    Abstract: Autophagy is an evolutionarily conserved process which plays a vital role in maintaining cytoplasmic homeostasis by degrading damaged organelles or misfolded proteins in phagolysosome. The anti-mycobacterial immunology is mainly dependent on macrophages which belong to the fi rst line of anti-mycobacterial immune defense system. Although the induction of autophagy suppresses intracellular survival of mycobacterial, the bacteria are capable of surviving and persisting within host macrophages because of its repertoire of evading the host immune response, and mycobacterial can limit the maturation of mycobacterial phagosomes to escape degradation by lysosomal hydrolases. Autophagy is closely related with mycobacterial tuberculosis. The researches on autophagy reveal a novel direction in regulating autophagy-mediated mycobacterial elimination, and provide potential targets for clinical treatment.

     

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