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个体 Atg8 同源物在 - 诱导的层次化自噬中表现出独特的性质。

Individual Atg8 paralogs exhibit unique properties in -induced hierarchical autophagy.

机构信息

Department of Bacteriology I, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan.

出版信息

Autophagy. 2024 Nov;20(11):2584-2586. doi: 10.1080/15548627.2024.2375707. Epub 2024 Jul 11.

Abstract

Individual Atg8 (autophagy related 8) paralogs, comprising MAP1LC3A/LC3A, LC3B, LC3C, GABARAP, GABARAPL1 and GABARAPL2/GATE16, play a crucial role in canonical macroautophagy/autophagy. However, their functions remain unclear owing to functional redundancy. In a previous study, we reported that intracellular triggers hierarchical autophagy in response to bacterial infection. This process commences with the induction of conjugation of Atg8 paralogs (Atg8s) to single membranes (CASM), followed by CASM shedding and subsequent induction of xenophagy. In our recent study, we performed functional analysis of Atg8s during pneumococci-induced hierarchical autophagy. Our findings suggest that LC3A and GABARAPL1 are crucial for CASM induction, whereas GABARAPL2 and GABARAP play sequential roles in CASM shedding and subsequent induction of xenophagy, respectively.: Atg8: autophagy related 8; Atg8s: Atg8 paralogs; CASM: conjugation of Atg8s to single membranes; mpi: minutes post-infection; mpi: minutes post-infection; PcAV: pneumococci-containing autophagic vesicles; PcLV: LC3-associated phagosome (LAPosome)-like vacuole; PcV: pneumococci-containing vesicles; Sp: .

摘要

个体 Atg8(自噬相关 8)同源物,包括 MAP1LC3A/LC3A、LC3B、LC3C、GABARAP、GABARAPL1 和 GABARAPL2/GATE16,在经典的巨自噬/自噬中发挥关键作用。然而,由于功能冗余,它们的功能仍不清楚。在之前的研究中,我们报道了细胞内 触发细菌感染后的分层自噬。这个过程始于 Atg8 同源物(Atg8s)与单层膜(CASM)的缀合诱导,随后是 CASM 的脱落和随后的异噬诱导。在我们最近的研究中,我们对肺炎球菌诱导的分层自噬过程中的 Atg8s 进行了功能分析。我们的研究结果表明,LC3A 和 GABARAPL1 对于 CASM 的诱导至关重要,而 GABARAPL2 和 GABARAP 分别在 CASM 的脱落和随后的异噬诱导中发挥连续作用:Atg8:自噬相关 8;Atg8s:Atg8 同源物;CASM:Atg8s 与单层膜的缀合;mpi:感染后分钟;mpi:感染后分钟;PcAV:含有肺炎球菌的自噬小体;PcLV:LC3 相关噬菌小体(LAPosome)样空泡;PcV:含有肺炎球菌的小泡;Sp: 。

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本文引用的文献

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