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ATG 连接系统对于内自噬体膜的降解很重要。

The ATG conjugation systems are important for degradation of the inner autophagosomal membrane.

机构信息

Department of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.

Research Center for Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.

出版信息

Science. 2016 Nov 25;354(6315):1036-1041. doi: 10.1126/science.aaf6136. Epub 2016 Oct 20.

Abstract

In macroautophagy, cytoplasmic contents are sequestered into the double-membrane autophagosome, which fuses with the lysosome to become the autolysosome. It has been thought that the autophagy-related (ATG) conjugation systems are required for autophagosome formation. Here, we found that autophagosomal soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) syntaxin 17-positive autophagosome-like structures could be generated even in the absence of the ATG conjugation systems, although at a reduced rate. These syntaxin 17-positive structures could further fuse with lysosomes, but degradation of the inner autophagosomal membrane was significantly delayed. Accordingly, autophagic activity in ATG conjugation-deficient cells was strongly suppressed. We suggest that the ATG conjugation systems, which are likely required for the closure (i.e., fission) of the autophagosomal edge, are not absolutely essential for autolysosome formation but are important for efficient degradation of the inner autophagosomal membrane.

摘要

在巨自噬中,细胞质内容物被隔离到双层自噬体中,自噬体与溶酶体融合形成自溶酶体。人们一直认为自噬相关(ATG)连接系统是自噬体形成所必需的。在这里,我们发现即使在没有 ATG 连接系统的情况下,也可以产生自噬体可溶性 N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)突触蛋白 17 阳性的自噬体样结构,但速度较慢。这些突触蛋白 17 阳性结构可以进一步与溶酶体融合,但内自噬体膜的降解明显延迟。因此,ATG 连接缺陷细胞中的自噬活性受到强烈抑制。我们认为,ATG 连接系统可能是自噬体边缘关闭(即分裂)所必需的,但对于自溶酶体的形成并不是绝对必要的,而是对于内自噬体膜的有效降解是重要的。

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