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内质网自噬与人类疾病。

ER-phagy and human diseases.

机构信息

Institute of Human Genetics, University Hospital Jena, Friedrich-Schiller-Universität Jena, Jena, Germany.

Institute of Biochemistry II, Goethe University School of Medicine, Frankfurt, Germany.

出版信息

Cell Death Differ. 2020 Mar;27(3):833-842. doi: 10.1038/s41418-019-0444-0. Epub 2019 Oct 28.

Abstract

Autophagy regulates the degradation of unnecessary or dysfunctional cellular components. This catabolic process requires the formation of a double-membrane vesicle, the autophagosome, that engulfs the cytosolic material and delivers it to the lysosome. Substrate specificity is achieved by autophagy receptors, which are characterized by the presence of at least one LC3-interaction region (LIR) or GABARAP-interaction motif (GIM). Only recently, several receptors that mediate the specific degradation of endoplasmic reticulum (ER) components via autophagy have been identified (the process known as ER-phagy or reticulophagy). Here, we give an update on the current knowledge about the role of ER-phagy receptors in health and disease.

摘要

自噬调节细胞内不必要或功能失调的成分的降解。这个分解代谢过程需要形成一个双层膜囊泡,即自噬体,它吞噬细胞质物质并将其递送至溶酶体。通过自噬受体实现底物特异性,其特征是至少存在一个 LC3 相互作用区域(LIR)或 GABARAP 相互作用基序(GIM)。直到最近,才鉴定出几种通过自噬介导特定降解内质网(ER)成分的受体(该过程称为 ER 自噬或网质体自噬)。在这里,我们将更新关于 ER 自噬受体在健康和疾病中的作用的现有知识。

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