Autophagy of the ER: the secretome finds the lysosome

Author:

Knupp Jeffrey12,Pletan Madison L.12,Arvan Peter3,Tsai Billy12ORCID

Affiliation:

1. Department of Cell and Developmental Biology University of Michigan Medical School Ann Arbor MI USA

2. Cellular and Molecular Biology Program University of Michigan Medical School Ann Arbor MI USA

3. Division of Metabolism, Endocrinology & Diabetes, Department of Internal Medicine University of Michigan Medical School Ann Arbor MI USA

Abstract

Lysosomal degradation of the endoplasmic reticulum (ER) and its components through the autophagy pathway has emerged as a major regulator of ER proteostasis. Commonly referred to as ER‐phagy and ER‐to‐lysosome‐associated degradation (ERLAD), how the ER is targeted to the lysosome has been recently clarified by a growing number of studies. Here, we summarize the discoveries of the molecular components required for lysosomal degradation of the ER and their proposed mechanisms of action. Additionally, we discuss how cells employ these machineries to create the different routes of ER‐lysosome‐associated degradation. Further, we review the role of ER‐phagy in viral infection pathways, as well as the implication of ER‐phagy in human disease. In sum, we provide a comprehensive overview of the current field of ER‐phagy.

Funder

Division of Diabetes, Endocrinology, and Metabolic Diseases

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

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