Surf4, cargo trafficking, lipid metabolism, and therapeutic implications

Author:

Shen Yishi1,Gu Hong-Mei1,Qin Shucun2,Zhang Da-Wei1ORCID

Affiliation:

1. Group on the Molecular and Cell Biology of Lipids and Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta , Edmonton, AB T6R 2G3 , Canada

2. Institute of Atherosclerosis in Shandong First Medical University (Shandong Academy of Medical Sciences) , Taian 271016 , China

Abstract

ABSTRACTSurfeit 4 is a polytopic transmembrane protein that primarily resides in the endoplasmic reticulum (ER) membrane. It is ubiquitously expressed and functions as a cargo receptor, mediating cargo transport from the ER to the Golgi apparatus via the canonical coat protein complex II (COPII)-coated vesicles or specific vesicles. It also participates in ER–Golgi protein trafficking through a tubular network. Meanwhile, it facilitates retrograde transportation of cargos from the Golgi apparatus to the ER through COPI-coated vesicles. Surf4 can selectively mediate export of diverse cargos, such as PCSK9 very low-density lipoprotein (VLDL), progranulin, α1-antitrypsin, STING, proinsulin, and erythropoietin. It has been implicated in facilitating VLDL secretion, promoting cell proliferation and migration, and increasing replication of positive-strand RNA viruses. Therefore, Surf4 plays a crucial role in various physiological and pathophysiological processes and emerges as a promising therapeutic target. However, the molecular mechanisms by which Surf4 selectively sorts diverse cargos for ER–Golgi protein trafficking remain elusive. Here, we summarize the most recent advances in Surf4, focusing on its role in lipid metabolism.

Funder

Canadian Institutes of Health Research

National Natural Science Foundation of China

Natural Sciences and Engineering Research Council of Canada

Shandong First Medical University

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Reference129 articles.

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