CRELD2, endoplasmic reticulum stress, and human diseases

被引:15
作者
Tang, Qin [1 ]
Liu, Qinhui [1 ]
Li, Yanping [1 ]
Mo, Li [2 ]
He, Jinhan [1 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Metab Dis & Pharmacotherapy, Dept Pharm, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Ctr Gerontol & Geriatr, Natl Clin Res Ctr Geriatr, Chengdu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CRELD2; endoplasmic reticulum stress; unfolded protein response; metabolism; human diseases; UNFOLDED PROTEIN RESPONSE; ATRIOVENTRICULAR SEPTAL-DEFECTS; CONGENITAL HEART-DISEASE; XBP1; MESSENGER-RNA; ER STRESS; NEUROTROPHIC FACTOR; CYSTEINE-RICH; DOWN-SYNDROME; TRANSMEMBRANE PROTEIN; DISULFIDE-ISOMERASE;
D O I
10.3389/fendo.2023.1117414
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CRELD2, a member of the cysteine-rich epidermal growth factor-like domain (CRELD) protein family, is both an endoplasmic reticulum (ER)-resident protein and a secretory factor. The expression and secretion of CRELD2 are dramatically induced by ER stress. CRELD2 is ubiquitously expressed in multiple tissues at different levels, suggesting its crucial and diverse roles in different tissues. Recent studies suggest that CRELD2 is associated with cartilage/bone metabolism homeostasis and pathological conditions involving ER stress such as chronic liver diseases, cardiovascular diseases, kidney diseases, and cancer. Herein, we first summarize ER stress and then critically review recent advances in the knowledge of the characteristics and functions of CRELD2 in various human diseases. Furthermore, we highlight challenges and present future directions to elucidate the roles of CRELD2 in human health and disease.
引用
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页数:14
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共 127 条
[1]   Endoplasmic reticulum stress in liver diseases [J].
Ajoolabady, Amir ;
Kaplowitz, Neil ;
Lebeaupin, Cynthia ;
Kroemer, Guido ;
Kaufman, Randal J. ;
Malhi, Harmeet ;
Ren, Jun .
HEPATOLOGY, 2023, 77 (02) :619-639
[2]   ER stress in obesity pathogenesis and management [J].
Ajoolabady, Amir ;
Liu, Simin ;
Klionsky, Daniel J. ;
Lip, Gregory Y. H. ;
Tuomilehto, Jaakko ;
Kavalakatt, Sina ;
Pereira, David M. ;
Samali, Afshin ;
Ren, Jun .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2022, 43 (02) :97-109
[3]   Transcriptome analysis of endothelial cell gene expression induced by growth on matrigel matrices: Identification and characterization of MAGP-2 and lumican as novel regulators of angiogenesis [J].
Albig A.R. ;
Roy T.G. ;
Becenti D.J. ;
Schiemann W.P. .
Angiogenesis, 2007, 10 (3) :197-216
[4]   Armet, a UPR-upregulated protelin, inhibits cell proliferation and ER stress-induced cell death [J].
Apostolou, Andria ;
Shen, Yuxian ;
Liang, Yan ;
Luo, Jun ;
Fang, Shengyun .
EXPERIMENTAL CELL RESEARCH, 2008, 314 (13) :2454-2467
[5]   The Sar1 GTPase coordinates biosynthetic cargo selection with endoplasmic reticulum export site assembly [J].
Aridor, M ;
Fish, KN ;
Bannykh, S ;
Weissman, J ;
Roberts, TH ;
Lippincott-Schwartz, J ;
Balch, WE .
JOURNAL OF CELL BIOLOGY, 2001, 152 (01) :213-229
[6]   Src regulates Golgi structure and KDEL receptor-dependent retrograde transport to the endoplasmic reticulum [J].
Bard, F ;
Mazelin, L ;
Péchoux-Longin, C ;
Malhotra, V ;
Jurdic, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (47) :46601-46606
[7]   Creld1 regulates myocardial development and function [J].
Beckert, Vera ;
Rassmann, Sebastian ;
Kayvanjoo, Amir Hossein ;
Klausen, Christina ;
Bonaguro, Lorenzo ;
Botermann, Dominik Simon ;
Krause, Melanie ;
Moreth, Kristin ;
Spielmann, Nadine ;
da Silva-Buttkus, Patricia ;
Fuchs, Helmut ;
Gailus-Durner, Valerie ;
de Angelis, Martin Hrabe ;
Haendler, Kristian ;
Ulas, Thomas ;
Aschenbrenner, Anna C. ;
Mass, Elvira ;
Wachten, Dagmar .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2021, 156 :45-56
[8]   ATF6α induces XBP1-independent expansion of the endoplasmic reticulum [J].
Bommiasamy, Hemamalini ;
Back, Sung Hoon ;
Fagone, Paolo ;
Lee, Kyungho ;
Meshinchi, Sasha ;
Vink, Elizabeth ;
Sriburi, Rungtawan ;
Frank, Matthew ;
Jackowski, Suzanne ;
Kaufman, Randal J. ;
Brewer, Joseph W. .
JOURNAL OF CELL SCIENCE, 2009, 122 (10) :1626-1636
[9]   CRELD1 modulates homeostasis of the immune system in mice and humans [J].
Bonaguro, Lorenzo ;
Koehne, Maren ;
Schmidleithner, Lisa ;
Schulte-Schrepping, Jonas ;
Warnat-Herresthal, Stefanie ;
Horne, Arik ;
Kern, Paul ;
Guenther, Patrick ;
ter Horst, Rob ;
Jaeger, Martin ;
Rahmouni, Souad ;
Georges, Michel ;
Falk, Christine S. ;
Li, Yang ;
Mass, Elvira ;
Beyer, Marc ;
Joosten, Leo A. B. ;
Netea, Mihai G. ;
Ulas, Thomas ;
Schultze, Joachim L. ;
Aschenbrenner, Anna C. .
NATURE IMMUNOLOGY, 2020, 21 (12) :1517-+
[10]   ROCK-mediated selective activation of PERK signalling causes fibroblast reprogramming and tumour progression through a CRELD2-dependent mechanism [J].
Boyle, Sarah Theresa ;
Poltavets, Valentina ;
Kular, Jasreen ;
Pyne, Natasha Theresa ;
Sandow, Jarrod John ;
Lewis, Alexander Charles ;
Murphy, Kendelle Joan ;
Kolesnikoff, Natasha ;
Moretti, Paul Andre Bartholomew ;
Tea, Melinda Nay ;
Tergaonkar, Vinay ;
Timpson, Paul ;
Pitson, Stuart Maxwell ;
Webb, Andrew Ian ;
Whitfield, Robert John ;
Lopez, Angel Francisco ;
Kochetkova, Marina ;
Samuel, Michael Susithiran .
NATURE CELL BIOLOGY, 2020, 22 (07) :882-+