Coordination of inter-organelle communication and lipid fluxes by OSBP-related proteins

被引:39
作者
Arora, Amita
Taskinen, Juuso H.
Olkkonen, Vesa M. [1 ]
机构
[1] Univ Helsinki, Fac Med, Minerva Fdn Inst Med Res, Helsinki, Finland
基金
芬兰科学院;
关键词
Cell signalling; Lipid metabolism; Lipid transport; Membrane contact site; ORP; OSBPL; OXYSTEROL-BINDING-PROTEIN; HAMSTER OVARY CELLS; MEMBRANE CONTACT SITES; LEUCINE ZIPPER PROTEIN; NUCLEAR RECEPTOR LXR; PLASMA-MEMBRANE; ENDOPLASMIC-RETICULUM; GENE-EXPRESSION; CHOLESTEROL TRANSPORT; R-RAS;
D O I
10.1016/j.plipres.2022.101146
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxysterol-binding protein (OSBP) and OSBP-related proteins (ORPs) constitute one of the largest families of lipid-binding/transfer proteins (LTPs) in eukaryotes. The current view is that many of them mediate interorganelle lipid transfer over membrane contact sites (MCS). The transfer occurs in several cases in a 'countercurrent' fashion: A lipid such as cholesterol or phosphatidylserine (PS) is transferred against its concentration gradient driven by transport of a phosphoinositide in the opposite direction. In this way ORPs are envisioned to maintain the distinct organelle lipid compositions, with impacts on multiple organelle functions. However, the functions of ORPs extend beyond lipid homeostasis to regulation of processes such as cell survival, proliferation and migration. Important expanding areas of mammalian ORP research include their roles in viral and bacterial infections, cancers, and neuronal function. The yeast OSBP homologue (Osh) proteins execute multifaceted functions in sterol and glycerophospholipid homeostasis, post-Golgi vesicle transport, phosphatidylinositol-4-phosphate, sphingolipid and target of rapamycin (TOR) signalling, and cell cycle control. These observations identify ORPs as lipid transporters and coordinators of signals with an unforeseen variety of cellular processes. Understanding their activities not only enlightens the biology of the living cell but also allows their employment as targets of new therapeutic approaches for disease.
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页数:22
相关论文
共 286 条
[21]   RAT-LIVER CYTOSOL OXYSTEROL-BINDING PROTEIN - CHARACTERIZATION AND COMPARISON WITH THE HTC CELL PROTEIN [J].
BESEME, F ;
ASTRUC, ME ;
DEFAY, R ;
DEPAULET, AC .
FEBS LETTERS, 1987, 210 (01) :97-103
[22]   CHARACTERIZATION OF OXYSTEROL-BINDING PROTEIN IN RAT EMBRYO FIBROBLASTS AND VARIATIONS AS A FUNCTION OF THE CELL-CYCLE [J].
BESEME, F ;
ASTRUC, ME ;
DEFAY, R ;
DESCOMPS, B ;
DEPAULET, AC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 886 (01) :96-108
[23]   Phosphoinositides in the Hepatitis C Virus Life Cycle [J].
Bishe, Bryan ;
Syed, Gulam ;
Siddiqui, Aleem .
VIRUSES-BASEL, 2012, 4 (10) :2340-2358
[24]   Association of OSBPL11 Gene Polymorphisms With Cardiovascular Disease Risk Factors in Obesity [J].
Bouchard, Luigi ;
Faucher, Genevieve ;
Tchernof, Andre ;
Deshaies, Yves ;
Marceau, Simon ;
Lescelleur, Odette ;
Biron, Simon ;
Bouchard, Claude ;
Perusse, Louis ;
Vohl, Marie-Claude .
OBESITY, 2009, 17 (07) :1466-1472
[25]   ORP1L mediated PI(4)P signaling at ER-lysosome-mitochondrion three-way contact contributes to mitochondrial division [J].
Boutry, Maxime ;
Kim, Peter K. .
NATURE COMMUNICATIONS, 2021, 12 (01)
[26]   Retrospective on Cholesterol Homeostasis: The Central Role of Scap [J].
Brown, Michael S. ;
Radhakrishnan, Arun ;
Goldstein, Joseph L. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87, 2018, 87 :783-807
[27]   Natural products reveal cancer cell dependence on oxysterol-binding proteins [J].
Burgett, Anthony W. G. ;
Poulsen, Thomas B. ;
Wangkanont, Kittikhun ;
Anderson, D. Ryan ;
Kikuchi, Chikako ;
Shimada, Kousei ;
Okubo, Shuichi ;
Fortner, Kevin C. ;
Mimaki, Yoshihiro ;
Kuroda, Minpei ;
Murphy, Jason P. ;
Schwalb, David J. ;
Petrella, Eugene C. ;
Cornella-Taracido, Ivan ;
Schirle, Markus ;
Tallarico, John A. ;
Shair, Matthew D. .
NATURE CHEMICAL BIOLOGY, 2011, 7 (09) :639-647
[28]   The phosphoinositide 3-kinase pathway [J].
Cantley, LC .
SCIENCE, 2002, 296 (5573) :1655-1657
[29]  
Cao X, 2019, FASEB J, V12, P33
[30]   Adenovirus Reveals New Pathway for Cholesterol Egress from the Endolysosomal System [J].
Carlin, Cathleen ;
Manor, Danny .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (16) :1-16