GRP78 at the Centre of the Stage in Cancer and Neuroprotection

被引:194
作者
Casas, Caty [1 ]
机构
[1] Univ Autonoma Barcelona, Inst Neurociencies, Dept Cell Biol Physiol & Immunol, Barcelona, Spain
关键词
GRP78; BiP; neuroprotection; endogenous mechanisms; neurodegeneration; ER stress; autophagy; ERAD; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED-PROTEIN-RESPONSE; GLUCOSE-REGULATED PROTEIN; CELL-SURFACE GRP78; AMYLOID PRECURSOR PROTEIN; CHAIN-BINDING-PROTEIN; COOH-TERMINAL DOMAIN; RIBOSOME ENTRY SITE; BIP MESSENGER-RNA; NF-KAPPA-B;
D O I
10.3389/fnins.2017.00177
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The 78-kDa glucose-regulated protein GRP78, also known as BiP and HSP5a, is a multifunctional protein with activities far beyond its well-known role in the unfolded protein response (UPR) which is activated after endoplasmic reticulum (ER) stress in the cells. Most of these newly discovered activities depend on its position within the cell. GRP78 is located mainly in the ER, but it has also been observed in the cytoplasm, the mitochondria, the nucleus, the plasma membrane, and secreted, although it is dedicated mostly to engage endogenous cytoprotective processes. Hence, GRP78 may control either UPR and macroautophagy or may activated phosphatidylinositol 3-kinase (PI3K)/AKT pro-survival pathways. GRP78 influences how tumor cells survive, proliferate, and develop chemoresistance. In neurodegeneration, endogenous mechanisms of neuroprotection are frequently insufficient or dysregulated. Lessons from tumor biology may give us clues about how boosting endogenous neuroprotective mechanisms in age-related neurodegeneration. Herein, the functions of GRP78 are revealed at the center of the stage of apparently opposite sites of the same coin regarding cytoprotection: neurodegeneration and cancer. The goal is to give a comprehensive and critical review that may serve to guide future experiments to identify interventions that will enhance neuroprotection.
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页数:15
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共 168 条
[1]   Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation [J].
Abou Ezzi, Samer ;
Urushitani, Makoto ;
Julien, Jean-Pierre .
JOURNAL OF NEUROCHEMISTRY, 2007, 102 (01) :170-178
[2]   The molecular mechanisms underlying BiP-mediated gating of the Sec61 translocon of the endoplasmic reticulum [J].
Alder, NN ;
Shen, Y ;
Brodsky, JL ;
Hendershot, LM ;
Johnson, AE .
JOURNAL OF CELL BIOLOGY, 2005, 168 (03) :389-399
[3]   A BINDING-SITE FOR THE CYCLIC ADENOSINE 3',5'-MONOPHOSPHATE-RESPONSE ELEMENT-BINDING PROTEIN AS A REGULATORY ELEMENT IN THE GRP78-PROMOTER [J].
ALEXANDRE, S ;
NAKAKI, T ;
VANHAMME, L ;
LEE, AS .
MOLECULAR ENDOCRINOLOGY, 1991, 5 (12) :1862-1872
[4]   Mitochondria-associated ER membranes and Alzheimer disease [J].
Area-Gomez, Estela ;
Schon, Eric A. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2016, 38 :90-96
[5]   Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum [J].
Axe, Elizabeth L. ;
Walker, Simon A. ;
Manifava, Maria ;
Chandra, Priya ;
Roderick, H. Llewelyn ;
Habermann, Anja ;
Griffiths, Gareth ;
Ktistakis, Nicholas T. .
JOURNAL OF CELL BIOLOGY, 2008, 182 (04) :685-701
[6]   Tyrosine gated electron transfer is key to the toxic mechanism of Alzheimer's disease β-amyloid [J].
Barnham, KJ ;
Haeffner, F ;
Ciccotosto, GD ;
Curtain, CC ;
Tew, D ;
Mavros, C ;
Beyreuther, K ;
Carrington, D ;
Masters, CL ;
Cherny, RA ;
Cappai, R ;
Bush, AI .
FASEB JOURNAL, 2004, 18 (10) :1427-+
[7]   Induction of the unfolded protein response by α-synuclein in experimental models of Parkinson's disease [J].
Bellucci, Arianna ;
Navarria, Laura ;
Zaltieri, Michela ;
Falarti, Elisa ;
Bodei, Serena ;
Sigala, Sandra ;
Battistin, Leontino ;
Spillantini, MariaGrazia ;
Missale, Cristina ;
Spano, PierFranco .
JOURNAL OF NEUROCHEMISTRY, 2011, 116 (04) :588-605
[8]   Dynamic interaction of BiP and ER stress transducers in the unfolded-protein response [J].
Bertolotti, A ;
Zhang, YH ;
Hendershot, LM ;
Harding, HP ;
Ron, D .
NATURE CELL BIOLOGY, 2000, 2 (06) :326-332
[9]   GRP78 is a novel receptor initiating a vascular barrier protective response to oxidized phospholipids [J].
Birukova, Anna A. ;
Singleton, Patrick A. ;
Gawlak, Grzegorz ;
Tian, Xinyong ;
Mirzapoiazova, Tamara ;
Mambetsariev, Bolot ;
Dubrovskyi, Oleksii ;
Oskolkova, Olga V. ;
Bochkov, Valery N. ;
Birukov, Konstantin G. .
MOLECULAR BIOLOGY OF THE CELL, 2014, 25 (13) :2006-2016
[10]   AFFINITY PANNING OF A LIBRARY OF PEPTIDES DISPLAYED ON BACTERIOPHAGES REVEALS THE BINDING-SPECIFICITY OF BIP [J].
BLONDELGUINDI, S ;
CWIRLA, SE ;
DOWER, WJ ;
LIPSHUTZ, RJ ;
SPRANG, SR ;
SAMBROOK, JF ;
GETHING, MJH .
CELL, 1993, 75 (04) :717-728