Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/128211
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Type: Journal article
Title: Cell surface expression of 78-kDa glucose-regulated protein (GRP78) mediates diabetic nephropathy
Author: Van Krieken, R.
Mehta, N.
Wang, T.
Zheng, M.
Li, R.
Gao, B.
Ayaub, E.
Ask, K.
Paton, J.C.
Paton, A.W.
Austin, R.C.
Krepinsky, J.C.
Citation: Journal of Biological Chemistry, 2019; 294(19):7755-7768
Publisher: American Society for Biochemistry and Molecular Biology
Issue Date: 2019
ISSN: 0021-9258
1083-351X
Statement of
Responsibility: 
Richard Van Krieken, Neel Mehta, Tony Wang, Mengyu Zheng, Renzhong Li, Bo Gao, Ehab Ayaub, Kjetil Ask, James C. Paton, Adrienne W. Paton, X Richard C. Austin, and X Joan C. Krepinsky
Abstract: The 78-kDa glucose-regulated protein (GRP78) is a well-established endoplasmic reticulum (ER)-resident chaperone that maintains protein homeostasis and regulates the unfolded protein response. Under conditions of ER stress, GRP78 is also expressed at the cell surface and implicated in tumorigenesis, immunity, and cellular signaling events. The role of cell surface-associated GRP78 (csGRP78) in the pathogenesis of diabetic nephropathy has not yet been defined. Here we explored the role of csGRP78 in regulating high glucose (HG)-induced profibrotic AKT Ser/Thr kinase (AKT) signaling and up-regulation of extracellular matrix proteins. Using primary kidney mesangial cells, we show that HG treatment, but not the osmotic control mannitol, induces csGRP78 expression through an ER stress-dependent mechanism. We found that csGRP78, known to be located on the outer membrane leaflet, interacts with the transmembrane protein integrin β1 and activates focal adhesion kinase and downstream PI3K/AKT signaling. Localization of GRP78 at the cell surface and its interaction with integrin β1 were also required for extracellular matrix protein synthesis in response to HG. Surprisingly, both the N and C termini of csGRP78 were necessary for this profibrotic response. Increased localization of GRP78 at the plasma membrane was also found in the glomerular mesangial area of type 1 diabetic mice in two different models (streptozotocin-induced and Akita). In freshly isolated glomeruli from Akita mice, csGRP78 co-localized with the mesangial cell surface marker α8-integrin. In conclusion, our work reveals a role for csGRP78 in HG-induced profibrotic responses in mesangial cells, informing a potential approach to treating diabetic nephropathy.
Keywords: 78-kDa glucose-regulated protein (GRP78)
Description: Published, Papers in Press, March 26, 2019.
Rights: © 2019 Van Krieken et al. Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.
RMID: 0030112734
DOI: 10.1074/jbc.RA118.006939
Appears in Collections:Molecular and Biomedical Science publications

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