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Am J Physiol Cell Physiol 294: C641-C650, 2008. First published December 19, 2007; doi:10.1152/ajpcell.00400.2007
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PROTEIN AND VESICLE TRAFFICKING, CYTOSKELETON

Targeting of the molecular chaperone oxygen-regulated protein 150 (ORP150) to mitochondria and its induction by cellular stress

David D. Arrington and Rick G. Schnellmann

Department of Pharmaceutical Sciences, Medical University of South Carolina, Charleston, South Carolina

Submitted 4 September 2007 ; accepted in final form 14 December 2007

Oxygen-regulated protein 150 (ORP150) is an inducible endoplasmic reticulum (ER) chaperone molecule that is upregulated after numerous cellular insults and has a cytoprotective role in renal, neural, and cardiac models of ischemia-reperfusion injury. ORP150 also has been shown to play a role in cellular Ca2+ homeostasis, and in turn, regulating calpain activity. In this study, we identified ORP150 in whole rat renal cortical mitochondria and matrix fractions, demonstrated the targeting of an ORP150-GFP construct to the mitochondria of NIH-3T3 cells, and showed that the NH2-terminal 13 amino acids of ORP150 are sufficient for this translocation. ORP150 expression was found to be regulated by the anti-C/enhancer-binding protein homologous protein (CHOP)/GADD153 transcription factor and ORP150 levels increased in the mitochondria and ER of COS-7 cells after diverse stresses, including hypoxia, serum starvation, prolyl hydroxylase inhibition with dimethyloxaloylglycine, and exposure to tunicamycin, ethidium, bromide, and 2-deoxyglucose. Induction of the mitochondrial specific stress response in COS-7 cells through expression of an ornithine transcarbamylase mutant ({Delta}OTC) increased mitochondrial ORP150 levels and mitochondrial calpain activity. To determine whether mitochondrial ORP150 and mitochondrial calpain 10 interact, rat cortical mitochondria exposed to Ca2+ resulted in ORP150 cleavage in a calpain inhibitor-dependent manner, revealing that ORP150 is a substrate and may be regulated by calpain 10. These data reveal a novel cellular localization for ORP150 and that mitochondrial ORP150 is upregulated by CHOP/GADD153 in response to mitochondrial and ER stress. Our data also reveal that ORP150 is a substrate for mitochondrial calpain 10.

calpain; endoplasmic reticulum



Address for reprint requests and other correspondence: R. G. Schnellmann, Dept. of Pharmaceutical Sciences, Medical Univ. of South Carolina, 280 Calhoun St., Charleston, SC 29425 (e-mail: schnell{at}musc.edu)




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Am. J. Physiol. Renal Physiol.Home page
M. D. Covington, D. D. Arrington, and R. G. Schnellmann
Calpain 10 is required for cell viability and is decreased in the aging kidney
Am J Physiol Renal Physiol, March 1, 2009; 296(3): F478 - F486.
[Abstract] [Full Text] [PDF]




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