Prohibitin protects against oxidative stress in intestinal epithelial cells

被引:134
作者
Theiss, Arianne L.
Idell, Richard D.
Srinivasan, Shanthi
Klapproth, Jan-Michael
Jones, Dean P.
Merlin, Didier
Sitaraman, Shanthi V.
机构
[1] Emory Univ, Div Digest Dis, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Med, Div Pulm Med, Atlanta, GA 30322 USA
关键词
epithelial permeability; inflammatory bowel diseases; glutathione;
D O I
10.1096/fj.06-6801com
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
Prohibitin (PHB) is an evolutionarily conserved and ubiquitously expressed protein whose expression or function in intestinal diseases is not known. In this study, we examined the expression and role of PHB in oxidative stress associated with inflammatory bowel disease. Our results show that PHB primarily localizes to the mitochondria in intestinal epithelial cells. Its expression is down-regulated during active human Crohn's disease, experimental colitis in vivo, and oxidative stress in vitro. PHB overexpression increases the expression of glutathione-S-transferase pi and protects from oxidant-induced depletion of glutathione. Finally, PHB overexpression decreases accumulation of reactive oxygen metabolites, as well as increased permeability induced by oxidative stress in intestinal epithelial cells. Together, these results suggest that PHB constitutes a previously unrecognized cellular defense against oxidant injury. Thus, strategies to modulate PHB levels may constitute a novel therapeutic approach for intestinal inflammatory diseases, wherein oxidative stress plays a critical role in tissue injury and inflammation.
引用
收藏
页码:197 / 206
页数:10
相关论文
共 58 条
[1]  
Araki Y, 2006, INT J MOL MED, V17, P331
[2]   Evidence that nuclear factor-κB activation is critical in oxidant-induced disruption of the microtubule cytoskeleton and barrier integrity and that its inactivation is essential in epidermal growth factor-mediated protection of the monolayers of intestinal epithelia [J].
Banan, A ;
Farhadi, A ;
Fields, JZ ;
Mutlu, E ;
Zhang, L ;
Keshavarzian, A .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 306 (01) :13-28
[3]   Oxidant-induced intestinal barrier disruption and its prevention by growth factors in a human colonic cell line: Role of the microtubule cytoskeleton [J].
Banan, A ;
Choudhary, S ;
Zhang, Y ;
Fields, JZ ;
Keshavarzian, A .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (05) :727-738
[4]   Rapid development of colitis in NSAID-treated IL-10-deficient mice [J].
Berg, DJ ;
Zhang, J ;
Weinstock, JV ;
Ismail, HF ;
Earle, KA ;
Alila, H ;
Pamukcu, R ;
Moore, S ;
Lynch, RG .
GASTROENTEROLOGY, 2002, 123 (05) :1527-1542
[5]   Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin [J].
Bourges, I ;
Ramus, C ;
de Camaret, BM ;
Beugnot, R ;
Remacle, C ;
Cardol, P ;
Hofhaus, G ;
Issartel, JP .
BIOCHEMICAL JOURNAL, 2004, 383 (03) :491-499
[6]   DEPLETED MUCOSAL ANTIOXIDANT DEFENSES IN INFLAMMATORY BOWEL-DISEASE [J].
BUFFINTON, GD ;
DOE, WF .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (06) :911-918
[7]  
Campbell IG, 2003, CANCER EPIDEM BIOMAR, V12, P1273
[8]  
CARRIER JC, 2005, INT J COLORECTAL DIS, P1
[9]   Targeted deletion of metalloproteinase 9 attenuates experimental colitis in mice: Central role of epithelial-derived MMP [J].
Castaneda, FE ;
Walia, B ;
Vijay-Kumar, M ;
Patel, NR ;
Roser, S ;
Kolachala, VL ;
Rojas, M ;
Wang, LX ;
Oprea, G ;
Garg, P ;
Gewirtz, AT ;
Roman, J ;
Merlin, D ;
Sitaraman, SV .
GASTROENTEROLOGY, 2005, 129 (06) :1991-2008
[10]   Silencing a prohibitin alters plant development and senescence [J].
Chen, JC ;
Jiang, CZ ;
Reid, MS .
PLANT JOURNAL, 2005, 44 (01) :16-24