Haem oxygenase-1 prevents cell death by regulating cellular iron

被引:461
作者
Ferris, CD [1 ]
Jaffrey, SR
Sawa, A
Takahashi, M
Brady, SD
Barrow, RK
Tysoe, SA
Wolosker, H
Barañano, DE
Doré, S
Poss, KD
Snyder, SH
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Div Gastroenterol, Baltimore, MD 21205 USA
[3] Skidmore Coll, Dept Chem & Phys, Saratoga Springs, NY 12866 USA
[4] MIT, Dept Biol, Cambridge, MA 02139 USA
[5] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
关键词
D O I
10.1038/11072
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Haem oxygenase-1 (HO1) is a heat-shock protein that is induced by stressful stimuli. Here we demonstrate a cytoprotective role for HO1: cell death produced by serum deprivation, staurosporine or etoposide is markedly accentuated in cells from mice with a targeted deletion of the HO1 gene, and greatly reduced in cells that overexpress HO1. Iron efflux from cells is augmented by HO1 transfection and reduced in HO1-deficient fibroblasts, Iron accumulation in HO1-deficient cells explains their death: iron chelators protect HO1-deficient fibroblasts from cell death. Thus, cytoprotection by HO1 is attributable to its augmentation of iron efflux, reflecting a role for HO1 in modulating intracellular iron levels and regulating cell viability.
引用
收藏
页码:152 / 157
页数:6
相关论文
共 39 条
[1]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[2]  
Baranano DE, 1999, GASTROENTEROLOGY, V116, pA1188
[3]  
BOTHWELL TH, 1995, METABOLIC MOL BASES, P2237
[4]  
BREDT DS, 1992, J BIOL CHEM, V267, P10976
[5]   The Hsp70 and Hsp60 chaperone machines [J].
Bukau, B ;
Horwich, AL .
CELL, 1998, 92 (03) :351-366
[6]   INDUCTION OF HEME OXYGENASE-1 GENE-EXPRESSION BY LIPOPOLYSACCHARIDE IS MEDIATED BY AP-1 ACTIVATION [J].
CAMHI, SL ;
ALAM, J ;
OTTERBEIN, L ;
SYLVESTER, SL ;
CHOI, AMK .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 13 (04) :387-398
[7]   Heme oxygenase-1: Function, regulation, and implication of a novel stress-inducible protein in oxidant-induced lung injury [J].
Choi, AMK ;
Alam, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 15 (01) :9-19
[8]  
Conrad ME, 1998, SEMIN HEMATOL, V35, P1
[9]   Oxygen toxicity and iron accumulation in the lungs of mice lacking heme oxygenase-2 [J].
Dennery, PA ;
Spitz, DR ;
Yang, G ;
Tatarov, A ;
Lee, CS ;
Shegog, ML ;
Poss, KD .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :1001-1011
[10]   REGULATION OF FERRITIN AND HEME OXYGENASE SYNTHESIS IN RAT FIBROBLASTS BY DIFFERENT FORMS OF IRON [J].
EISENSTEIN, RS ;
GARCIAMAYOL, D ;
PETTINGELL, W ;
MUNRO, HN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :688-692