Hypoxia induces apoptosis in SV40-immortalized rat proximal tubular cells through the mitochondrial pathways, devoid of HIFI-mediated upregulation of Bax

被引:66
作者
Tanaka, T
Hanafusa, N
Ingelfinger, JR
Ohse, T
Fujita, T
Nangaku, M
机构
[1] Univ Tokyo, Sch Med, Div Nephrol & Endocrinol, Bunkyo Ku, Tokyo 113, Japan
[2] Massachusetts Gen Hosp, Div Pediat Nephrol, Boston, MA 02114 USA
关键词
IRPTC; bcl2; caspase-9; p53;
D O I
10.1016/S0006-291X(03)01557-2
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
Chronic hypoxia is a major contributor to tubulointerstitial injury in various renal diseases and apoptosis is apparently involved. Although many studies report hypoxia-induced apoptosis in cultured tubular cells, information has been limited in proximal tubular cells, those from the most susceptible portion of renal tubules against hypoxia. This study was to confirm a role for apoptosis in hypoxic proximal tubular cells and to investigate its association with HIF-1. Temperature-sensitive SV40-immortalized rat proximal tubular cells (IRPTCs) showed apoptosis in 21.9+/-2.9% by hypoxia (0.2% O-2, 48 h), with alterations in mitochondrial signaling such as Bcl2 and caspase-9. Bax mRNA was unaffected during the process. However, treating IRPTCs at the nonpermissive temperature showed an upregulation of Bax by hypoxia, which was abrogated by overexpressing dominant-negative HIF-1alpha. These findings extend previous reports on hypoxia-mediated tubular cell apoptosis and demonstrate the possible involvement of HIF-1 as an upstream molecule of Bax. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:222 / 231
页数:10
相关论文
共 41 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   THE PATHOGENESIS OF CHRONIC RENAL-FAILURE [J].
BOHLE, A ;
KRESSEL, G ;
MULLER, CA ;
MULLER, GA .
PATHOLOGY RESEARCH AND PRACTICE, 1989, 185 (04) :421-440
[3]   DISPARATE MECHANISMS FOR HYPOXIC CELL INJURY IN DIFFERENT NEPHRON SEGMENTS - STUDIES IN THE ISOLATED PERFUSED RAT-KIDNEY [J].
BREZIS, M ;
SHANLEY, P ;
SILVA, P ;
SPOKES, K ;
LEAR, S ;
EPSTEIN, FH ;
ROSEN, S .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (05) :1796-1806
[4]  
CHOU JY, 1985, METHOD ENZYMOL, V109, P385
[5]  
ELDEIRY WS, 1994, CANCER RES, V54, P1169
[6]   Partial ATP depletion induces Fas- and caspase-mediated apoptosis in MDCK cells [J].
Feldenberg, LR ;
Thevananther, S ;
Del Rio, M ;
De Leon, M ;
Devarajan, P .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 276 (06) :F837-F846
[7]   Is there a common mechanism for the progression of different types of renal diseases other than proteinuria? Towards the unifying theme of chronic hypoxia [J].
Fine, LG ;
Bandyopadhyay, D ;
Norman, JT .
KIDNEY INTERNATIONAL, 2000, 57 :S22-S26
[8]   HYPOXIA INDUCES ACCUMULATION OF P53 PROTEIN, BUT ACTIVATION OF A G(1)-PHASE CHECKPOINT BY LOW-OXYGEN CONDITIONS IS INDEPENDENT OF P53 STATUS [J].
GRAEBER, TG ;
PETERSON, JF ;
TSAI, M ;
MONICA, K ;
FORNACE, AJ ;
GIACCIA, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :6264-6277
[9]   Enforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosis [J].
Gross, A ;
Jockel, J ;
Wei, MC ;
Korsmeyer, SJ .
EMBO JOURNAL, 1998, 17 (14) :3878-3885
[10]   Hypoxia-inducible factor-1α mediates hypoxia-induced delayed neuronal death that involves p53 [J].
Halterman, MW ;
Miller, CC ;
Federoff, HJ .
JOURNAL OF NEUROSCIENCE, 1999, 19 (16) :6818-6824