HIF-1α reveals a binding activity to the promoter of iNOS gene after permanent middle cerebral artery occlusion

被引:69
作者
Matrone, C
Pignataro, G
Molinaro, P
Irace, C
Scorziello, A
Di Renzo, GF
Annunziato, L
机构
[1] Univ Naples Federico II, Dept Neurosci, Div Pharmacol, I-80131 Naples, Italy
[2] Univ Naples Federico II, Sch Pharm, Dept Expt Pharmacol, Naples, Italy
关键词
hippocampus; hypoxia inducible factor-1; inducible nitric oxide synthase; inducible nitric oxide synthase promoter; ischemia; pMCAO;
D O I
10.1111/j.1471-4159.2004.02483.x
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
Hypoxia inducible factor (HIF-1)-1alpha is a specific, oxygen-sensitive protein that regulates the activity of HIF-1, a transcriptional factor that increases after cerebral ischemia and may either promote or prevent neuronal survival. In this study to determine whether the inducible nitric oxide synthase (iNOS) gene containing the sequence of the hypoxia-responsive enhancer (HRE) was an HIF-1 target after cerebral ischemia induced by permanent middle cerebral artery occlusion (pMCAO), electrophoretic mobility shift assay (EMSA) and iNOS western blot analysis were performed in the ischemic core, in the area surrounding the infarct and in the hippocampus ipsilateral and contralateral to the lesion. In addition, both HIF-1alpha mRNA and protein expression were examined in the ischemic core, in the area surrounding the ischemic core and in the hippocampus ipsilateral to the insult. Our results revealed that pMCAO up-regulates iNOS protein in the ischemic core, in the area surrounding the ischemic core and in the hippocampus ipsilateral to the lesion, and that the activation of iNOS expression is mediated by HIF-1. Moreover, HIF-1alpha mRNA and protein levels increased in the ischemic core and in the hippocampus ipsilateral to the lesion compared with the levels obtained in the corresponding areas of sham-operated controls or in the contralateral hemisphere. Particularly in the area surrounding the ischemic core, HIF-1alpha protein accumulated during pMCAO although mRNA did not increase. Our study suggests that the activation of HIF-1 might be involved in the mechanisms whereby iNOS promotes cell survival and/or death after cerebral ischemia.
引用
收藏
页码:368 / 378
页数:11
相关论文
共 43 条
[1]   Induction of hypoxia-inducible factor-1 (HIF-1) and its target genes following focal ischaemia in rat brain [J].
Bergeron, M ;
Yu, AY ;
Solway, KE ;
Semenza, GL ;
Sharp, FR .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (12) :4159-4170
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Neurodegeneration in the rat hippocampus and striatum after middle cerebral artery occlusion [J].
Butler, TL ;
Kassed, CA ;
Sanberg, PR ;
Willing, AE ;
Pennypacker, KR .
BRAIN RESEARCH, 2002, 929 (02) :252-260
[4]  
Chavez JC, 2002, J NEUROSCI, V22, P8922
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   Use of brain slices in the study of pathogenic role of inducible nitric oxide synthase in cerebral ischemia-reperfusion [J].
De Alba, J ;
Cárdenas, A ;
Moro, MA ;
Leza, JC ;
Lorenzo, P ;
Lizasoain, I .
GENERAL PHARMACOLOGY, 1999, 32 (05) :577-581
[7]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[8]  
GOLBERG MP, 1990, STROKE, V21, P75
[9]   NITRIC-OXIDE - PATHOPHYSIOLOGICAL MECHANISMS [J].
GROSS, SS ;
WOLIN, MS .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :737-769
[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