共 80 条
cDNA microarray analysis of changes in gene expression induced by neuronal hypoxia in vitro
被引:65
作者:

Jin, K
论文数: 0 引用数: 0
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机构: Buck Inst Age Res, Novato, CA 94945 USA

Mao, XO
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h-index: 0
机构: Buck Inst Age Res, Novato, CA 94945 USA

Eshoo, MW
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机构: Buck Inst Age Res, Novato, CA 94945 USA

del Rio, G
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机构: Buck Inst Age Res, Novato, CA 94945 USA

Rao, R
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机构: Buck Inst Age Res, Novato, CA 94945 USA

Chen, D
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h-index: 0
机构: Buck Inst Age Res, Novato, CA 94945 USA

Simon, RP
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机构: Buck Inst Age Res, Novato, CA 94945 USA

Greenberg, DA
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h-index: 0
机构: Buck Inst Age Res, Novato, CA 94945 USA
机构:
[1] Buck Inst Age Res, Novato, CA 94945 USA
[2] Legacy Res, Robert S Dow Neurobiol Lab, Portland, OR 97208 USA
关键词:
microarray;
hypoxia;
endoplasmic reticulum;
ubiquitination;
hypoxia-inducible factor-1;
D O I:
10.1023/A:1020913123054
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:
We used cDNA microarray gene expression profiling to characterize the transcriptional response to exposure of cultured mouse cerebral cortical neurons to hypoxia for 24 hr. Of 11,200 genes examined, 1,405 (12.5%) were induced or repressed at least 1.5-fold, whereas 26 known genes were induced and 20 known genes were repressed at least 2.5-fold. The most strongly induced genes included genes coding for endoplasmic reticulum proteins (Ero1L/Giig11, Sac1p, Ddit3/Gadd153), proteins involved in ubiquitination (Arih2, P4hb), proteins induced by hypoxia in non-neuronal systems (Gpi1, Aldo1, Anxa2, Hig1), and proteins that might promote cell death (Gas5, Egr1, Ndr1, Vdac2). These findings reinforce the importance of endoplasmic reticulum-based mechanisms and of protein-ubiquitination pathways in the neuronal response to hypoxia.
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页码:1105 / 1112
页数:8
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