ORP150 protects against hypoxia/ischemia-induced neuronal death

被引:171
作者
Tamatani, M [1 ]
Matsuyama, T
Yamaguchi, A
Mitsuda, N
Tsukamoto, Y
Taniguchi, M
Che, YH
Ozawa, K
Hori, O
Nishimura, H
Yamashita, A
Okabe, M
Yanagi, H
Stern, DM
Ogawa, S
Tohyama, M
机构
[1] Osaka Univ, Grad Sch Med, Dept Anat & Neurosci, Osaka, Japan
[2] Hyogo Coll Med, Dept Internal Med 5, Hyogo, Japan
[3] Natl Ctr Cardiac Dis & Circulat Res, Dept Pathol, Osaka, Japan
[4] Kanazawa Univ, Sch Med, Dept Neuroanat, Kanazawa, Ishikawa 920, Japan
[5] HSP Res Inst, Kyoto, Japan
[6] Osaka Univ, Genome Informat Res Ctr, Osaka, Japan
[7] Columbia Univ, Coll Phys & Surg, CREST, JST, New York, NY USA
[8] Columbia Univ, Coll Phys & Surg, Dept Physiol & Cellular Biophys, New York, NY USA
关键词
D O I
10.1038/85463
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
Oxygen-regulated protein 150 kD (ORP150) is a novel endoplasmic-reticulum-associated chaperone induced by hypoxia/ischemia. Although ORP150 was sparingly upregulated in neurons from human brain undergoing ischemic stress, there was robust induction in astrocytes. Cultured neurons overexpressing ORP150 were resistant to hypoxemic stress, whereas astrocytes with inhibited ORP150 expression were more vulnerable. Mice with targeted neuronal overexpression of ORP150 had smaller strokes compared with controls. Neurons with increased ORP150 demonstrated suppressed caspase-3-like activity and enhanced brain-derived neurotrophic factor (BDNF) under hypoxia signaling. These data indicate that ORP150 is an integral participant in ischemic cytoprotective pathways.
引用
收藏
页码:317 / 323
页数:7
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