Mutation of the trkB gene encoding the high-affinity receptor for brain-derived neurotrophic factor in stroke-prone spontaneously hypertensive rats

被引:14
作者
Kageyama, H
Nemoto, K
Nemoto, F
Sekimoto, M
Nara, Y
Nabika, T
Iwayama, Y
Fukamachi, K
Tomita, I
Senba, E
Forehand, CJ
Hendley, ED
Ueyama, T
机构
[1] UNIV SHIZUOKA, SCH PHARMACEUT SCI, LAB HLTH SCI, SHIZUOKA 422, JAPAN
[2] KYOTO UNIV, GRAD SCH HUMAN & ENVIRONM STUDIES, KYOTO, JAPAN
[3] SHIMANE MED UNIV, DEPT LAB MED, IZUMO, SHIMANE, JAPAN
[4] WAKAYAMA MED COLL, DEPT ANAT & NEUROBIOL, WAKAYAMA 640, JAPAN
[5] UNIV VERMONT, DEPT ANAT & NEUROBIOL, BURLINGTON, VT 05405 USA
[6] UNIV VERMONT, DEPT MOL PHYSIOL & BIOPHYS, BURLINGTON, VT 05405 USA
关键词
D O I
10.1006/bbrc.1996.1870
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
Brain-derived neurotrophic factor and its receptor, trkB, are thought to play a crucial role for protection against neuronal death induced by brain ischemia, such as in stroke. In the present study we found a missense mutation in the trkB gene from all of the five substrains of stroke-prone spontaneously hypertensive rats (SHRSP) that were examined. This mutation was not found in six out of seven hypertensive but stroke-resistant ancestral strains (SHR) of SHRSP. nor in any of seven strains of normotensive, non-stroke-prone strains. Hippocampal neurons, which are particularly vulnerable to damage in stroke, were shown to be more susceptible to ischemic damage in SHRSP than in either SHR or normotensive stroke-resistant controls. The association of a mutated trkB gene with the stroke-prone genotype found in this study suggests that the trkB gene merits further study as a promising candidate gene for stroke. (C) 1996 Academic Press
引用
收藏
页码:713 / 718
页数:6
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