Mechanisms of neuroprotection by a novel rescue factor humanin from Swedish mutant amyloid precursor protein

被引:197
作者
Hashimoto, Y
Ito, Y
Niikura, T
Shao, Z
Hata, M
Oyama, F
Nishimoto, I
机构
[1] Keio Univ, Sch Med, Dept Pharmacol & Neurosci, Shinjuku Ku, Tokyo 1608582, Japan
[2] Univ Tokyo, Sch Med, Dept Neuropathol, Bunkyo Ku, Tokyo 1130033, Japan
关键词
D O I
10.1006/bbrc.2001.4765
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 report a novel gene, designated Humanin (HN) cDNA, that suppresses neuronal cell death by K595N/M596L-APP (NL-APP), a mutant causing familial Alzheimer's disease (FAD), termed Swedish mutant, Transfection of neuronal cells with HN cDNA or treatment with the coding HN polypeptide abrogated cytotoxicity by NL-APP, HN suppressed neurotoxicity by A beta1-43 in the absence of N2 supplement, but could not inhibit AP secretion from NL-APP, HN could also protect neuronal cells from death by NL-APP lacking the 41st and 42nd residues of the A beta region, Therefore, HN suppressed neuronal cell death by NL-APP not through inhibition of A beta 42 secretion, but with two targets for its inhibitory action: (i) the intracellular toxic mechanism directly triggered by NL-APP and (ii) neurotoxicity by A beta. HN will contribute to the development of curative therapy of AD, especially as a novel reagent that could mechanistically supplement A beta -production inhibitors. (C) 2001 Academic Press.
引用
收藏
页码:460 / 468
页数:9
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