A secreted form of human ADAM9 has an α-secretase activity for APP

被引:81
作者
Hotoda, N
Koike, H
Sasagawa, N
Ishiura, S
机构
[1] Univ Tokyo, Dept Life Sci, Grad Sch Arts & Sci, Meguro Ku, Tokyo 1538902, Japan
[2] Meiji Pharmaceut Univ, Dept Biochem, Tokyo 2048588, Japan
关键词
disintegrin metalloprotease; splicing form; amyloid precursor protein; alpha-secretase; proteolysis;
D O I
10.1016/S0006-291X(02)00302-9
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
ADAM9 (MDC9, meltrin gamma) is a member of the ADAM family of metalloproteases, which play important roles in cell-cell fusion. intracellular signaling, and other cellular functions. Here we cloned a novel form of human ADAM9, designated hADAM9s (s for short), which lacks the carboxyl-terminus. Human ADAM9s was found to be secreted from transfected COS cells. RT-PCR analysis demonstrated that the mRNA for hADAM9s is expressed in human brain, liver, heart. kidney, lung, and trachea. When hADAM9s was co-expressed in COS cells with APP and treated with phorbol ester. the APP was digested exclusively at the alpha-secretory site. These results suggest that hADAM9s has an alpha-secretase-like activity for APP. Non-amyloidgenic cleavage of APP may occur at the plasma membrane. Our new results support a new therapeutic strategy to decrease in the AP content by directly activating ADAM9 in the extracellular space. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:800 / 805
页数:6
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