Inhibition of alanyl aminopeptidase induces MAP-Kinase p42/ERK2 in the human T cell line KARPAS-299

被引:34
作者
Lendeckel, U
Kähne, T
Arndt, M
Frank, K
Ansorge, S
机构
[1] Univ Magdeburg, Ctr Internal Med, Inst Expt Internal Med, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Inst Immunol, D-39120 Magdeburg, Germany
关键词
alanyl aminopeptidase; CD13; peptidase; peptidase inhibitor; cell proliferation; ERK2; MAP-kinase; quantitative PCR; Lightcycler;
D O I
10.1006/bbrc.1998.9585
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
Inhibition of alanyl aminopeptidase (EC 3.4.11.2, aminopeptidase N, CD13) expression, or activity compromise cell proliferation in a number of cell systems [1-6]. The underlying mechanisms and the molecular components involved have not been identified as yet. In this study we show that inhibition of alanyl aminopeptidase enzymatic activity decreases the proliferation rate of the CD13-positive T cell line Karpas-299. By using the ATLAS cDNA expression array (Clontech) we identified the p42/ERK2 MAP kinase as one downstream target of probestin, a potent inhibitor of alanyl aminopeptidase. Probestin and another specific aminopeptidase inhibitor, actinonin, in addition to their capability of inducing erk-2 mRNA levels, significantly increase p42 phosphorylation state. This is the first report on signal transduction components possibly mediating the growth-modulatory effects of alanyl aminopeptidase inhibitors. (C) 1998 Academic Press.
引用
收藏
页码:5 / 9
页数:5
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