Phosphatidic acid-mediated regulation of neutrophil plasma membrane CD45 phosphotyrosine phosphatase

被引:7
作者
Cui, Y [1 ]
English, DK [1 ]
机构
[1] INDIANA UNIV, SCH MED, SCH ALLIED HLTH SCI, INDIANAPOLIS, IN USA
基金
美国国家卫生研究院;
关键词
neutrophils; signal transduction; phosphatidic acid; protein tyrosine phosphatase; CD45;
D O I
10.1016/S0898-6568(96)00177-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CD45-phosphotyrosine phosphatase (PTPase) constitutes the major portion of the PTPase activity within plasma membranes of neutrophilic leukocytes, where it regulates signals leading to functional activation. We have previously demonstrated that the catalytic component of neutrophil plasma membrane CD45-PTPase is regulated by a cytosolic inactivator which itself is attenuated upon cellular stimulation, allowing enzyme translocated from granule stores to express full activity. The present study investigated mechanisms of cytosolic inactivator attenuation. Preincubation of plasma membranes of stimulated neutrophils with cytosol from resting cells resulted in a rapid loss of membrane associated PTPase activity. Phosphatidic acid had no direct effect on plasma membrane PTPase activity but blunted in a dose dependent manner the effects of the PTPase inactivator. Inactivator attenuation was not observed with equivalent concentrations of either diacylglycerol or lysophosphatidic acid. Optimal attenuation of inactivator activity was obtained with long chain, soluble ligands, such as dicapryl phosphatidic acid. Inhibitors of neutrophil plasma membrane ecto-phosphatidic acid phosphohydrolase did not block inactivator attenuation, suggesting that phosphatidic acid and not one of its metabolites was the entity responsible. In conclusion, neutrophil plasma membrane PTPase is dynamically regulated by a cytosolic inactivator, the inhibition of which may potentiate the effects of PTPase translocated during cellular stimulation. Phosphatidic acid generated as a consequence of cellular stimulation may mediate this inhibition and thereby regulate the effects of tyrosine kinases activated during the initial phases of cell stimulation. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:257 / 263
页数:7
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