Co-operation of phosphatidylinositol transfer protein with phosphoinositide 3-kinase gamma in the formylmethionyl-leucylphenylalanine-dependent production of phosphatidylinositol 3,4,5-trisphosphate in human neutrophils

被引:50
|
作者
Kular, G
Loubtchenkov, M
Swigart, P
Whatmore, J
Ball, A
Cockcroft, S
Wetzker, R
机构
[1] UNIV JENA, FAC MED, MAX PLANCK RES UNIT MOL CELL BIOL, D-07747 JENA, GERMANY
[2] UNIV LONDON UNIV COLL, DEPT PHYSIOL, LONDON WC1E 6JJ, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1042/bj3250299
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
Phosphoinositide 3-kinase (PI3K) and its product phosphatidylinositol 3,4,5-trisphosphate (PIP3) play an essential role in the regulation of neutrophil functions by the chemoattractant formylmethionyl-leucylphenylalanine (FMLP). Here we show that permeabilization of human neutrophils leads to loss of cytosolic components, including PI3K gamma, and causes the loss of FMLP-dependent production of PIP3. FMLP-sensitive synthesis of PIP3 could be restored by reconstitution of permeabilized neutrophils with recombinant PI3K gamma, Admixture of recombinant phosphatidylinositol transfer protein (PITP) to the reconstitution cocktail produced a further increase of PIP3 synthesis, whereas pertussis toxin suppressed the FMLP-dependent production of PIP3. We conclude that FMLP-sensitive PIP3 formation in human neutrophils involves the FMLP receptor, heterotrimeric G-proteins of the G(i) type, PI3K gamma and PITP.
引用
收藏
页码:299 / 301
页数:3
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