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首页> 外文期刊>The Biochemical Journal >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
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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

机译:磷脂酰肌醇转移蛋白与磷酸肌醇3-激酶γ在人嗜中性粒细胞的甲酰甲硫氨酰-亮氨酰苯丙氨酸依赖性磷脂酰肌醇3,4,5-三磷酸生成中的协同作用

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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 P13K 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.
机译:磷酸肌醇3-激酶(PI3K)及其产物磷脂酰肌醇3,4,5-三磷酸酯(PIP3)在化学引诱剂甲酰甲硫酰基-亮氨酰苯丙氨酸(FMLP)的中性粒细胞功能调节中起重要作用。在这里,我们显示人类嗜中性粒细胞的通透性导致包括P13Kγ在内的胞质成分的损失,并导致FMLP依赖的PIP3产生的损失。 FMLP敏感的PIP3合成可以通过用重组PI3Kγ重建通透性中性粒细胞来恢复,重组磷脂酰肌醇转移蛋白(PITP)与重组鸡尾酒的混合物进一步增加了PIP3的合成,而百日咳毒素抑制了FMLP依赖性的PIP3。我们得出的结论是,人类嗜中性粒细胞中FMLP敏感的PIP3的形成涉及FMLP受体,G(i)型异三聚体G蛋白,PI3Kγ和PITP。

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