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在过表达凝溶胶蛋白的NIH 3T3成纤维细胞中缓激肽和1-磷酸鞘氨醇对磷脂酶D的差异性激活作用

Differential phospholipase D activation by bradykinin and sphingosine 1-phosphate in NIH 3T3 fibroblasts overexpressing gelsolin.

作者信息

Banno Y, Fujita H, Ono Y, Nakashima S, Ito Y, Kuzumaki N, Nozawa Y

机构信息

Department of Biochemistry, Gifu University School of Medicine, Tsukasamachi-40, Gifu 500-8705, Japan.

出版信息

J Biol Chem. 1999 Sep 24;274(39):27385-91. doi: 10.1074/jbc.274.39.27385.

Abstract

Gelsolin, an actin-binding protein, shows a strong ability to bind to phosphatidylinositol 4,5-bisphosphate (PIP(2)). Here we showed in in vitro experiments that gelsolin inhibited recombinant phospholipase D1 (PLD1) and PLD2 activities but not the oleate-dependent PLD and that this inhibition was not reversed by increasing PIP(2) concentration. To investigate the role of gelsolin in agonist-mediated PLD activation, we used NIH 3T3 fibroblasts stably transfected with the cDNA for human cytosolic gelsolin. Gelsolin overexpression suppressed bradykinin-induced activation of phospholipase C (PLC) and PLD. On the other hand, sphingosine 1-phosphate (S1P)-induced PLD activation could not be modified by gelsolin overexpression, whereas PLC activation was suppressed. PLD activation by phorbol myristate acetate or Ca(2+) ionophore A23187 was not affected by gelsolin overexpression. Stimulation of control cells with either bradykinin or S1P caused translocation of protein kinase C (PKC) to the membranes. Translocation of PKC-alpha and PKC-beta1 but not PKC-epsilon was reduced in gelsolin-overexpressed cells, whereas phosphorylation of mitogen-activated protein kinase was not changed. S1P-induced PLC activation and mitogen-activated protein kinase phosphorylation were sensitive to pertussis toxin, but PLD response was insensitive to such treatment, suggesting that S1P induced PLD activation via certain G protein distinct from G(i) for PLC and mitogen-activated protein kinase pathway. Our results suggest that gelsolin modulates bradykinin-mediated PLD activation via suppression of PLC and PKC activities but did not affect S1P-mediated PLD activation.

摘要

凝溶胶蛋白是一种肌动蛋白结合蛋白,具有很强的结合磷脂酰肌醇4,5 - 二磷酸(PIP₂)的能力。我们在此展示的体外实验表明,凝溶胶蛋白可抑制重组磷脂酶D1(PLD1)和PLD2的活性,但不抑制油酸依赖性磷脂酶D,且这种抑制作用不会因增加PIP₂浓度而逆转。为了研究凝溶胶蛋白在激动剂介导的磷脂酶D激活中的作用,我们使用了稳定转染人胞质凝溶胶蛋白cDNA的NIH 3T3成纤维细胞。凝溶胶蛋白的过表达抑制了缓激肽诱导的磷脂酶C(PLC)和磷脂酶D的激活。另一方面,鞘氨醇1 - 磷酸(S1P)诱导的磷脂酶D激活不受凝溶胶蛋白过表达的影响,而PLC激活受到抑制。佛波醇肉豆蔻酸酯乙酸盐或Ca²⁺离子载体A23187诱导的磷脂酶D激活不受凝溶胶蛋白过表达的影响。用缓激肽或S1P刺激对照细胞会导致蛋白激酶C(PKC)转位至细胞膜。在凝溶胶蛋白过表达的细胞中,PKC - α和PKC - β1的转位减少,但PKC - ε未减少,而丝裂原活化蛋白激酶的磷酸化没有变化。S1P诱导的PLC激活和丝裂原活化蛋白激酶磷酸化对百日咳毒素敏感,但磷脂酶D反应对这种处理不敏感,这表明S1P通过不同于PLC和丝裂原活化蛋白激酶途径的G(i)的某些G蛋白诱导磷脂酶D激活。我们的结果表明,凝溶胶蛋白通过抑制PLC和PKC活性来调节缓激肽介导的磷脂酶D激活,但不影响S1P介导的磷脂酶D激活。

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