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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Lysophospholipids regulate excitability and exocytosis in cultured bovine chromaffin cells.
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Lysophospholipids regulate excitability and exocytosis in cultured bovine chromaffin cells.

机译:溶血磷脂调节培养的牛嗜铬细胞的兴奋性和胞吐作用。

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Bioactive lysophospholipids (LPLs) are released by blood cells and can modulate many cellular activities such as angiogenesis and cell survival. In this study, the effects of sphingosine-1-phosphate (S1P) and lysophosphatidic acid (LPA) on excitability and exocytosis in bovine chromaffin cells were investigated using the whole-cell configuration of the patch-clamp. Voltage-gated Ca(2+) current was inhibited by S1P and LPA pre-treatment in a concentration-dependent manner with IC(50)s of 0.46 and 0.79 mumol/L, respectively. Inhibition was mostly reversible upon washout and prevented by suramin, an inhibitor of G-protein signaling. Na(+) current was inhibited by S1P, but not by LPA. However, recovery of Na(+) channels from inactivation was slowed by both LPLs. The outward K(+) current was also significantly reduced by both LPLs. Chromaffin cells fired repetitive action potentials in response to minimal injections of depolarizing current. Repetitive activity was dramatically reduced by LPLs. Consistent with the reduction in Ca(2+) current, exocytosis elicited by a train of depolarizations and the ensuing endocytosis were both inhibited by LPL pre-treatments. These data demonstrate the interaction between immune and endocrine systems mediated by the inhibitory effects of LPLs on the excitability of adrenal chromaffin cells.
机译:血细胞释放出生物活性的溶血磷脂(LPL),可以调节许多细胞活性,例如血管生成和细胞存活。在这项研究中,使用膜片钳的全细胞构型研究了鞘氨醇-1-磷酸鞘氨醇(S1P)和溶血磷脂酸(LPA)对牛嗜铬细胞兴奋性和胞吐作用的影响。 S1P和LPA预处理以浓度依赖的方式抑制电压门控的Ca(2+)电流,IC(50)的浓度分别为0.46和0.79 mumol / L。抑制作用在洗脱后大部分是可逆的,被苏拉明(一种G蛋白信号抑制剂)阻止。 Na(+)电流受S1P抑制,但不受LPA抑制。但是,两个LPL均使失活的Na(+)通道恢复缓慢。两个LPL也显着降低了向外的K(+)电流。响应于极少的去极化电流注入,嗜铬细胞释放出重复动作电位。 LPL大大减少了重复活动。与减少Ca(2+)电流一致,通过一系列去极化引发的胞吐作用和随之而来的内吞作用均受到LPL预处理的抑制。这些数据表明,LPL对肾上腺嗜铬细胞兴奋性的抑制作用介导了免疫系统和内分泌系统之间的相互作用。

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