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C6大鼠胶质瘤细胞中钙介导的内皮素信号传导

Calcium-mediated endothelin signaling in C6 rat glioma cells.

作者信息

Sedo A, Malík R, Vlăsicová K, Rovero P

机构信息

1st Institute of Medical Chemistry and Biochemistry, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Neuropeptides. 1999 Feb;33(1):13-7. doi: 10.1054/npep.1999.0025.

Abstract

Endothelin induced intracellular Ca(2+)signaling was studied in C6 rat glial cells. Endothelins 1 and 3 increased transiently intracellular Ca(2+)concentration, endothelin 3 being less potent inducer. Dibutyryl-cAMP treated cells responded with less sensitivity. While BQ123, a specific endothelin A receptor antagonist, inhibited both endothelins induced response in proliferating cells, it failed to inhibit in dibutyryl-cAMP treated ones. IRL1620, a specific endothelin B receptor agonist, was devoid of any significant effect. Although re-stimulation by both endothelins after endothelin-1 did not cause any Ca(2+)oscillation, both endothelins evoked new Ca(2+)transient after endothelin-3 stimulation. Our findings suggest that endothelin induced Ca(2+)signaling is mediated probably through the receptor A in proliferating C6 cells. The lack of both BQ123 and IRL 1620 effect in dibutyryl-cAMP treated cells could be caused by an alteration of endothelin A receptor alone, by a change of receptor expression pattern, or by more complex postreceptor mechanism.

摘要

在C6大鼠神经胶质细胞中研究了内皮素诱导的细胞内Ca(2+)信号传导。内皮素1和3可使细胞内Ca(2+)浓度短暂升高,内皮素3的诱导作用较弱。经二丁酰环磷腺苷(dibutyryl-cAMP)处理的细胞反应敏感性较低。特异性内皮素A受体拮抗剂BQ123可抑制增殖细胞中两种内皮素诱导的反应,但对经二丁酰环磷腺苷处理的细胞则无抑制作用。特异性内皮素B受体激动剂IRL1620无明显作用。虽然内皮素-1后再用两种内皮素刺激均未引起任何Ca(2+)振荡,但内皮素-3刺激后两种内皮素均引发了新的Ca(2+)瞬变。我们的研究结果表明,在增殖的C6细胞中,内皮素诱导的Ca(2+)信号传导可能通过受体A介导。在经二丁酰环磷腺苷处理的细胞中,BQ123和IRL 1620均无作用,这可能是由于内皮素A受体单独改变、受体表达模式改变或更复杂的受体后机制所致。

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