Rockey D C
Liver Center Laboratory, University of California, San Francisco.
Biochem Biophys Res Commun. 1995 Feb 15;207(2):725-31. doi: 10.1006/bbrc.1995.1247.
Hepatic stellate cells (Ito cells) are perisinusoidal cells with features typical of tissue pericytes which have been implicated in the modulation of sinusoidal blood flow. They possess endothelin (ET) receptors and contract in response to ETs. To elucidate the role of ET receptors in stellate cell contraction, a model cell contraction system was used to examine the effect of ET-1, ET-3, sarafotoxin S6C (a pure ETB receptor agonist) and ETA and/or ETB receptor antagonists. ET-1 and sarafotoxin S6C elicited similar contractile responses (EC50 0.18 and 0.21 nM, respectively). BQ-123, an ETA antagonist, minimally inhibited ET-1 induced contraction, while bosentan, a mixed, nonpeptide ETA/ETB antagonist, inhibited ET-1 and sarafotoxin S6C mediated contraction in a similar fashion. In contrast, bosentan had little effect on ET-3 stimulated contraction. The data demonstrate that the ETB receptor is a prominent mediator of stellate cell contraction and raise the possibility of a novel ET receptor subtype.
肝星状细胞(伊托细胞)是位于肝血窦周围的细胞,具有组织周细胞的典型特征,参与调节肝血窦血流。它们具有内皮素(ET)受体,并能对ET产生收缩反应。为了阐明ET受体在星状细胞收缩中的作用,我们使用了一个细胞收缩模型系统来研究ET-1、ET-3、铃蟾毒素S6C(一种纯ETB受体激动剂)以及ETA和/或ETB受体拮抗剂的作用。ET-1和铃蟾毒素S6C引发了相似的收缩反应(EC50分别为0.18和0.21 nM)。ETA拮抗剂BQ-123对ET-1诱导的收缩作用微弱,而混合性非肽ETA/ETB拮抗剂波生坦则以相似的方式抑制ET-1和铃蟾毒素S6C介导的收缩。相反,波生坦对ET-3刺激的收缩作用很小。这些数据表明,ETB受体是星状细胞收缩的主要介质,并提示存在一种新型ET受体亚型的可能性。