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c-Src和蛋白激酶Cδ参与血清素对Caco-2细胞中Cl(-)/OH-交换活性的抑制作用。

Involvement of c-Src and protein kinase C delta in the inhibition of Cl(-)/OH- exchange activity in Caco-2 cells by serotonin.

作者信息

Saksena Seema, Gill Ravinder K, Tyagi Sangeeta, Alrefai Waddah A, Sarwar Zaheer, Ramaswamy Krishnamurthy, Dudeja Pradeep K

机构信息

Section of Digestive Diseases and Nutrition, Department of Medicine, University of Illinois and Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois 60612, USA.

出版信息

J Biol Chem. 2005 Mar 25;280(12):11859-68. doi: 10.1074/jbc.M411553200. Epub 2005 Jan 6.

Abstract

Serotonin (5-hydroxytryptamine (5-HT)) is an important neurotransmitter and intercellular messenger regulating various gastrointestinal functions, including electrolyte transport. To date, however, no information is available with respect to its effects on the human intestinal apical anion exchanger Cl(-)/OH- (HCO3-). The present studies were therefore undertaken to examine the direct effects of serotonin on OH- gradient-driven 4,4'-diisothiocyanato-stilbene-2, 2'-disulfonic acid-sensitive 36Cl- uptake utilizing the post-confluent transformed human intestinal epithelial cell line Caco-2. Our results demonstrate that serotonin inhibits Cl(-)/OH- exchange activity in Caco-2 cells via both tyrosine kinase and Ca(2+)-independent protein kinase C delta-mediated pathways involving either 5-HT3 or 5-HT4 receptor subtype. The data consistent with our inference are as follows. (i) The short term treatment of cells with 5-HT (0.1 microM) for 15-60 min significantly decreased Cl(-)/OH- exchange (50-70%, p < 0.05). (ii) The specific agonists for 5-HT3, m-chlorophenylbiguanide, and 5-HT4, 3-(4-allylpiperazin-1-yl)-2-quinoxaline chloronitrile, mimicked the effects of serotonin. (iii) Tropisetron dual inhibitor for both the 5-HT3/4 receptor subtypes significantly blocked the inhibition, whereas specific 5-HT3 (Y-25130) or 5-HT4 receptor (RS39604) antagonist failed to block the inhibitory effects of 5-HT. (iv) The Ca2+ chelator 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl ester) had no effect on the serotonin-induced inhibition. (v) The specific protein kinase C (PKC) inhibitors chelerythrine chloride or calphostin C completely blocked the inhibition by 5-HT. (vi) The specific inhibitor for PKC delta, rottlerin, significantly blocked the inhibition by 5-HT. (vii) The specific tyrosine kinase inhibitor, herbimycin, or Src family kinase inhibitor, PP1, abolished the 5-HT-mediated inhibition of Cl(-)/OH- exchange activity. (viii) 5-HT stimulated tyrosine phosphorylation of c-Src kinase and PKC delta.

摘要

血清素(5-羟色胺(5-HT))是一种重要的神经递质和细胞间信使,可调节包括电解质转运在内的各种胃肠功能。然而,迄今为止,尚无关于其对人肠顶端阴离子交换体Cl(-)/OH-(HCO3-)作用的信息。因此,本研究采用汇合后转化的人肠上皮细胞系Caco-2,研究血清素对OH-梯度驱动的4,4'-二异硫氰酸根合芪-2,2'-二磺酸敏感的36Cl-摄取的直接影响。我们的结果表明,血清素通过涉及5-HT3或5-HT4受体亚型的酪氨酸激酶和不依赖Ca(2+)的蛋白激酶Cδ介导的途径,抑制Caco-2细胞中的Cl(-)/OH-交换活性。与我们推断一致的数据如下:(i)用5-HT(0.1微摩尔)对细胞进行15至60分钟的短期处理,可显著降低Cl(-)/OH-交换(50-70%,p<0.05)。(ii)5-HT3的特异性激动剂间氯苯双胍和5-HT4的特异性激动剂3-(4-烯丙基哌嗪-1-基)-2-喹喔啉腈可模拟血清素的作用。(iii)5-HT3/4受体亚型的双重抑制剂托烷司琼可显著阻断这种抑制作用,而特异性5-HT3(Y-25130)或5-HT4受体(RS39604)拮抗剂未能阻断5-HT的抑制作用。(iv)Ca2+螯合剂1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸四(乙酰氧基甲酯)对血清素诱导的抑制作用无影响。(v)特异性蛋白激酶C(PKC)抑制剂氯化白屈菜红碱或钙泊三醇可完全阻断5-HT的抑制作用。(vi)PKCδ的特异性抑制剂rottlerin可显著阻断5-HT的抑制作用。(vii)特异性酪氨酸激酶抑制剂赫曲霉素或Src家族激酶抑制剂PP1可消除5-HT介导的Cl(-)/OH-交换活性抑制作用。(viii)5-HT刺激c-Src激酶和PKCδ的酪氨酸磷酸化。

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