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血小板活化因子在肠道上皮分泌及中国仓鼠卵巢细胞细胞骨架对霍乱毒素反应中的作用。

Role of platelet activating factor in the intestinal epithelial secretory and Chinese hamster ovary cell cytoskeletal responses to cholera toxin.

作者信息

Guerrant R L, Fang G D, Thielman N M, Fonteles M C

机构信息

Department of Medicine, University of Virginia, Charlottesville 22908.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9655-8. doi: 10.1073/pnas.91.20.9655.

Abstract

With the recent heightened concern about cholera around the world come new questions about the mechanism by which cholera toxin causes diarrhea. Peterson and Ochoa have suggested that prostaglandin synthesis is key to both the intestinal epithelial secretory and the CHO cell responses to cholera toxin [Peterson, J. W. and Ochoa, G. (1989) Science 245, 857-859]. Because platelet activating factor (PAF) can be a potent stimulus for prostaglandin synthesis, we examined its role in the intestinal and tissue culture effects of cholera toxin. We report that the specific PAF receptor antagonists BN 52021 and SR 27417 inhibit the effects of cholera toxin on intestinal secretion in rabbit ileal loops in vivo and on the cytoskeleton of Chinese hamster ovary cells in vitro. We also show that PAF itself can cause net fluid secretion in the rabbit model and that PAF potentiates the effects of cholera toxin on intestinal secretion. Finally, we demonstrate that cholera toxin stimulates significant PAF production (2.6-fold) in isolated T-84 intestinal epithelial cells. We conclude that cholera toxin stimulates PAF production and that PAF is involved in both the secretory and cytoskeletal responses to cholera toxin. These findings further support the involvement of additional mediators of cholera toxin effects other than mucosal cell cyclic AMP and help explain the effects of cholera toxin on prostaglandin synthesis.

摘要

随着近期全球对霍乱的关注度不断提高,关于霍乱毒素导致腹泻的机制出现了新的问题。彼得森和奥乔亚提出,前列腺素合成是肠道上皮分泌以及CHO细胞对霍乱毒素反应的关键[彼得森,J.W.和奥乔亚,G.(1989年)《科学》245,857 - 859]。由于血小板活化因子(PAF)可以是前列腺素合成的有效刺激物,我们研究了其在霍乱毒素对肠道和组织培养的影响中的作用。我们报告,特异性PAF受体拮抗剂BN 52021和SR 27417在体内抑制霍乱毒素对兔回肠袢肠道分泌的影响,在体外抑制其对中国仓鼠卵巢细胞细胞骨架的影响。我们还表明,PAF本身可在兔模型中引起净液体分泌,并且PAF增强霍乱毒素对肠道分泌的作用。最后,我们证明霍乱毒素在分离的T - 84肠道上皮细胞中刺激显著的PAF产生(2.6倍)。我们得出结论,霍乱毒素刺激PAF产生,并且PAF参与对霍乱毒素的分泌和细胞骨架反应。这些发现进一步支持了除粘膜细胞环磷酸腺苷之外的霍乱毒素效应的其他介质的参与,并有助于解释霍乱毒素对前列腺素合成的影响。

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