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大肠杆菌肠毒素受体:在负鼠肾脏、肠道和睾丸中的定位。

Escherichia coli enterotoxin receptors: localization in opossum kidney, intestine, and testis.

作者信息

Forte L R, Krause W J, Freeman R H

机构信息

Department of Pharmacology, School of Medicine, University of Missouri, Columbia.

出版信息

Am J Physiol. 1989 Nov;257(5 Pt 2):F874-81. doi: 10.1152/ajprenal.1989.257.5.F874.

Abstract

The distribution of receptors for Escherichia coli enterotoxin were examined in opossum kidney, intestine, and testis. E. coli enterotoxin stimulated guanosine 3',5'-cyclic monophosphate (cGMP) production in renal cortex, testis, and small intestinal mucosa but had only a small effect in the colon. Atrial natriuretic factor enhanced the cGMP content of renal cortex and small intestine but had no effect on testis or colon. The enterotoxin receptors were observed to be localized in proximal tubules, to epithelial cells of crypts and villi of small intestine, to crypts of colon, and in seminiferous tubules. Both convoluted and straight portions of proximal tubules exhibited specific binding sites for 125I-labeled enterotoxin. Glomeruli and distal tubules did not have receptors. Binding of 125I-enterotoxin to brush-border membranes of kidney cortex or intestinal mucosa and to testis membranes was markedly temperature dependent. The binding affinities of these receptors for E. coli enterotoxin were similar (i.e., IC50 approximately equal to 0.4-0.5 nM). Daily administration of 20 micrograms of enterotoxin intramuscularly to opossums increased urine cGMP excretion with no apparent changes in urine volume, Na+, or K+ excretion. Thus receptors for heat-stable enterotoxins are localized to proximal tubules of kidney and to enterocytes and seminiferous tubules of intestine and testis, respectively. Apical membranes may be the site of enterotoxin receptors in these epithelia.

摘要

研究了负鼠肾脏、肠道和睾丸中大肠杆菌肠毒素受体的分布情况。大肠杆菌肠毒素可刺激肾皮质、睾丸和小肠黏膜中鸟苷 3',5'-环磷酸(cGMP)的产生,但对结肠的影响较小。心房利钠因子可提高肾皮质和小肠中的 cGMP 含量,但对睾丸或结肠无影响。观察到肠毒素受体定位于近端小管、小肠隐窝和绒毛的上皮细胞、结肠隐窝以及生精小管。近端小管的曲部和直部均显示出对 125I 标记肠毒素的特异性结合位点。肾小球和远端小管没有受体。125I 肠毒素与肾皮质或肠黏膜刷状缘膜以及睾丸膜的结合明显依赖于温度。这些受体对大肠杆菌肠毒素的结合亲和力相似(即半数抑制浓度约等于 0.4 - 0.5 nM)。每天给负鼠肌肉注射 20 微克肠毒素可增加尿 cGMP 排泄量,而尿量、Na+或 K+排泄量无明显变化。因此,热稳定肠毒素的受体分别定位于肾脏的近端小管以及肠道和睾丸的肠上皮细胞和生精小管。顶端膜可能是这些上皮细胞中肠毒素受体的所在部位。

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