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本文引用的文献

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ANP and CNP activate CFTR expressed in Xenopus laevis oocytes by direct activation of PKA.心钠素(ANP)和C型钠尿肽(CNP)通过直接激活蛋白激酶A(PKA)来激活非洲爪蟾卵母细胞中表达的囊性纤维化跨膜传导调节因子(CFTR)。
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cGMP inhibition of type 3 phosphodiesterase is the major mechanism by which C-type natriuretic peptide activates CFTR in the shark rectal gland.cGMP 抑制型 3 磷酸二酯酶是 C 型利钠肽在鲨鱼直肠腺中激活 CFTR 的主要机制。
Am J Physiol Cell Physiol. 2014 Feb 15;306(4):C343-53. doi: 10.1152/ajpcell.00326.2013. Epub 2013 Nov 20.
3
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Science. 1960 Mar 4;131(3401):670-1. doi: 10.1126/science.131.3401.670.
8
The cellular mechanisms of Cl- secretion induced by C-type natriuretic peptide (CNP). Experiments on isolated in vitro perfused rectal gland tubules of Squalus acanthias.C型利钠肽(CNP)诱导的氯离子分泌的细胞机制。对尖吻角鲨离体灌注直肠腺小管进行的实验。
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Cloning, characterization, and functional expression of a CNP receptor regulating CFTR in the shark rectal gland.鲨鱼直肠腺中一种调节囊性纤维化跨膜传导调节因子(CFTR)的C型利钠肽(CNP)受体的克隆、特性鉴定及功能表达
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10
Vasoactive intestinal peptide, forskolin, and genistein increase apical CFTR trafficking in the rectal gland of the spiny dogfish, Squalus acanthias. Acute regulation of CFTR trafficking in an intact epithelium.血管活性肠肽、福斯高林和染料木黄酮可增加棘鲨(Squalus acanthias)直肠腺顶端囊性纤维化跨膜传导调节因子(CFTR)的转运。完整上皮中CFTR转运的急性调节。
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鲨鱼直肠腺模型:通过囊性纤维化跨膜传导调节因子实现受体介导的氯离子分泌的典范

THE SHARK RECTAL GLAND MODEL: A CHAMPION OF RECEPTOR MEDIATED CHLORIDE SECRETION THROUGH CFTR.

作者信息

Forrest John N

机构信息

NEW HAVEN, CONNECTICUT.

出版信息

Trans Am Clin Climatol Assoc. 2016;127:162-175.

PMID:28066051
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5216465/
Abstract

The dogfish shark salt gland was predicted by Smith and discovered by Burger at the Mount Desert Island Biological Laboratory in Salisbury Cove, Maine. It is an epithelial organ in the intestine composed of tubules that serve a single function: the secretion of hypertonic NaCl. Many G protein receptors are present on the basolateral surface of these tubules, including stimulatory receptors for vasoactive intestinal peptide, adenosine A, growth hormone releasing hormone, and inhibitory receptors for somatostatin and adenosine A. An entirely different class of stimulatory receptors is present as C-type natriuretic peptide receptors. Each stimulatory receptor evokes powerful NaCl secretion. G protein receptors bind to G to activate the catalytic unit of adenylate cyclase to form cyclic adenosine monophosphate (cAMP) and protein kinase A that phosphorylates the regulatory domain of cystic fibrosis transmembrane conductance regulator, opening the channel. The C-type natriuretic peptide receptor stimulates by activating guanylate cyclase and endogenous cyclic guanosine monophosphate which inhibits type 3 phosphodiesterase, the enzyme that breaks down cAMP, thereby elevating cAMP and activating the protein kinase A pathway.

摘要

角鲨的盐腺由史密斯预测,并由伯格在缅因州索尔兹伯里湾的芒特迪瑟特岛生物实验室发现。它是肠道中的一个上皮器官,由具有单一功能的小管组成:分泌高渗氯化钠。这些小管的基底外侧表面存在许多G蛋白受体,包括血管活性肠肽、腺苷A、生长激素释放激素的刺激受体,以及生长抑素和腺苷A的抑制受体。另一类完全不同的刺激受体是C型利钠肽受体。每种刺激受体都会引发强大的氯化钠分泌。G蛋白受体与G结合,激活腺苷酸环化酶的催化单位,形成环磷酸腺苷(cAMP)和蛋白激酶A,蛋白激酶A使囊性纤维化跨膜传导调节因子的调节域磷酸化,打开通道。C型利钠肽受体通过激活鸟苷酸环化酶和内源性环磷酸鸟苷来刺激,内源性环磷酸鸟苷抑制3型磷酸二酯酶,即分解cAMP的酶,从而提高cAMP并激活蛋白激酶A途径。