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上皮细胞液体和电解质分泌的机制与协同作用。

Mechanism and synergism in epithelial fluid and electrolyte secretion.

作者信息

Hong Jeong Hee, Park Seonghee, Shcheynikov Nikolay, Muallem Shmuel

机构信息

Epithelial Signaling and Transport Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institute of Health, Bethesda, MD, 20892, USA.

出版信息

Pflugers Arch. 2014 Aug;466(8):1487-99. doi: 10.1007/s00424-013-1390-1. Epub 2013 Nov 16.

Abstract

A central function of epithelia is the control of the volume and electrolyte composition of bodily fluids through vectorial transport of electrolytes and the obligatory H2O. In exocrine glands, fluid and electrolyte secretion is carried out by both acinar and duct cells, with the portion of fluid secreted by each cell type varying among glands. All acinar cells secrete isotonic, plasma-like fluid, while the duct determines the final electrolyte composition of the fluid by absorbing most of the Cl(-) and secreting HCO3 (-). The key transporters mediating acinar fluid and electrolyte secretion are the basolateral Na(+)/K(+) /2Cl(-) cotransporter, the luminal Ca(2+)-activated Cl(-) channel ANO1 and basolateral and luminal Ca(2+)-activated K(+) channels. Ductal fluid and HCO3 (-) secretion are mediated by the basolateral membrane Na(+)-HCO3 (-) cotransporter NBCe1-B and the luminal membrane Cl(-)/HCO3 (-) exchanger slc26a6 and the Cl(-) channel CFTR. The function of the transporters is regulated by multiple inputs, which in the duct include major regulation by the WNK/SPAK pathway that inhibit secretion and the IRBIT/PP1 pathway that antagonize the effects of the WNK/SPAK pathway to both stimulate and coordinate the secretion. The function of these regulatory pathways in secretory glands acinar cells is yet to be examined. An important concept in biology is synergism among signaling pathways to generate the final physiological response that ensures regulation with high fidelity and guards against cell toxicity. While synergism is observed in all epithelial functions, the molecular mechanism mediating the synergism is not known. Recent work reveals a central role for IRBIT as a third messenger that integrates and synergizes the function of the Ca(2+) and cAMP signaling pathways in activation of epithelial fluid and electrolyte secretion. These concepts are discussed in this review using secretion by the pancreatic and salivary gland ducts as model systems.

摘要

上皮组织的一个核心功能是通过电解质和必需的H2O的矢量运输来控制体液的体积和电解质组成。在外分泌腺中,液体和电解质分泌由腺泡细胞和导管细胞共同完成,每种细胞类型分泌的液体比例在不同腺体中有所不同。所有腺泡细胞分泌等渗的、类似血浆的液体,而导管则通过吸收大部分Cl(-)并分泌HCO3 (-)来决定液体的最终电解质组成。介导腺泡液体和电解质分泌的关键转运体是基底外侧Na(+)/K(+)/2Cl(-)协同转运体、管腔Ca(2+)激活的Cl(-)通道ANO1以及基底外侧和管腔Ca(2+)激活的K(+)通道。导管液体和HCO3 (-)分泌由基底外侧膜Na(+)-HCO3 (-)协同转运体NBCe1-B、管腔膜Cl(-)/HCO3 (-)交换体slc26a6和Cl(-)通道CFTR介导。这些转运体的功能受到多种输入的调节,在导管中,主要由抑制分泌的WNK/SPAK途径和拮抗WNK/SPAK途径作用以刺激和协调分泌的IRBIT/PP1途径调节。这些调节途径在分泌腺腺泡细胞中的功能尚待研究。生物学中的一个重要概念是信号通路之间的协同作用,以产生最终的生理反应,确保高保真调节并防止细胞毒性。虽然在所有上皮功能中都观察到了协同作用,但其介导协同作用的分子机制尚不清楚。最近的研究揭示了IRBIT作为第三信使的核心作用,它整合并协同Ca(2+)和cAMP信号通路在上皮液体和电解质分泌激活中的功能。本文以胰腺和唾液腺导管分泌为模型系统对这些概念进行了讨论。

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本文引用的文献

1
SLC26A6 and NaDC-1 transporters interact to regulate oxalate and citrate homeostasis.
J Am Soc Nephrol. 2013 Oct;24(10):1617-26. doi: 10.1681/ASN.2013010080. Epub 2013 Jul 5.
3
The conserved tetrameric subunit stoichiometry of Slc26 proteins.
Microsc Microanal. 2013 Aug;19(4):799-807. doi: 10.1017/S1431927613000457. Epub 2013 May 3.
4
Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4.
Proc Natl Acad Sci U S A. 2013 May 7;110(19):7838-43. doi: 10.1073/pnas.1304592110. Epub 2013 Apr 1.
5
Molecular targeting of Gα and Gβγ subunits: a potential approach for cancer therapeutics.
Trends Pharmacol Sci. 2013 May;34(5):290-8. doi: 10.1016/j.tips.2013.02.006. Epub 2013 Apr 1.
6
Irbit mediates synergy between ca(2+) and cAMP signaling pathways during epithelial transport in mice.
Gastroenterology. 2013 Jul;145(1):232-241. doi: 10.1053/j.gastro.2013.03.047. Epub 2013 Mar 28.
7
Crossing paths: cytokinin signalling and crosstalk.
Development. 2013 Apr;140(7):1373-83. doi: 10.1242/dev.086371.
8
Impaired KLHL3-mediated ubiquitination of WNK4 causes human hypertension.
Cell Rep. 2013 Mar 28;3(3):858-68. doi: 10.1016/j.celrep.2013.02.024. Epub 2013 Feb 28.
9
Convergence of IRBIT, phosphatidylinositol (4,5) bisphosphate, and WNK/SPAK kinases in regulation of the Na+-HCO3- cotransporters family.
Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):4105-10. doi: 10.1073/pnas.1221410110. Epub 2013 Feb 19.

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