Literature DB >> 24240699

Mechanism and synergism in epithelial fluid and electrolyte secretion.

Jeong Hee Hong1, Seonghee Park, Nikolay Shcheynikov, Shmuel Muallem.   

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.

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Year:  2013        PMID: 24240699      PMCID: PMC4024104          DOI: 10.1007/s00424-013-1390-1

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  156 in total

1.  IRBIT, an inositol 1,4,5-trisphosphate receptor-binding protein, specifically binds to and activates pancreas-type Na+/HCO3- cotransporter 1 (pNBC1).

Authors:  Kyoko Shirakabe; Giuseppina Priori; Hideomi Yamada; Hideaki Ando; Shoko Horita; Toshiro Fujita; Ichiro Fujimoto; Akihiro Mizutani; George Seki; Katsuhiko Mikoshiba
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-12       Impact factor: 11.205

2.  Regulatory interaction between CFTR and the SLC26 transporters.

Authors:  Nikolay Shcheynikov; Shigeru B H Ko; Weizhong Zeng; Joo Young Choi; Michael R Dorwart; Philip J Thomas; Shmuel Muallem
Journal:  Novartis Found Symp       Date:  2006

Review 3.  Na+/H+ exchangers and the regulation of volume.

Authors:  R T Alexander; S Grinstein
Journal:  Acta Physiol (Oxf)       Date:  2006 May-Jun       Impact factor: 6.311

Review 4.  Calcium signaling complexes in microdomains of polarized secretory cells.

Authors:  Kirill Kiselyov; Xinhua Wang; Dong Min Shin; Weizhong Zang; Shmuel Muallem
Journal:  Cell Calcium       Date:  2006-10-10       Impact factor: 6.817

5.  IRBIT suppresses IP3 receptor activity by competing with IP3 for the common binding site on the IP3 receptor.

Authors:  Hideaki Ando; Akihiro Mizutani; Hélène Kiefer; Dai Tsuzurugi; Takayuki Michikawa; Katsuhiko Mikoshiba
Journal:  Mol Cell       Date:  2006-06-23       Impact factor: 17.970

6.  WNK4 kinase regulates surface expression of the human sodium chloride cotransporter in mammalian cells.

Authors:  H Cai; V Cebotaru; Y-H Wang; X-M Zhang; L Cebotaru; S E Guggino; W B Guggino
Journal:  Kidney Int       Date:  2006-05-10       Impact factor: 10.612

7.  WNK1 and WNK4 modulate CFTR activity.

Authors:  Chao-Ling Yang; Xuehong Liu; Alex Paliege; Xiaoman Zhu; Sebastian Bachmann; David C Dawson; David H Ellison
Journal:  Biochem Biophys Res Commun       Date:  2006-12-15       Impact factor: 3.575

8.  Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosis.

Authors:  Youxue Wang; Abigail A Soyombo; Nikolay Shcheynikov; Weizhong Zeng; Michael Dorwart; Christopher R Marino; Philip J Thomas; Shmuel Muallem
Journal:  EMBO J       Date:  2006-10-19       Impact factor: 11.598

9.  Regulation of the expression of the Na/Cl cotransporter by WNK4 and WNK1: evidence that accelerated dynamin-dependent endocytosis is not involved.

Authors:  Amir P Golbang; Georgina Cope; Abbas Hamad; Meena Murthy; Che-Hsiung Liu; Alan W Cuthbert; Kevin M O'shaughnessy
Journal:  Am J Physiol Renal Physiol       Date:  2006-06-20

Review 10.  Distribution and roles of aquaporins in salivary glands.

Authors:  Christine Delporte; Serge Steinfeld
Journal:  Biochim Biophys Acta       Date:  2006-02-28
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  23 in total

1.  Restoration of CFTR Activity in Ducts Rescues Acinar Cell Function and Reduces Inflammation in Pancreatic and Salivary Glands of Mice.

Authors:  Mei Zeng; Mitchell Szymczak; Malini Ahuja; Changyu Zheng; Hongen Yin; William Swaim; John A Chiorini; Robert J Bridges; Shmuel Muallem
Journal:  Gastroenterology       Date:  2017-06-19       Impact factor: 22.682

2.  The apical Na+ -HCO3 - cotransporter Slc4a7 (NBCn1) does not contribute to bicarbonate transport by mouse salivary gland ducts.

Authors:  Ning-Yan Yang; Taro Mukaibo; Ira Kurtz; James E Melvin
Journal:  J Cell Physiol       Date:  2019-02-14       Impact factor: 6.384

Review 3.  cAMP and Ca²⁺ signaling in secretory epithelia: crosstalk and synergism.

Authors:  Malini Ahuja; Archana Jha; Jozsef Maléth; Seonghee Park; Shmuel Muallem
Journal:  Cell Calcium       Date:  2014-02-07       Impact factor: 6.817

Review 4.  Cl- as a bona fide signaling ion.

Authors:  Benjamin P Lüscher; Laura Vachel; Ehud Ohana; Shmuel Muallem
Journal:  Am J Physiol Cell Physiol       Date:  2019-11-06       Impact factor: 4.249

5.  Insulin is involved in transcriptional regulation of NKCC and the CFTR Cl(-) channel through PI3K activation and ERK inactivation in renal epithelial cells.

Authors:  Hongxin Sun; Naomi Niisato; Toshio Inui; Yoshinori Marunaka
Journal:  J Physiol Sci       Date:  2014-09-20       Impact factor: 2.781

Review 6.  Regulation of epithelial ion transport in exocrine glands by store-operated Ca2+ entry.

Authors:  Axel R Concepcion; Stefan Feske
Journal:  Cell Calcium       Date:  2016-12-21       Impact factor: 6.817

7.  Transcriptional profiling reveals gland-specific differential expression in the three major salivary glands of the adult mouse.

Authors:  Xin Gao; Maria S Oei; Catherine E Ovitt; Murat Sincan; James E Melvin
Journal:  Physiol Genomics       Date:  2018-01-26       Impact factor: 3.107

Review 8.  Calcium signalling in salivary gland physiology and dysfunction.

Authors:  Indu S Ambudkar
Journal:  J Physiol       Date:  2015-12-15       Impact factor: 5.182

Review 9.  Pharmacological targeting of SPAK kinase in disorders of impaired epithelial transport.

Authors:  Jinwei Zhang; Jason K Karimy; Eric Delpire; Kristopher T Kahle
Journal:  Expert Opin Ther Targets       Date:  2017-07-12       Impact factor: 6.902

10.  Expression of the B splice variant of NBCe1 (SLC4A4) in the mouse kidney.

Authors:  Lijuan Fang; Hyun-Wook Lee; Chao Chen; Autumn N Harris; Michael F Romero; Jill W Verlander; I David Weiner
Journal:  Am J Physiol Renal Physiol       Date:  2018-04-04
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