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Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation

Na(+)K(+)2Cl(−) co-transporters (NKCCs) effect the electroneutral movement of Na(+)-K(+) and 2Cl(−) ions across the plasma membrane of vertebrate cells. There are two known NKCC isoforms, NKCC1 (Slc12a2) and NKCC2 (Slc12a1). NKCC1 is a ubiquitously expressed transporter involved in cell volume regul...

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Autores principales: Singh, Richa, Kursan, Shams, Almiahoub, Mohamed Y., Almutairi, Mohammed M., Garzón-Muvdi, Tomás, Alvarez-Leefmans, Francisco J., Di Fulvio, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209364/
https://www.ncbi.nlm.nih.gov/pubmed/28101499
http://dx.doi.org/10.3389/fcell.2016.00150
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author Singh, Richa
Kursan, Shams
Almiahoub, Mohamed Y.
Almutairi, Mohammed M.
Garzón-Muvdi, Tomás
Alvarez-Leefmans, Francisco J.
Di Fulvio, Mauricio
author_facet Singh, Richa
Kursan, Shams
Almiahoub, Mohamed Y.
Almutairi, Mohammed M.
Garzón-Muvdi, Tomás
Alvarez-Leefmans, Francisco J.
Di Fulvio, Mauricio
author_sort Singh, Richa
collection PubMed
description Na(+)K(+)2Cl(−) co-transporters (NKCCs) effect the electroneutral movement of Na(+)-K(+) and 2Cl(−) ions across the plasma membrane of vertebrate cells. There are two known NKCC isoforms, NKCC1 (Slc12a2) and NKCC2 (Slc12a1). NKCC1 is a ubiquitously expressed transporter involved in cell volume regulation, Cl(−) homeostasis and epithelial salt secretion, whereas NKCC2 is abundantly expressed in kidney epithelial cells of the thick ascending loop of Henle, where it plays key roles in NaCl reabsorption and electrolyte homeostasis. Although NKCC1 and NKCC2 co-transport the same ions with identical stoichiometry, NKCC1 actively co-transports water whereas NKCC2 does not. There is growing evidence showing that NKCC2 is expressed outside the kidney, but its function in extra-renal tissues remains unknown. The present study shows molecular and functional evidence of endogenous NKCC2 expression in COS7 cells, a widely used mammalian cell model. Endogenous NKCC2 is primarily found in recycling endosomes, Golgi cisternae, Golgi-derived vesicles, and to a lesser extent in the endoplasmic reticulum. Unlike NKCC1, NKCC2 is minimally hybrid/complex N-glycosylated under basal conditions and yet it is trafficked to the plasma membrane region of hyper-osmotically challenged cells through mechanisms that require minimal complex N-glycosylation or functional Golgi cisternae. Control COS7 cells exposed to slightly hyperosmotic (~6.7%) solutions for 16 h were not shrunken, suggesting that either one or both NKCC1 and NKCC2 may participate in cell volume recovery. However, NKCC2 targeted to the plasma membrane region or transient over-expression of NKCC2 failed to rescue NKCC1 in COS7 cells where NKCC1 had been silenced. Further, COS7 cells in which NKCC1, but not NKCC2, was silenced exhibited reduced cell size compared to control cells. Altogether, these results suggest that NKCC2 does not participate in cell volume recovery and therefore, NKCC1 and NKCC2 are functionally different Na(+)K(+)2Cl(−) co-transporters.
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spelling pubmed-52093642017-01-18 Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation Singh, Richa Kursan, Shams Almiahoub, Mohamed Y. Almutairi, Mohammed M. Garzón-Muvdi, Tomás Alvarez-Leefmans, Francisco J. Di Fulvio, Mauricio Front Cell Dev Biol Cell and Developmental Biology Na(+)K(+)2Cl(−) co-transporters (NKCCs) effect the electroneutral movement of Na(+)-K(+) and 2Cl(−) ions across the plasma membrane of vertebrate cells. There are two known NKCC isoforms, NKCC1 (Slc12a2) and NKCC2 (Slc12a1). NKCC1 is a ubiquitously expressed transporter involved in cell volume regulation, Cl(−) homeostasis and epithelial salt secretion, whereas NKCC2 is abundantly expressed in kidney epithelial cells of the thick ascending loop of Henle, where it plays key roles in NaCl reabsorption and electrolyte homeostasis. Although NKCC1 and NKCC2 co-transport the same ions with identical stoichiometry, NKCC1 actively co-transports water whereas NKCC2 does not. There is growing evidence showing that NKCC2 is expressed outside the kidney, but its function in extra-renal tissues remains unknown. The present study shows molecular and functional evidence of endogenous NKCC2 expression in COS7 cells, a widely used mammalian cell model. Endogenous NKCC2 is primarily found in recycling endosomes, Golgi cisternae, Golgi-derived vesicles, and to a lesser extent in the endoplasmic reticulum. Unlike NKCC1, NKCC2 is minimally hybrid/complex N-glycosylated under basal conditions and yet it is trafficked to the plasma membrane region of hyper-osmotically challenged cells through mechanisms that require minimal complex N-glycosylation or functional Golgi cisternae. Control COS7 cells exposed to slightly hyperosmotic (~6.7%) solutions for 16 h were not shrunken, suggesting that either one or both NKCC1 and NKCC2 may participate in cell volume recovery. However, NKCC2 targeted to the plasma membrane region or transient over-expression of NKCC2 failed to rescue NKCC1 in COS7 cells where NKCC1 had been silenced. Further, COS7 cells in which NKCC1, but not NKCC2, was silenced exhibited reduced cell size compared to control cells. Altogether, these results suggest that NKCC2 does not participate in cell volume recovery and therefore, NKCC1 and NKCC2 are functionally different Na(+)K(+)2Cl(−) co-transporters. Frontiers Media S.A. 2017-01-04 /pmc/articles/PMC5209364/ /pubmed/28101499 http://dx.doi.org/10.3389/fcell.2016.00150 Text en Copyright © 2017 Singh, Kursan, Almiahoub, Almutairi, Garzón-Muvdi, Alvarez-Leefmans and Di Fulvio. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Singh, Richa
Kursan, Shams
Almiahoub, Mohamed Y.
Almutairi, Mohammed M.
Garzón-Muvdi, Tomás
Alvarez-Leefmans, Francisco J.
Di Fulvio, Mauricio
Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title_full Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title_fullStr Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title_full_unstemmed Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title_short Plasma Membrane Targeting of Endogenous NKCC2 in COS7 Cells Bypasses Functional Golgi Cisternae and Complex N-Glycosylation
title_sort plasma membrane targeting of endogenous nkcc2 in cos7 cells bypasses functional golgi cisternae and complex n-glycosylation
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209364/
https://www.ncbi.nlm.nih.gov/pubmed/28101499
http://dx.doi.org/10.3389/fcell.2016.00150
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