TY - JOUR
T1 - Plasma membrane targeting of endogenous NKCC2 in COS7 cells bypasses functional golgi cisternae and complex N-glycosylation
AU - Singh, Richa
AU - Kursan, Shams
AU - Almiahoub, Mohamed Y.
AU - Almutairi, Mohammed M.
AU - Garzón-Muvdi, Tomás
AU - Alvarez-Leefmans, Francisco J.
AU - Di Fulvio, Mauricio
N1 - Funding Information:
Scholarship from King Saud University (Saudi Arabia) supported MMA. We are grateful to Dr. Gary Shull for providing NKCC1 mice for our studies, and to Dr. Pablo Ortiz for its comments to the manuscript and for providing the anti-NKCC2 antibodies used in this study. This work was partially supported by funding from the Boonshoft School of Medicine, Wright State University, Emerging Science and Seed Grant Programs 229113 to MD and 226191 to FJA-L, as well as NIH-NIDS Grant NS-29227 to FJA-L.
Publisher Copyright:
© 2017 Singh, Kursan, Almiahoub, Almutairi, Garzón-Muvdi, Alvarez-Leefmans and Di Fulvio.
PY - 2017/1/4
Y1 - 2017/1/4
N2 - 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.
AB - 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.
KW - COS7
KW - Cell volume
KW - Golgi
KW - N-glycosylation
KW - NKCC2A
UR - http://www.scopus.com/inward/record.url?scp=85019223964&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85019223964&partnerID=8YFLogxK
U2 - 10.3389/fcell.2016.00150
DO - 10.3389/fcell.2016.00150
M3 - Article
C2 - 28101499
AN - SCOPUS:85019223964
SN - 2296-634X
VL - 4
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
IS - JAN
M1 - 150
ER -