TY - JOUR
T1 - Pendrin localizes to the adrenal medulla and modulates catecholamine release
AU - Lazo-Fernandez, Yoskaly
AU - Aguilera, Greti
AU - Pham, Truyen D.
AU - Park, Annie Y.
AU - Beierwaltes, William H.
AU - Sutliff, Roy L.
AU - Verlander, Jill W.
AU - Pacak, Karel
AU - Osunkoya, Adeboye O.
AU - Ellis, Carla LaShannon
AU - Kim, Young Hee
AU - Shipley, Gregory L.
AU - Wynne, Brandi M.
AU - Hoover, Robert S.
AU - Sen, Shurjo K.
AU - Plotsky, Paul M.
AU - Wall, Susan M.
N1 - Publisher Copyright:
© 2015 The American Physiological Society.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2015/9/15
Y1 - 2015/9/15
N2 - Pendrin (Slc26a4) is a Cl–/HCO3– exchanger expressed in renal intercalated cells and mediates renal Cl– absorption. With pendrin gene ablation, blood pressure and vascular volume fall, which increases plasma renin concentration. However, serum aldosterone does not significantly increase in pendrin-null mice, suggesting that pendrin regulates adrenal zona glomerulosa aldosterone production. Therefore, we examined pendrin expression in the adrenal gland using PCR, immunoblots, and immunohistochemistry. Pendrin protein was detected in adrenal lysates from wild-type but not pendrin-null mice. However, immunohistochemistry and qPCR of microdissected adrenal zones showed that pendrin was expressed in the adrenal medulla, rather than in cortex. Within the adrenal medulla, pendrin localizes to both epinephrine- and norepinephrine-producing chromaffin cells. Therefore, we examined plasma catecholamine concentration and blood pressure in wild-type and pendrin-null mice under basal conditions and then after 5 and 20 min of immobilization stress. Under basal conditions, blood pressure was lower in the mutant than in the wild-type mice, although epinephrine and norepinephrine concentrations were similar. Catecholamine concentration and blood pressure increased markedly in both groups with stress. With 20 min of immobilization stress, epinephrine and norepinephrine concentrations increased more in pendrin-null than in wild-type mice, although stress produced a similar increase in blood pressure in both groups. We conclude that pendrin is expressed in the adrenal medulla, where it blunts stress-induced catecholamine release.
AB - Pendrin (Slc26a4) is a Cl–/HCO3– exchanger expressed in renal intercalated cells and mediates renal Cl– absorption. With pendrin gene ablation, blood pressure and vascular volume fall, which increases plasma renin concentration. However, serum aldosterone does not significantly increase in pendrin-null mice, suggesting that pendrin regulates adrenal zona glomerulosa aldosterone production. Therefore, we examined pendrin expression in the adrenal gland using PCR, immunoblots, and immunohistochemistry. Pendrin protein was detected in adrenal lysates from wild-type but not pendrin-null mice. However, immunohistochemistry and qPCR of microdissected adrenal zones showed that pendrin was expressed in the adrenal medulla, rather than in cortex. Within the adrenal medulla, pendrin localizes to both epinephrine- and norepinephrine-producing chromaffin cells. Therefore, we examined plasma catecholamine concentration and blood pressure in wild-type and pendrin-null mice under basal conditions and then after 5 and 20 min of immobilization stress. Under basal conditions, blood pressure was lower in the mutant than in the wild-type mice, although epinephrine and norepinephrine concentrations were similar. Catecholamine concentration and blood pressure increased markedly in both groups with stress. With 20 min of immobilization stress, epinephrine and norepinephrine concentrations increased more in pendrin-null than in wild-type mice, although stress produced a similar increase in blood pressure in both groups. We conclude that pendrin is expressed in the adrenal medulla, where it blunts stress-induced catecholamine release.
KW - Chloride
KW - Dopamine
KW - Epinephrine
KW - Norepinephrine
KW - Pendrin
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U2 - 10.1152/ajpendo.00035.2015
DO - 10.1152/ajpendo.00035.2015
M3 - Article
C2 - 26173457
AN - SCOPUS:84941695426
VL - 309
SP - E534-E545
JO - American Journal of Physiology
JF - American Journal of Physiology
SN - 0193-1849
IS - 6
ER -