Pendrin localizes to the adrenal medulla and modulates catecholamine release

Author:

Lazo-Fernandez Yoskaly1,Aguilera Greti2,Pham Truyen D.1,Park Annie Y.1,Beierwaltes William H.3,Sutliff Roy L.14,Verlander Jill W.5,Pacak Karel6,Osunkoya Adeboye O.7,Ellis Carla L.7,Kim Young Hee1,Shipley Gregory L.8,Wynne Brandi M.1,Hoover Robert S.149,Sen Shurjo K.10,Plotsky Paul M.11,Wall Susan M.19

Affiliation:

1. Department of Medicine, Emory University School of Medicine, Atlanta, Georgia;

2. Section on Endocrine Physiology, Developmental Endocrinology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland;

3. Hypertension and Vascular Research Division, Henry Ford Hospital and Wayne State School of Medicine, Detroit, Michigan;

4. Atlanta Veterans Affairs Hospital, Atlanta, Georgia;

5. Department of Medicine, University of Florida, Gainesville, Florida;

6. Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland;

7. Department of Pathology, Emory University School of Medicine, Atlanta, Georgia;

8. Department of Integrative Biology and Pharmacology, University of Texas Medical School at Houston, Houston, Texas;

9. Department of Physiology, Emory University School of Medicine, Atlanta, Georgia

10. Cardiovascular Disease Section, and National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland;

11. Department of Psychiatry, Emory University School of Medicine, Atlanta, Georgia; and

Abstract

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.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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