Literature DB >> 19878209

The role of TASK1 in aldosterone production and its expression in normal adrenal and aldosterone-producing adenomas.

Edson F Nogueira1, Daniel Gerry, Franco Mantero, Barbara Mariniello, William E Rainey.   

Abstract

OBJECTIVES: Aldosterone production in the adrenal glomerulosa is mainly regulated by angiotensin II and K+. Adrenal glomerulosa cells are uniquely sensitive to extracellular K+. Genetic deletion of subunits of K+-selective leak-channels (KCNK), TASK1 and/or TASK3, in mice generates animals with hyperaldosteronism and histological changes in the adrenal cortex. Herein, we studied the expression of TASK1 in human adrenocortical cells, as well as its role in aldosterone production in H295R cells.
DESIGN: TASK1 expression was investigated by comparative microarray analysis of aldosterone-producing adenomas (APA) and normal adrenals (NAs). The effects of TASK1 knockdown by siRNA transfection were investigated in H295R cells. Fluo-4 fluorescent measurements of intracellular Ca2+ and pharmacological inhibition of Ca2+ -dependent calmodulin kinases (CaMK) were performed to better define the effects of TASK1 on Ca2+ signalling pathways.
RESULTS: Microarray analysis of APA and NA showed similar expression of TASK1 between these two groups. However, in APA, NA and H295R cells the expression of TASK1 was predominant when compared with other KCNK family members. Knockdown of TASK1 (with siRNA) induced the expression of steroidogenic acute regulatory (StAR) protein and aldosterone synthase (CYP11B2), and also stimulated pregnenolone and aldosterone production. Cells transfected with siTASK1 had increased intracellular Ca2+, leading to activation of CaMK and increased expression of CYP11B2.
CONCLUSIONS: Our study reveals the predominant expression of TASK1 over other KCNK family genes in the human adrenal cortex. Herein, we also described the role of TASK1 in the regulation of human aldosterone production through regulation of intracellular Ca2+ and CaMK signalling pathways.

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Year:  2009        PMID: 19878209      PMCID: PMC4158746          DOI: 10.1111/j.1365-2265.2009.03738.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  43 in total

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Journal:  Lancet       Date:  2008-06-07       Impact factor: 79.321

Review 2.  Aldosterone antagonists in hypertension and heart failure.

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3.  Primary hyperaldosteronism in essential hypertensives: prevalence, biochemical profile, and molecular biology.

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4.  TASK (TWIK-related acid-sensitive K+ channel) is expressed in glomerulosa cells of rat adrenal cortex and inhibited by angiotensin II.

Authors:  G Czirják; T Fischer; A Spät; F Lesage; P Enyedi
Journal:  Mol Endocrinol       Date:  2000-06

5.  Both TASK-3 and TREK-1 two-pore loop K channels are expressed in H295R cells and modulate their membrane potential and aldosterone secretion.

Authors:  Tanja Brenner; Kevin M O'Shaughnessy
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-10-14       Impact factor: 4.310

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7.  [Prevalence of primary aldosteronism in hypertensive patients and its effect on the heart].

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8.  Role of angiotensin II-induced rapid response genes in the regulation of enzymes needed for aldosterone synthesis.

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Journal:  J Mol Endocrinol       Date:  2009-01-21       Impact factor: 5.098

Review 9.  Primary aldosteronism: an update on screening, diagnosis and treatment.

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10.  TASK channel deletion in mice causes primary hyperaldosteronism.

Authors:  Lucinda A Davies; Changlong Hu; Nick A Guagliardo; Neil Sen; Xiangdong Chen; Edmund M Talley; Robert M Carey; Douglas A Bayliss; Paula Q Barrett
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205

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Journal:  Mol Cell Endocrinol       Date:  2015-09-12       Impact factor: 4.102

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6.  Channels and pumps in aldosterone-producing adenomas.

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7.  Adrenal Tissue-Specific Deletion of TASK Channels Causes Aldosterone-Driven Angiotensin II-Independent Hypertension.

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Review 8.  Human adrenocortical carcinoma cell lines.

Authors:  Tao Wang; William E Rainey
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Review 10.  Role of KCNJ5 in familial and sporadic primary aldosteronism.

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