Literature DB >> 11875121

TASK-3 dominates the background potassium conductance in rat adrenal glomerulosa cells.

Gábor Czirják1, Péter Enyedi.   

Abstract

In a preceding study we showed that the highly negative resting membrane potential of rat adrenal glomerulosa cells is related to background potassium channel(s), which belong to the two-pore domain channel family. TWIK-related acid-sensitive K+ channel (TASK-1) expression was found in glomerulosa tissue, and the currents elicited by injection of glomerulosa mRNA (I(glom)) or TASK-1 cRNA (I(TASK-1)) showed remarkable similarity in Xenopus laevis oocytes. However, based on the different sensitivity of these currents to acidification, we concluded that TASK-1 may be responsible for a maximum of 25% of the weakly pH-dependent glomerulosa background K+ current. Here we demonstrate that TASK-3, a close relative of TASK-1, is expressed abundantly in glomerulosa cells. Northern blot detected TASK-3 message in adrenal glomerulosa, but not in other tissues. Quantitative RT-PCR experiments indicated even higher mRNA expression of TASK-3 than TASK-1 in glomerulosa tissue. Similarly to the glomerulosa background current, the current expressed by injection of TASK-3 cRNA (I(TASK-3)) was less acid-sensitive than I(TASK-1). Ruthenium red in the micromolar range inhibited I(glom) and I(TASK-3), but not I(TASK-1). Like I(TASK-1), I(TASK-3) was inhibited by stimulation of AT1a angiotensin II receptor coexpressed with the potassium channel. The high level of expression and its pharmacological properties suggest that TASK-3 dominates the resting potassium conductance of glomerulosa cells.

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Year:  2002        PMID: 11875121     DOI: 10.1210/mend.16.3.0788

Source DB:  PubMed          Journal:  Mol Endocrinol        ISSN: 0888-8809


  47 in total

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Review 2.  Special features of mitochondrial Ca²⁺ signalling in adrenal glomerulosa cells.

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Review 3.  Minireview: aldosterone biosynthesis: electrically gated for our protection.

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4.  Breathing Stimulant Compounds Inhibit TASK-3 Potassium Channel Function Likely by Binding at a Common Site in the Channel Pore.

Authors:  Rikki H Chokshi; Aaron T Larsen; Brijesh Bhayana; Joseph F Cotten
Journal:  Mol Pharmacol       Date:  2015-08-12       Impact factor: 4.436

5.  Functional TASK-3-Like Channels in Mitochondria of Aldosterone-Producing Zona Glomerulosa Cells.

Authors:  Junlan Yao; David McHedlishvili; William E McIntire; Nick A Guagliardo; Alev Erisir; Craig A Coburn; Vincent P Santarelli; Douglas A Bayliss; Paula Q Barrett
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6.  Biophysical and pharmacological characteristics of native two-pore domain TASK channels in rat adrenal glomerulosa cells.

Authors:  David P Lotshaw
Journal:  J Membr Biol       Date:  2006-06-22       Impact factor: 1.843

7.  Mitochondrial expression of the two-pore domain TASK-3 channels in malignantly transformed and non-malignant human cells.

Authors:  Zoltán Rusznák; Gábor Bakondi; Lívia Kosztka; Krisztina Pocsai; Beatrix Dienes; János Fodor; Andrea Telek; Mónika Gönczi; Géza Szucs; László Csernoch
Journal:  Virchows Arch       Date:  2007-12-20       Impact factor: 4.064

8.  Effects of divalent cations and spermine on the K+ channel TASK-3 and on the outward current in thalamic neurons.

Authors:  Boris Musset; Sven G Meuth; Gong Xin Liu; Christian Derst; Sven Wegner; Hans-Christian Pape; Thomas Budde; Regina Preisig-Müller; Jürgen Daut
Journal:  J Physiol       Date:  2006-05-01       Impact factor: 5.182

9.  Intracellular traffic of the K+ channels TASK-1 and TASK-3: role of N- and C-terminal sorting signals and interaction with 14-3-3 proteins.

Authors:  Marylou Zuzarte; Katja Heusser; Vijay Renigunta; Günter Schlichthörl; Susanne Rinné; Erhard Wischmeyer; Jürgen Daut; Blanche Schwappach; Regina Preisig-Müller
Journal:  J Physiol       Date:  2009-01-12       Impact factor: 5.182

10.  Variations in the potassium channel genes KCNK3 and KCNK9 in relation to blood pressure and aldosterone production: an exploratory study.

Authors:  Jeesun Jung; Paula Q Barrett; George J Eckert; Howard J Edenberg; Xiaoling Xuei; Wanzhu Tu; J Howard Pratt
Journal:  J Clin Endocrinol Metab       Date:  2012-08-14       Impact factor: 5.958

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