Muscarinic Receptors Control K+ Secretion in Inner Ear Strial Marginal Cells

Muscarinic Receptors Control K+ Secretion in Inner Ear Strial Marginal Cells K+ secretion in strial marginal cells (SMC) of stria vascularis (SV) is stimulated by β1-adrenergic receptors. The aim of the present study was to determine, whether SMC from the gerbil inner ear contain muscarinic receptors that inhibit K+ secretion. Receptors were identified with pharmacological tools in functional studies where K+ secretion was monitored as transepithelial current (I sc ). The cytosolic Ca2+ concentration ([Ca2+]i) was measured as fluo-4 fluorescence and cAMP production with a colorimetric immunoassay. Further, receptors were identified in SV as transcripts by cloning and sequencing of reverse-transcriptase polymerase chain reaction (RT-PCR) products. The cholinergic receptor agonist carbachol (CCh) caused a transient increase in [Ca2+]i with a half-maximal concentration value (EC 50) of (5 ± 6) × 10−6 m (n= 29) and a decrease in basal and stimulated cAMP production. Apical CCh had no effect on I sc but basolateral CCh caused a transient increase in I sc with an EC 50 of (3 ± 1) × 10−6 m and a sustained decrease of I sc with an EC 50 of (1.2 ± 0.2) × 10−5 m (n= 129). The effects of CCh on I sc and [Ca2+]i were inhibited in the presence of muscarinic antagonist 10−6 m atropine. Further, the muscarinic antagonists pirenzipine, methoctramine and para-fluoro-hexahydo-sila-defenidol (pFHHSiD) inhibited the CCh-induced transient increase of I sc with affinity constants (K DB ) of 3 × 10−8 m (pK DB = 7.54 ± 0.19, n= 17), 2 × 10−6 m (pK DB = 5.71 ± 0.26, n= 19) and 2 × 10−8 m (pK DB = 7.65 ± 0.28, n= 19) and the sustained decrease of I sc with K DB of 7 × 10−8 m (pK DB = 7.05 ± 0.09, n= 33), 6 × 10−6 m (pK DB = 5.21 ± 0.13, n= 23), 5 × 10−8 m (pK DB = 7.34 ± 0.13, n= 31), respectively. RT-PCR of total RNA isolated from SV using primers specific for the M1–M5 muscarinic receptors revealed products of the predicted sizes for the M3- and M4- but not the M1-, M2- and M5-muscarinic receptor subtypes. Sequence analysis confirmed that amplified cDNA fragments encoded gene-specific nucleotide sequences. These results suggest that K+ secretion in SMC is under the control of M3- and M4-muscarinic receptors that may be located in the basolateral membrane of strial marginal cells. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png The Journal of Membrane Biology Springer Journals

Muscarinic Receptors Control K+ Secretion in Inner Ear Strial Marginal Cells

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Publisher
Springer-Verlag
Copyright
Copyright © Inc. by 2001 Springer-Verlag New York
Subject
Life Sciences; Biochemistry, general; Human Physiology
ISSN
0022-2631
eISSN
1432-1424
D.O.I.
10.1007/s00232-001-0042-0
Publisher site
See Article on Publisher Site

Abstract

K+ secretion in strial marginal cells (SMC) of stria vascularis (SV) is stimulated by β1-adrenergic receptors. The aim of the present study was to determine, whether SMC from the gerbil inner ear contain muscarinic receptors that inhibit K+ secretion. Receptors were identified with pharmacological tools in functional studies where K+ secretion was monitored as transepithelial current (I sc ). The cytosolic Ca2+ concentration ([Ca2+]i) was measured as fluo-4 fluorescence and cAMP production with a colorimetric immunoassay. Further, receptors were identified in SV as transcripts by cloning and sequencing of reverse-transcriptase polymerase chain reaction (RT-PCR) products. The cholinergic receptor agonist carbachol (CCh) caused a transient increase in [Ca2+]i with a half-maximal concentration value (EC 50) of (5 ± 6) × 10−6 m (n= 29) and a decrease in basal and stimulated cAMP production. Apical CCh had no effect on I sc but basolateral CCh caused a transient increase in I sc with an EC 50 of (3 ± 1) × 10−6 m and a sustained decrease of I sc with an EC 50 of (1.2 ± 0.2) × 10−5 m (n= 129). The effects of CCh on I sc and [Ca2+]i were inhibited in the presence of muscarinic antagonist 10−6 m atropine. Further, the muscarinic antagonists pirenzipine, methoctramine and para-fluoro-hexahydo-sila-defenidol (pFHHSiD) inhibited the CCh-induced transient increase of I sc with affinity constants (K DB ) of 3 × 10−8 m (pK DB = 7.54 ± 0.19, n= 17), 2 × 10−6 m (pK DB = 5.71 ± 0.26, n= 19) and 2 × 10−8 m (pK DB = 7.65 ± 0.28, n= 19) and the sustained decrease of I sc with K DB of 7 × 10−8 m (pK DB = 7.05 ± 0.09, n= 33), 6 × 10−6 m (pK DB = 5.21 ± 0.13, n= 23), 5 × 10−8 m (pK DB = 7.34 ± 0.13, n= 31), respectively. RT-PCR of total RNA isolated from SV using primers specific for the M1–M5 muscarinic receptors revealed products of the predicted sizes for the M3- and M4- but not the M1-, M2- and M5-muscarinic receptor subtypes. Sequence analysis confirmed that amplified cDNA fragments encoded gene-specific nucleotide sequences. These results suggest that K+ secretion in SMC is under the control of M3- and M4-muscarinic receptors that may be located in the basolateral membrane of strial marginal cells.

Journal

The Journal of Membrane BiologySpringer Journals

Published: Aug 1, 2001

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