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胆碱能诱导培养的人汗腺导管细胞中振荡性跨上皮短路电流

Cholinergic-induced oscillating transepithelial short-circuit current in cultured human sweat duct cells.

作者信息

Pedersen P S

机构信息

University Department of Pediatrics, Rigshopitalet, Copenhagen, Denmark.

出版信息

Acta Physiol Scand. 1990 Mar;138(3):359-68. doi: 10.1111/j.1748-1716.1990.tb08858.x.

DOI:10.1111/j.1748-1716.1990.tb08858.x
PMID:2183541
Abstract

Human sweat duct cells in primary culture were investigated by voltage-clamp technique. Stimulation with the muscarinic agonist, metacholine (MCh), produced an abrupt transient rise followed by sustained regular oscillations in the transepithelial short-circuit current (Iscc), which in these cells is carried by a mucosal amiloride-sensitive Na+ influx, secondary to a Ca2(+)-activated, voltage-dependent, large K+ shunt across the serosal membrane. The time of latency, the initial transient phase, and the sustained oscillating phase of the MCh-induced Iscc response were demonstrated to be differently affected by changes in temperature, agonist concentration and external Ca2+ supply. From these results a model is proposed for the MCh-induced signal transduction in cultured sweat duct cells, involving a primary intracellular oscillatory Ca2+ mobilization, activated by IPP, sustained by a temperature-regulated external Ca2+ supply, and counter-regulated by cytosolic Ca2+.

摘要

采用电压钳技术对原代培养的人汗腺导管细胞进行了研究。用毒蕈碱激动剂乙酰甲胆碱(MCh)刺激后,跨上皮短路电流(Iscc)出现突然的瞬时升高,随后是持续的规则振荡,在这些细胞中,该电流由黏膜阿米洛利敏感的Na +内流携带,继发于Ca2(+)激活的、电压依赖性的、穿过浆膜的大K +分流。结果表明,MCh诱导的Iscc反应的潜伏期、初始瞬态阶段和持续振荡阶段受温度、激动剂浓度和细胞外Ca2 +供应变化的影响不同。根据这些结果,提出了一个在培养的汗腺导管细胞中MCh诱导的信号转导模型,该模型涉及由IPP激活的初级细胞内振荡性Ca2 +动员,由温度调节的细胞外Ca2 +供应维持,并由胞质Ca2 +进行反向调节。

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引用本文的文献

1
Separate agonist-specific oscillatory mechanisms in cultured human sweat duct cells.培养的人汗腺导管细胞中不同激动剂特异性振荡机制。
J Physiol. 1991 Feb;433:549-59. doi: 10.1113/jphysiol.1991.sp018443.
2
Stimulus-secretion coupling: cytoplasmic calcium signals and the control of ion channels in exocrine acinar cells.刺激-分泌偶联:外分泌腺泡细胞中的细胞质钙信号与离子通道的调控
J Physiol. 1992 Mar;448:1-51. doi: 10.1113/jphysiol.1992.sp019028.