Lang F, Paulmichl M
Department for Physiology, University of Tübingen, Germany.
Kidney Int. 1995 Oct;48(4):1200-5. doi: 10.1038/ki.1995.403.
The MDCK cell has proven to be a useful model cell line for the study of properties and regulation of renal epithelial ion channels. Patch clamp studies disclosed the existence of several K+ channels and of a Cl- channel, and their regulation by hormones, cell volume, trace elements and drugs. Most hormones affect K+ channels at least in part by increasing cytosolic Ca2+. However, indirect evidence points to additional mechanisms contributing to K+ channel activation. Cell swelling activates both K+ channels and unselective anion channels. ICln, a protein cloned from MDCK cells, is either a Cl- channel or a regulator of thereof. ICln is up-regulated by cellular acidification and is crucial for rapid regulatory cell volume decrease.
已证明MDCK细胞是研究肾上皮离子通道特性和调节的有用模型细胞系。膜片钳研究揭示了几种钾离子通道和一种氯离子通道的存在,以及它们受激素、细胞体积、微量元素和药物的调节。大多数激素至少部分地通过增加胞质钙离子来影响钾离子通道。然而,间接证据表明还有其他机制参与钾离子通道的激活。细胞肿胀可激活钾离子通道和非选择性阴离子通道。ICln是一种从MDCK细胞中克隆的蛋白质,它要么是一种氯离子通道,要么是其调节剂。ICln在细胞酸化时上调,对快速调节性细胞体积减小至关重要。