Wollmann Guido, Lenzner Steffen, Berger Wolfgang, Rosenthal Rita, Karl Mike O, Strauss Olaf
Institut fuer Klinische Physiologie, Charite-Universitaetsmedizin Berlin, Campus Benjamin Franklin, Germany.
Vision Res. 2006 Mar;46(5):688-98. doi: 10.1016/j.visres.2005.08.030. Epub 2005 Nov 14.
We studied electrophysiological properties of cultured retinal pigment epithelial (RPE) cells from mouse and a mouse model for Norrie disease. Wild-type RPE cells revealed the expression of ion channels known from other species: delayed-rectifier K(+) channels composed of Kv1.3 subunits, inward rectifier K(+) channels, Ca(V)1.3 L-type Ca(2+) channels and outwardly rectifying Cl(-) channels. Expression pattern and the ion channel characteristics current density, blocker sensitivity, kinetics and voltage-dependence were compared in cells from wild-type and Norrie mice. Although no significant differences were observed, our study provides a base for future studies on ion channel function and dysfunction in transgenic mouse models.
我们研究了来自小鼠的培养视网膜色素上皮(RPE)细胞以及诺里病小鼠模型的电生理特性。野生型RPE细胞显示出其他物种已知的离子通道表达:由Kv1.3亚基组成的延迟整流钾(K(+))通道、内向整流钾(K(+))通道、Ca(V)1.3 L型钙(Ca(2+))通道和外向整流氯(Cl(-))通道。比较了野生型和诺里病小鼠细胞中的表达模式以及离子通道特性,包括电流密度、阻断剂敏感性、动力学和电压依赖性。尽管未观察到显著差异,但我们的研究为未来关于转基因小鼠模型中离子通道功能和功能障碍的研究奠定了基础。