Native ciliary epithelial cells from the ciliary epithelium of the '/> Antisense to MDR1 mRNA reduces P-glycoprotein expression swelling-activated Cl− current and volume regulation in bovine ciliary epithelial cells
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Antisense to MDR1 mRNA reduces P-glycoprotein expression swelling-activated Cl− current and volume regulation in bovine ciliary epithelial cells

机译:对MDR1 mRNA的反义降低了牛睫状上皮细胞中的P-糖蛋白表达溶胀激活的Cl-电流和体积调节

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摘要

class="enumerated" style="list-style-type:decimal">Native ciliary epithelial cells from the ciliary epithelium of the eye exhibit anti-P-glycoprotein (P-gp) immunofluorescence.We have used an antisense ‘knock-down’ approach to investigate the relationship between P-gp and the volume-activated chloride current (ICl,swell) and its role in volume regulation.An antisense oligonucleotide to the human multidrug resistance (MDR1) gene, taken up by the cells in a dose-dependent manner, reduced P-gp immunofluorescence, inhibited ICl,swell and significantly increased the latency of activation of ICl,swell.Increasing the hypotonic stress did not result in an increased activation of ICl,swell. MDR1 antisense ‘knock-down’ also reduced the ability of the cells to volume regulate following a hypotonic challenge.These cells are known to express at least two volume-activated chloride channels, and the data suggest that P-gp is involved in the activation pathway of a subset of channels that contribute to whole-cell ICl,swell and participate in volume regulation.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 来自眼睫状上皮的天然睫状上皮细胞显示抗P-糖蛋白(P-gp)免疫荧光。 我们使用了一种反义“敲除”方法来研究P-gp之间的关系 人多药抗性(MDR1)基因的反义寡核苷酸,细胞以剂量依赖性方式吸收,降低P-gp免疫荧光,抑制ICl溶胀并显着增加ICl溶胀激活的潜伏期。 增加低渗应激并不会导致ICl溶胀激活增加。 MDR1反义“敲低”还降低了低渗刺激后细胞调节体积的能力。 已知这些细胞表达至少两个体积激活的氯离子通道,数据表明P -gp参与了一个通道子集的激活途径,该通道子对全细胞ICl起作用,膨胀并参与体积调节。

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