Boldyrev O I, Sotkis H V, Kuliieva Ie M, Vladymyrova I A, Filippov I B, Skryma R, Prevars'ka N, Shuba Ia M
Fiziol Zh (1994). 2009;55(5):17-27.
By means of real-time RT-PCR and immunofluorscent staining combined with confocal microscopy we show for the first time the expression ofmRNA and protein ofthe cold/menthol-sensitive cationic channel, TRPM8, in the smooth muscle cells (SMC) from the epididimal and prostatic portions of the rat vas deferens. Expression of TRPM8 mRNA correlated with the expression ofmRNA for androgen receptor (AR): orchidectomy of the animals resulted in the enhancement of the expression of both mRNAs, which likely reflects specific for the vas deferens compensatory response to the decreasing levels of circulating androgens. TRPM8 protein in the SMC from both parts of the vas deferens primarily localized outside the plasma membrane (PM), however, in the SMC from prostatic portion we observed higher TRPM8 protein targeting specifically the endoplasmic reticulum and PM, where it can form functional cold/menthol-sensitive cationic channel capable of modulating contractile activity of the smooth muscle.
通过实时逆转录聚合酶链反应(RT-PCR)以及免疫荧光染色结合共聚焦显微镜技术,我们首次展示了冷/薄荷醇敏感阳离子通道TRPM8的mRNA和蛋白质在大鼠输精管附睾段和前列腺段平滑肌细胞(SMC)中的表达。TRPM8 mRNA的表达与雄激素受体(AR)mRNA的表达相关:动物去势导致两种mRNA表达增强,这可能反映了输精管对循环雄激素水平降低的特异性代偿反应。输精管两部分的SMC中的TRPM8蛋白主要定位于质膜(PM)外,然而,在前列腺段的SMC中,我们观察到更高水平的TRPM8蛋白特异性靶向内质网和质膜,在那里它可以形成能够调节平滑肌收缩活性的功能性冷/薄荷醇敏感阳离子通道。