Philyppov Igor B, Sotkis Ganna V, Sharopov Bizhan R, Danshyna Anastasiia O, Yelyashov Semen I, Naidenov Valeri G, Lyubanova Olga P, Shuba Yaroslav M
Bogomoletz Institute of Physiology of the National Academy of Sciences of Ukraine, Kyiv, Ukraine.
BBA Adv. 2022 Dec 20;3:100069. doi: 10.1016/j.bbadva.2022.100069. eCollection 2023.
Tunica dartos smooth muscle (TDSM) lies beneath the scrotal skin, and its contraction leads to scrotum wrinkling upon cooling. However, neither the nature of TDSM cold-sensitivity nor the underlying molecular sensors are well understood. Here we have investigated the role of cold/menthol-sensitive TRPM8 channel in TDSM temperature-dependent contractility. The contraction of isolated male rat TDSM strips was studied by tensiometry. TRPM8 expression was assayed by RT-PCR and fluorescence immunochemistry. Isolated TDSM strips responded to cooling from 33 °C to 20 °C by enhancement of basal tension, and increase of the amplitude and duration of electric field stimulated (EFS) contractions. The effects of cold on basal tension, but not on EFS-contractions, could be 80% inhibited by TRPM8 blockers, capsazepine and BCTC [N-(4‑tert-butylphenyl)-4-(3-chloropyridin-2-yl)piperazine-1-carboxamide], and could be partially mimicked by menthol. RT-PCR and immunolabeling showed TRPM8 mRNA and protein expression in TDSM cells with protein labelling being predominantly localized to intracellular compartments. Chemical castration of male rats consequent to the treatment with androgen receptor blocker, flutamide, led to the abrogation of cold effects on TDSM basal tension, but not on EFS-contractions, and to the disappearance of TRPM8 protein expression. We conclude that TRPM8 is involved in the maintenance of basal cold-induced TDSM tonus, but not in sympathetic nerve-mediated contractility, by acting as endoplasmic reticulum Ca release channel whose expression in TDSM cells requires the presence of a functional androgen receptor. Thus, TRPM8 plays a crucial role in scrotal thermoregulation which is important for maintaining normal spermatogenesis and male fertility.
肉膜平滑肌(TDSM)位于阴囊皮肤下方,其收缩会导致阴囊在冷却时起皱。然而,TDSM冷敏感性的本质以及潜在的分子传感器都尚未得到充分了解。在此,我们研究了冷/薄荷醇敏感的TRPM8通道在TDSM温度依赖性收缩中的作用。通过张力测定法研究了分离的雄性大鼠TDSM条带的收缩情况。通过RT-PCR和荧光免疫化学法检测TRPM8的表达。分离的TDSM条带在从33°C冷却至20°C时,基础张力增强,电场刺激(EFS)收缩的幅度和持续时间增加。TRPM8阻滞剂辣椒素和BCTC [N-(4-叔丁基苯基)-4-(3-氯吡啶-2-基)哌嗪-1-甲酰胺]可抑制冷对基础张力的影响,但不影响EFS收缩,且薄荷醇可部分模拟这种影响。RT-PCR和免疫标记显示TDSM细胞中有TRPM8 mRNA和蛋白表达,蛋白标记主要定位于细胞内区室。用雄激素受体阻滞剂氟他胺治疗雄性大鼠导致化学去势,这使得冷对TDSM基础张力的影响消失,但不影响EFS收缩,并且TRPM8蛋白表达也消失。我们得出结论,TRPM8作为内质网钙释放通道参与基础冷诱导的TDSM张力的维持,但不参与交感神经介导的收缩,其在TDSM细胞中的表达需要功能性雄激素受体的存在。因此,TRPM8在阴囊温度调节中起关键作用,这对维持正常精子发生和男性生育能力很重要。