Papadopoulos Dimitrios, Dietze Raimund, Shihan Mazen, Kirch Ulrike, Scheiner-Bobis Georgios
Institut für Veterinär-Physiologie und -Biochemie, Fachbereich Veterinärmedizin, Justus-Liebig-Universität Giessen, Giessen, Germany.
PLoS One. 2016 Mar 3;11(3):e0150143. doi: 10.1371/journal.pone.0150143. eCollection 2016.
Dehydroepiandrosterone sulfate (DHEAS) is a circulating sulfated steroid considered to be a pro-androgen in mammalian physiology. Here we show that at a physiological concentration (1 μM), DHEAS induces the phosphorylation of the kinase Erk1/2 and of the transcription factors CREB and ATF-1 in the murine Sertoli cell line TM4. This signaling cascade stimulates the expression of the tight junction (TJ) proteins claudin-3 and claudin-5. As a consequence of the increased expression, tight junction connections between neighboring Sertoli cells are augmented, as demonstrated by measurements of transepithelial resistance. Phosphorylation of Erk1/2, CREB, or ATF-1 is not affected by the presence of the steroid sulfatase inhibitor STX64. Erk1/2 phosphorylation was not observed when dehydroepiandrosterone (DHEA) was used instead of DHEAS. Abrogation of androgen receptor (AR) expression by siRNA did not affect DHEAS-stimulated Erk1/2 phosphorylation, nor did it change DHEAS-induced stimulation of claudin-3 and claudin-5 expression. All of the above indicate that desulfation and conversion of DHEAS into a different steroid hormone is not required to trigger the DHEAS-induced signaling cascade. All activating effects of DHEAS, however, are abolished when the expression of the G-protein Gnα11 is suppressed by siRNA, including claudin-3 and -5 expression and TJ formation between neighboring Sertoli cells as indicated by reduced transepithelial resistance. Taken together, these results are consistent with the effects of DHEAS being mediated through a membrane-bound G-protein-coupled receptor interacting with Gnα11 in a signaling pathway that resembles the non-classical signaling pathways of steroid hormones. Considering the fact that DHEAS is produced in reproductive organs, these findings also suggest that DHEAS, by acting as an autonomous steroid hormone and influencing the formation and dynamics of the TJ at the blood-testis barrier, might play a crucial role for the regulation and maintenance of male fertility.
硫酸脱氢表雄酮(DHEAS)是一种循环中的硫酸化类固醇,在哺乳动物生理学中被认为是一种雄激素前体。在此我们表明,在生理浓度(1μM)下,DHEAS可诱导小鼠支持细胞系TM4中激酶Erk1/2以及转录因子CREB和ATF-1的磷酸化。这一信号级联反应刺激紧密连接(TJ)蛋白claudin-3和claudin-5的表达。由于表达增加,相邻支持细胞之间的紧密连接连接增强,这通过跨上皮电阻的测量得以证明。Erk1/2、CREB或ATF-1的磷酸化不受类固醇硫酸酯酶抑制剂STX64存在的影响。当使用脱氢表雄酮(DHEA)而非DHEAS时,未观察到Erk1/2磷酸化。通过小干扰RNA(siRNA)消除雄激素受体(AR)表达并不影响DHEAS刺激的Erk1/2磷酸化,也未改变DHEAS诱导的claudin-3和claudin-5表达的刺激。上述所有结果表明,DHEAS触发诱导信号级联反应无需进行去硫酸化并转化为另一种类固醇激素。然而,当siRNA抑制G蛋白Gnα11的表达时,DHEAS的所有激活作用均被消除,包括claudin-3和-5的表达以及相邻支持细胞之间紧密连接的形成,这通过降低的跨上皮电阻得以表明。综上所述,这些结果与DHEAS的作用是通过膜结合的G蛋白偶联受体介导的一致,该受体在类似于类固醇激素非经典信号通路的信号通路中与Gnα11相互作用。鉴于DHEAS在生殖器官中产生,这些发现还表明,DHEAS作为一种自主的类固醇激素,通过影响血睾屏障处紧密连接的形成和动态变化,可能在男性生育力的调节和维持中发挥关键作用。