Toma Kishio, Otsuka Fumio, Oguni Kohei, Terasaka Tomohiro, Komatsubara Motoshi, Tsukamoto-Yamauchi Naoko, Inagaki Kenichi, Makino Hirofumi
Department of Medicine and Clinical Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Peptides. 2016 Feb;76:96-101. doi: 10.1016/j.peptides.2016.01.011. Epub 2016 Jan 15.
The effects of somatostatin analogs and roles of BMP-6 in the regulation of luteinizing hormone (LH) secretion were investigated using mouse gonadotrope LβT2 cells. LH mRNA expression and LH secretion induced by GnRH were suppressed by treatments with somatostatin analogs, including octreotide and pasireotide, in LβT2 cells. Of note, the inhibitory effects of somatostatin analogs on LH secretion were enhanced by the action of BMP-6. BMP-6 increased the expression levels of somatostatin receptor (SSTR)5, suggesting that BMP-6 upregulates SSTR activity that leads to reduction of GnRH-induced LH secretion. In addition, GnRH-induced phosphorylation of MAPKs including ERK, but not P38 or SAPK, was suppressed by pasireotide in the presence of BMP-6. Given that each inhibitor of ERK, JNK or P38 signaling suppressed GnRH-induced LH transcription, MAPKs are individually involved in the induction of LH production by LβT2 cells. Somatostatin analogs also impaired BMP-6-induced Smad1/5/8 phosphorylation by suppressing BMPRs and augmenting Smad6/7 expression. Collectively, the results indicate that somatostatin analogs have dual effects on the modulation of GnRH-induced MAPK signaling and BMP activity. The pituitary BMP system may play a regulatory role in GnRH-induced LH secretion by tuning the responsiveness to somatostatin analogs in gonadotrope cells.
利用小鼠促性腺激素细胞LβT2研究了生长抑素类似物的作用以及骨形态发生蛋白-6(BMP-6)在调节促黄体生成素(LH)分泌中的作用。在LβT2细胞中,用包括奥曲肽和帕瑞肽在内的生长抑素类似物处理可抑制GnRH诱导的LH mRNA表达和LH分泌。值得注意的是,BMP-6的作用增强了生长抑素类似物对LH分泌的抑制作用。BMP-6增加了生长抑素受体(SSTR)5的表达水平,这表明BMP-6上调了SSTR活性,导致GnRH诱导的LH分泌减少。此外,在BMP-6存在的情况下,帕瑞肽可抑制GnRH诱导的包括ERK在内的丝裂原活化蛋白激酶(MAPK)的磷酸化,但不抑制P38或应激激活蛋白激酶(SAPK)。鉴于ERK、JNK或P38信号通路的每种抑制剂均抑制GnRH诱导的LH转录,MAPK分别参与LβT2细胞诱导LH产生的过程。生长抑素类似物还通过抑制骨形态发生蛋白受体(BMPRs)并增强Smad6/7表达来损害BMP-6诱导的Smad1/5/8磷酸化。总体而言,结果表明生长抑素类似物对GnRH诱导的MAPK信号传导和BMP活性的调节具有双重作用。垂体BMP系统可能通过调节促性腺激素细胞对生长抑素类似物的反应性,在GnRH诱导的LH分泌中发挥调节作用。