Laboratory of Veterinary Physiology, Faculty of Veterinary Medicine, Okayama University of Science, Ehime 794-8555, Japan.
Endocr J. 2022 Oct 28;69(10):1193-1200. doi: 10.1507/endocrj.EJ22-0095. Epub 2022 May 19.
Recently, we reported that gonadotropin-releasing hormone (GnRH) stimulates annexin A1 (Anxa1) and A5 (Anxa5) mRNA expression through the GnRH-receptor-mitogen-activated protein kinase cascade in LβT2 cells. As LβT2 cells respond to activin, we examined the effect of activin A on Anxa1 and a5 expression in LβT2 cells. Activin A (0.4 and 4 ng/mL) treatment decreased Anxa5 mRNA levels in a dose-dependent manner, but did not affect Anxa1 mRNA levels at concentrations up to 40 ng/mL. After activin A treatment (4 ng/mL), Anxa5 mRNA levels significantly decreased at 6 h, gradually declined until 24 h, and remained low until 48 h, whereas Anxa1 mRNA levels did not significantly change following treatment. Pretreatment with activin A for 24 h increased GnRH agonist (GnRHa)-induced Anxa1 increase by approximately 7-fold compared with GnRHa stimulation alone, but Anxa5 was not affected. As previously reported, these activin A treatments increased gonadotropin β subunit and GnRH receptor mRNA levels and slightly decreased common α-glycoprotein subunit mRNA levels. Furthermore, we examined the effect of activin A on Nr4a3, which is repressed by ANXA5 and which reduces Fshb expression, and found that activin A augmented Nr4a3 expression and slightly decreased the GnRHa-induced increase in Nr4a3. These results suggest that in gonadotrope cells, the mechanism regulating Anxa1 and a5 expression is differentially coupled with activin A signal transduction. Activin A suppresses Anxa5 expression under increased Nr4a3 expression, whereas activin A and GnRH synergistically stimulate Anxa1 expression. These GnRH-inducible annexins may have different specific functions in gonadotropes.
最近,我们报道了促性腺激素释放激素(GnRH)通过 GnRH 受体-丝裂原活化蛋白激酶级联刺激 LβT2 细胞中 Annexin A1(Anxa1)和 A5(Anxa5)mRNA 的表达。由于 LβT2 细胞对激活素有反应,我们研究了激活素 A 对 LβT2 细胞中 Anxa1 和 a5 表达的影响。激活素 A(0.4 和 4ng/mL)处理以剂量依赖性方式降低 Anxa5 mRNA 水平,但在高达 40ng/mL 的浓度下不影响 Anxa1 mRNA 水平。激活素 A 处理(4ng/mL)后,Anxa5 mRNA 水平在 6 小时显著降低,逐渐下降至 24 小时,并持续至 48 小时保持低水平,而 Anxa1 mRNA 水平在处理后没有明显变化。与单独用 GnRHa 刺激相比,激活素 A 预处理 24 小时可使 GnRHa 诱导的 Anxa1 增加约 7 倍,但对 Anxa5 没有影响。如前所述,这些激活素 A 处理增加了促性腺激素β亚基和 GnRH 受体 mRNA 水平,并略微降低了共同的α-糖蛋白亚基 mRNA 水平。此外,我们研究了激活素 A 对 Nr4a3 的影响,Nr4a3 受 ANXA5 抑制,减少 Fshb 表达,发现激活素 A 增强了 Nr4a3 的表达,并略微降低了 GnRHa 诱导的 Nr4a3 增加。这些结果表明,在促性腺激素细胞中,调节 Anxa1 和 a5 表达的机制与激活素 A 信号转导不同偶联。激活素 A 在 Nr4a3 表达增加的情况下抑制 Anxa5 表达,而激活素 A 和 GnRH 协同刺激 Anxa1 表达。这些 GnRH 诱导的 Annexin 可能在促性腺激素细胞中有不同的特定功能。