Tamura Kazuhiro, Yoshie Mikihiro, Hashimoto Keisuke, Tachikawa Eiichi
Department of Endocrine and Neural Pharmacology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
J Reprod Dev. 2014;60(6):447-53. doi: 10.1262/jrd.2014-069. Epub 2014 Sep 9.
Angiogenesis in the developing corpus luteum (CL) is a prerequisite for establishment and maintenance of an early pregnancy. To explore the physiological significance of insulin-like growth factor-binding protein-7 (IGFBP7) in the developing CL, the effects of IGFBP7 on vascular endothelial growth factor (VEGFA)- and luteinizing hormone (LH)-induced in vitro tube formation were tested using isolated luteal microvascular endothelial cells (LECs). Capillary-like tube formation of LECs and their proliferation were stimulated by both VEGFA and LH. IGFBP7 treatment suppressed VEGFA- or LH-induced tube formation. The proliferation and migration of LECs, and phosphorylation of mitogen-activated protein kinase kinase and extracellular signal-regulated kinase 1/2 were inhibited by IGFBP7. Furthermore, IGFBP7 attenuated VEGFA-enhanced cyclooxygenase (COX)-2 mRNA expression and prostaglandin E2 secretion. These findings suggest the possibility that luteal IGFBP7 secretion may suppress the stimulatory effect of VEGFA on angiogenesis in the early CL.
发育中的黄体(CL)血管生成是早期妊娠建立和维持的先决条件。为了探究胰岛素样生长因子结合蛋白7(IGFBP7)在发育中的黄体中的生理意义,使用分离的黄体微血管内皮细胞(LECs)测试了IGFBP7对血管内皮生长因子(VEGFA)和促黄体生成素(LH)诱导的体外管形成的影响。VEGFA和LH均刺激了LECs的毛细血管样管形成及其增殖。IGFBP7处理抑制了VEGFA或LH诱导的管形成。IGFBP7抑制了LECs的增殖和迁移,以及丝裂原活化蛋白激酶激酶和细胞外信号调节激酶1/2的磷酸化。此外,IGFBP7减弱了VEGFA增强的环氧化酶(COX)-2 mRNA表达和前列腺素E2分泌。这些发现提示黄体IGFBP7分泌可能抑制VEGFA对早期黄体血管生成的刺激作用。