Nicola Catalin, Chirpac Andrei, Lala Peeyush K, Chakraborty Chandan
Department of Anatomy, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada N6A 5C1.
Endocrinology. 2008 Mar;149(3):1243-51. doi: 10.1210/en.2007-1136. Epub 2007 Dec 13.
Prostaglandin (PG) E(2) may regulate invasiveness of human placenta because we previously reported stimulation of migration of placental trophoblasts by PGE(2) acting through PGE receptor (EP)-1 and activating calpain. RhoA GTPase and its important effector Rho kinase (ROCK) have also been previously shown to regulate trophoblast migration. Using immortalized HTR-8/SVneo trophoblast cells and first-trimester human chorionic villus explant cultures on matrigel, we further examined the role of RhoA/ROCK and MAPK (ERK1/2) pathways on PGE(2)-mediated stimulation of trophoblast migration. Migration of cytotrophoblasts was shown to be inhibited by treatment of the trophoblast cell line and chorionic villus explants with either cell-permeable C3 transferase or selective RhoA small interfering RNA. These inhibitions were significantly mitigated by the addition of PGE(2), an EP1/EP3 agonist or an EP3/EP4 agonist, suggesting that RhoA plays an important role in trophoblast migration but may not be obligatory for PGE(2) action. Treatment of HTR-8/SVneo cells with nonselective ROCK inhibitor Y27632 or ROCK small interfering RNAs inhibited migration of these cells, which could not be rescued with PGE(2) or the other two EP agonists, suggesting the obligatory role of ROCK in PGE(2)-induced migratory response. Furthermore, U0126, an inhibitor of MAPK kinases MEK1 and MEK2, abrogated PGE(2)-induced migration of trophoblasts, and PGE(2) or the other two EP agonists stimulated ERK1/2 activation in trophoblasts, which was not abrogated by pretreatment with C3 transferase, indicating that ERK signaling pathway is an efficient alternate pathway for RhoA in PGE(2)-mediated migration of trophoblasts. These results suggest that ROCK and ERK1/2 play more important roles than RhoA in PGE(2)-mediated migration stimulation of first-trimester trophoblasts.
前列腺素(PG)E2可能调节人胎盘的侵袭性,因为我们之前报道过PGE2通过前列腺素E受体(EP)-1发挥作用并激活钙蛋白酶,从而刺激胎盘滋养层细胞迁移。RhoA GTP酶及其重要效应器Rho激酶(ROCK)此前也已被证明可调节滋养层细胞迁移。我们使用永生化的HTR-8/SVneo滋养层细胞以及在基质胶上培养的孕早期人绒毛膜绒毛外植体,进一步研究了RhoA/ROCK和丝裂原活化蛋白激酶(MAPK,细胞外信号调节激酶1/2,ERK1/2)信号通路在PGE2介导的滋养层细胞迁移刺激中的作用。用细胞可渗透的C3转移酶或选择性RhoA小干扰RNA处理滋养层细胞系和绒毛膜绒毛外植体,结果显示细胞滋养层细胞的迁移受到抑制。添加PGE2、EP1/EP3激动剂或EP3/EP4激动剂可显著减轻这些抑制作用,这表明RhoA在滋养层细胞迁移中起重要作用,但可能不是PGE2发挥作用所必需的。用非选择性ROCK抑制剂Y27632或ROCK小干扰RNA处理HTR-8/SVneo细胞会抑制这些细胞的迁移,而PGE2或其他两种EP激动剂无法挽救这种抑制作用,这表明ROCK在PGE2诱导的迁移反应中起必需作用。此外,MAPK激酶MEK1和MEK2的抑制剂U0126消除了PGE2诱导的滋养层细胞迁移,并且PGE2或其他两种EP激动剂刺激了滋养层细胞中ERK1/2的激活,而C3转移酶预处理并未消除这种激活,这表明ERK信号通路是PGE2介导的滋养层细胞迁移中RhoA的有效替代通路。这些结果表明,在PGE2介导的孕早期滋养层细胞迁移刺激中,ROCK和ERK1/2比RhoA发挥更重要的作用。