Nachtigall M J, Kliman H J, Feinberg R F, Olive D L, Engin O, Arici A
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
J Clin Endocrinol Metab. 1996 Feb;81(2):801-6. doi: 10.1210/jcem.81.2.8636307.
Leukemia inhibitory factor (LIF) is a multifunctional glycoprotein strongly associated with normal implantation in the mouse. We have recently determined that LIF is expressed in the human endometrium in a menstrual cycle dependent manner. Maximal expression is observed between days 19 and 25 of the menstrual cycle, coinciding with the time of human implantation. In this study we have utilized purified cultures of human cytotrophoblasts to examine the effects of LIF on several morphologic and biochemical markers of the trophoblastic differentiation. We purified human cytotrophoblasts from term placentae and cultured them with and without LIF (10 ng/mL). The secretion of human CG, oncofetal fibronectin, and progesterone were measured at 24, 48, 72, and 96 h. Northern blot analysis was used to assess messenger RNA (mRNA) expression of beta hCG and oncofetal fibronectin. We found that LIF markedly decreased trophoblast production of hCG protein at 72 and 96 h, as well as expression of beta hCG mRNA. LIF also significantly increased the expression of oncofetal fibronectin mRNA and secretion of the protein. LIF did not affect steroidogenic activity of cultured trophoblasts, as determined by progesterone production. These biochemical changes are characteristic of cytotrophoblast differentiation toward an anchoring extravillous phenotype. Thus, LIF appears to be an important regulator of human embryonic implantation by directly modulating trophoblast differentiation.
白血病抑制因子(LIF)是一种与小鼠正常着床密切相关的多功能糖蛋白。我们最近确定LIF在人类子宫内膜中以月经周期依赖性方式表达。在月经周期的第19至25天观察到最大表达,这与人类着床时间一致。在本研究中,我们利用纯化的人细胞滋养层细胞培养物来研究LIF对滋养层细胞分化的几种形态学和生化标志物的影响。我们从足月胎盘中纯化人细胞滋养层细胞,并在有和没有LIF(10 ng/mL)的情况下进行培养。在24、48、72和96小时测量人绒毛膜促性腺激素(hCG)、癌胚纤连蛋白和孕酮的分泌。使用Northern印迹分析来评估β-hCG和癌胚纤连蛋白的信使核糖核酸(mRNA)表达。我们发现LIF在72和96小时显著降低了滋养层细胞hCG蛋白的产生以及β-hCG mRNA的表达。LIF还显著增加了癌胚纤连蛋白mRNA的表达和该蛋白的分泌。如通过孕酮产生所确定的,LIF不影响培养的滋养层细胞的类固醇生成活性。这些生化变化是细胞滋养层细胞向锚定绒毛外表型分化的特征。因此,LIF似乎通过直接调节滋养层细胞分化而成为人类胚胎着床的重要调节因子。