Wånggren K, Lalitkumar P G, Hambiliki F, Ståbi B, Gemzell-Danielsson K, Stavreus-Evers A
Department of Woman and Child Health, Division of Obstetrics and Gynaecology, Karolinska Institutet, Karolinska University Hospital, S-171 76 Stockholm, Sweden.
Mol Hum Reprod. 2007 Jun;13(6):391-7. doi: 10.1093/molehr/gam013. Epub 2007 Apr 12.
Leukaemia inhibitory factor (LIF) is a cytokine, which is associated with reproductive processes such as embryo development and implantation. The objectives of this study were to detect the presence of LIF receptor (LIFR) and glycoprotein 130 (gp 130) in the human Fallopian tube, endometrium and preimplantation embryo and to study the effect of mifepristone on the expression of LIFR and gp130 in the Fallopian tube. Twenty-two healthy fertile women received a single dose of 200 mg mifepristone or placebo immediately after ovulation (LH + 2). Biopsies were obtained from the Fallopian tubes during laparoscopic sterilization once between days LH + 4 and LH + 6 and from endometrium once between days LH + 6 and LH + 8. Preimplantation embryos were received from couples undergoing in vitro fertilization treatment. Immunohistochemistry was used to detect the presence of LIFR and gp130 in the Fallopian tube, endometrium and preimplantation embryo. Real-time PCR was used to study LIFR and gp130 expression in the Fallopian tube and endometrium. LIFR and gp130 were localized in the Fallopian tube, preimplantation embryo and endometrium. LIFR was more abundant in the Fallopian tube than in the endometrium. In the blastocyst, the staining of gp130 was mainly localized in the inner cell mass, whereas LIFR was expressed in all cells. The presence of LIFR and gp130 in the Fallopian tube and preimplantation embryo indicates a role for LIF in communication between the embryo and the Fallopian tube. Mifepristone did not affect the expression of LIFR and gp130 in the Fallopian tube, nor in the endometrium suggesting that progesterone might not be directly involved in the regulation of LIFR or gp130.
白血病抑制因子(LIF)是一种细胞因子,与胚胎发育和着床等生殖过程相关。本研究的目的是检测人输卵管、子宫内膜和植入前胚胎中LIF受体(LIFR)和糖蛋白130(gp130)的存在情况,并研究米非司酮对输卵管中LIFR和gp130表达的影响。22名健康的可育女性在排卵后(LH + 2)立即接受了200 mg米非司酮或安慰剂的单次剂量。在LH + 4至LH + 6天之间进行腹腔镜绝育时从输卵管获取活检组织,在LH + 6至LH + 8天之间从子宫内膜获取一次活检组织。植入前胚胎来自接受体外受精治疗的夫妇。采用免疫组织化学法检测输卵管、子宫内膜和植入前胚胎中LIFR和gp130的存在情况。采用实时PCR法研究输卵管和子宫内膜中LIFR和gp130的表达。LIFR和gp130定位于输卵管、植入前胚胎和子宫内膜中。LIFR在输卵管中的含量高于子宫内膜。在囊胚中,gp130的染色主要定位于内细胞团,而LIFR在所有细胞中均有表达。输卵管和植入前胚胎中LIFR和gp130的存在表明LIF在胚胎与输卵管之间的通讯中发挥作用。米非司酮不影响输卵管和子宫内膜中LIFR和gp130的表达,提示孕酮可能不直接参与LIFR或gp130的调节。