Dhara S, Lalitkumar P G, Sengupta J, Ghosh D
Department of Physiology, All India Institute of Medical Sciences, New Delhi 110029, India.
Mol Hum Reprod. 2001 Apr;7(4):365-71. doi: 10.1093/molehr/7.4.365.
There are various cellular mediators which can affect the process of blastocyst implantation by regulating the proliferation and differentiation of conceptus and maternal endometrial cells. Insulin-like growth factors I (IGF-I) and II (IGF-II) are potent mitogenic and differentiation-promoting growth factors. However, the role of IGF peptides at implantation in primate species is not well understood. The objective of the present study was to immunohistochemically localize IGF-I and IGF-II peptides in trophoblast cells and maternal endometrial cells during lacunar and villous stages of placentation in the Rhesus monkey. Female animals (n = 10) were laparotomized on estimated days 13-16 after fertilization to collect primary implantation sites which were subjected to immunohistochemical staining for IGF-I and IGF-II peptides. Cell-type specificity for IGF-I and IGF-II was evident with a very low level of IGF-I peptide immunolocalized in trophoblast cells lining lacunae, and primary and secondary villi, while moderate to high amounts of IGF-II peptide were detected in lamellar syncytiotrophoblast cells lining lacunae, early villi and cell columns, as well as in migrating trophoblast cells in the extravillous compartment and in endovascular trophoblast cells. The observed presence of IGF-II peptide in differentiated lamellar syncytiotrophoblast cells during the very early stages of implantation and placentation in the Rhesus monkey may be important in their transition to this differentiated cell population. Maternal endometrial cells showed similar distribution profiles for IGF-I and IGF-II. In conclusion, we report differential distribution of IGF-I and IGF-II peptides in trophoblast cell populations at the feto-maternal interface during lacunar and villous stages of gestation in the Rhesus monkey.
有多种细胞介质可通过调节孕体和母体子宫内膜细胞的增殖与分化来影响囊胚着床过程。胰岛素样生长因子I(IGF-I)和II(IGF-II)是强有力的促有丝分裂和促进分化的生长因子。然而,IGF肽在灵长类动物着床过程中的作用尚未完全明确。本研究的目的是通过免疫组织化学方法定位恒河猴胎盘形成的血窦期和绒毛期滋养层细胞和母体子宫内膜细胞中的IGF-I和IGF-II肽。对10只雌性动物在受精后估计的第13 - 16天进行剖腹手术,收集初级着床部位,对其进行IGF-I和IGF-II肽的免疫组织化学染色。IGF-I和IGF-II的细胞类型特异性很明显,在血窦、初级和次级绒毛内衬的滋养层细胞中,IGF-I肽的免疫定位水平非常低,而在血窦、早期绒毛和细胞柱内衬的片状合体滋养层细胞中,以及在绒毛外间隙的迁移滋养层细胞和血管内滋养层细胞中,检测到中等至大量的IGF-II肽。在恒河猴着床和胎盘形成的极早期,在分化的片状合体滋养层细胞中观察到IGF-II肽的存在,这可能对它们向这种分化细胞群体的转变很重要。母体子宫内膜细胞中IGF-I和IGF-II的分布情况相似。总之,我们报告了在恒河猴妊娠的血窦期和绒毛期,胎儿 - 母体界面滋养层细胞群体中IGF-I和IGF-II肽的差异分布。