INTRAPLACENTAL PATHWAY MODULATING TROPHOBLAST CELLS

胎盘内途径调节滋养层细胞

• 批准号: 6041430
• 负责人: GUOLI DAI
• 金额: $ 7.5万
• 依托单位: UNIVERSITY OF KANSAS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-01-12 至 2001-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6041430
• 关键词: alkaline phosphatase; biological signal transduction; cell differentiation; cell proliferation; chimeric proteins; female; laboratory rat; placenta; pregnancy; prolactin; protein binding; protein structure function; receptor expression; trophoblast

The long-term objective of the research is to further our understanding of the establishment and maintenance of pregnancy. We focus on the actions of signaling molecules originating in the placenta. Members of a family of proteins related to prolactin (PRL) are expressed in cell- and temporal- specific patterns in the uteroplacental compartment and have been shown to play a pivotal role in the establishment and maintenance of pregnancy. Prolactin-like protein-C variant (PLP-Cv) is new member of the family identified in recent years. It is expressed specifically in trophoblast giant cells and spongiotrophoblast cells of the rat placenta during the second half of gestation. Using an alkaline phosphatase (AP)-PLP-Cv fusion protein, we found that PLP-Cv exclusively bound to trophoblast giant cells and spongiotrophoblast cells within the junctional zone of the rat placenta. Thus, the same cells that produce PLP-Cv are also targets for PLP-Cv are also targets for PLP-Cv action. We hypothesize that PLP-Cv may be an autocrine/paracrine factor involved in the regulation of placental development/function. The Rcho-1 trophoblast cell lines has been proven to be a very useful model to investigate trophoblast cell development. We propose to utilize the Rcho-1 trophoblast cell line as an in vitro model to evaluate the effects of PLP-Cv on trophoblast cell proliferation and differentiation. We will also isolate the trophoblast cell receptor for PLP-Cv using an expression cloning strategy with the AP- PLP-Cv fusion protein as a probe. These findings will further our understanding of the intraplacental regulatory network involved in the control of placental development and maintenance of pregnancy.

该研究的长期目标是进一步了解妊娠的建立和维持。我们关注源自胎盘的信号分子的作用。与催乳素 (PRL) 相关的蛋白质家族成员在子宫胎盘室中以细胞和时间特异性模式表达，并已被证明在妊娠的建立和维持中发挥着关键作用。催乳素样蛋白-C 变体（PLP-Cv）是近年来发现的该家族的新成员。它在妊娠后半期的大鼠胎盘的滋养层巨细胞和海绵滋养层细胞中特异性表达。使用碱性磷酸酶（AP）-PLP-Cv 融合蛋白，我们发现 PLP-Cv 专门与大鼠胎盘交界区内的滋养层巨细胞和海绵滋养层细胞结合。因此，产生 PLP-Cv 的相同细胞也是 PLP-Cv 的靶标，也是 PLP-Cv 作用的靶标。我们假设 PLP-Cv 可能是参与胎盘发育/功能调节的自分泌/旁分泌因子。 Rcho-1 滋养层细胞系已被证明是研究滋养层细胞发育的非常有用的模型。我们建议利用 Rcho-1 滋养层细胞系作为体外模型来评估 PLP-Cv 对滋养层细胞增殖和分化的影响。我们还将使用 AP-PLP-Cv 融合蛋白作为探针的表达克隆策略分离 PLP-Cv 的滋养层细胞受体。 这些发现将进一步加深我们对参与控制胎盘发育和维持妊娠的胎盘内调节网络的理解。