Peng C, Huang T H, Jeung E B, Donaldson C J, Vale W W, Leung P C
Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada.
Endocrinology. 1993 Dec;133(6):3046-9. doi: 10.1210/endo.133.6.8243335.
Activin has been suggested to be an autocrine/paracrine regulator in the human placenta. In the present study, we examined the expression of the gene encoding activin type II receptor (ActRII) in this tissue. Using primers corresponding to the published sequence of human ActRII, a 456bp fragment was obtained from cDNAs prepared from the placenta, as well as the ovary and brain, by polymerase chain reaction (PCR). Southern blot hybridization of the PCR products and DNA cloning and sequencing confirmed that the product is the authentic ActRII. Trophoblast cells prepared from both first trimester and term placentae expressed the ActRII gene. When trophoblast cells from term placenta were separated into syncytiotrophoblast- and cytotrophoblast-enriched fractions and incubated for 1-6 days, ActRII gene expression was observed in both cell preparations, with the syncytiotrophoblast-enriched fraction having higher levels of expression at days 1, 3, and 4. These results provide the first direct evidence that the activin type II receptor mRNA is present in human trophoblast cells and strengthen the hypothesis that activin is an autocrine/paracrine regulator of placental function. To our knowledge, this is also the first report that the ActRII gene is expressed in the human brain and ovary.
已有研究表明,激活素是人类胎盘中的一种自分泌/旁分泌调节因子。在本研究中,我们检测了编码激活素II型受体(ActRII)的基因在该组织中的表达情况。使用与已发表的人类ActRII序列相对应的引物,通过聚合酶链反应(PCR)从胎盘、卵巢和大脑制备的cDNA中获得了一个456bp的片段。PCR产物的Southern印迹杂交以及DNA克隆和测序证实该产物为 authentic ActRII。从孕早期和足月胎盘制备的滋养层细胞均表达ActRII基因。当将足月胎盘的滋养层细胞分离为富含合体滋养层细胞和细胞滋养层细胞的组分,并培养1 - 6天时,在两种细胞制备物中均观察到ActRII基因表达,其中富含合体滋养层细胞的组分在第1、3和4天表达水平较高。这些结果提供了首个直接证据,表明激活素II型受体mRNA存在于人类滋养层细胞中,并强化了激活素是胎盘功能的自分泌/旁分泌调节因子这一假说。据我们所知,这也是ActRII基因在人类大脑和卵巢中表达的首次报道。