Eldar-Geva T, Rachmilewitz J, de Groot N, Hochberg A
Department of Biological Chemistry, Hebrew University, Jerusalem, Israel.
Placenta. 1993 Mar-Apr;14(2):217-23. doi: 10.1016/s0143-4004(05)80262-0.
Cytotrophoblasts (from term placentae) and cells from the choriocarcinoma cell line JAr were cultivated either separately or in co-culture for 72 h. RNA was isolated from the cell cultures and Northern blots were developed using equal amounts of RNA. The RNA was hybridized with cDNA probes for CG alpha, CG beta and hPL. Corresponding m-RNAs were detected in the three RNAs except for hPL m-RNA which was absent from JAr cells RNA. The abundance of CG alpha and CG beta m-RNA in the RNA of the co-culture was higher than their accumulative abundances in the RNAs from cytotrophoblasts and JAr cells cultured alone and the abundance of hPL m-RNA in the RNA of the co-cultures was as high as that in the RNA from cytotrophoblasts cultured alone. On the basis of previous findings (Hochberg et al, 1991), it can be assumed that the cytotrophoblasts in the co-cultures are responsible for the increase in hormonal m-RNA production. It could be calculated that the abundances of the CG alpha, CG beta and hPL m-RNAs in the RNA which originated in the cytotrophoblast nuclei were 20, 100 and 10-fold higher respectively in the co-culture compared to those in the culture of cytotrophoblasts. This effect is limited to certain genes only as the concentration of the 92kD collagenase m-RNA and uPA (urokinase type plasminogen activator) m-RNA, which are both produced in cytotrophoblasts to a much higher extent than in JAr cells, and are not increased by cultivating the cytotrophoblasts with JAr cells in co-culture.(ABSTRACT TRUNCATED AT 250 WORDS)
将来自足月胎盘的细胞滋养层细胞和绒癌细胞系JAr细胞分别培养或共培养72小时。从细胞培养物中分离RNA,并使用等量的RNA进行Northern印迹分析。RNA与CGα、CGβ和hPL的cDNA探针杂交。在三种RNA中均检测到相应的mRNA,但JAr细胞RNA中未检测到hPL mRNA。共培养物RNA中CGα和CGβ mRNA的丰度高于单独培养的细胞滋养层细胞和JAr细胞RNA中它们的累积丰度,共培养物RNA中hPL mRNA的丰度与单独培养的细胞滋养层细胞RNA中的丰度一样高。根据先前的研究结果(霍奇伯格等人,1991年),可以推测共培养中的细胞滋养层细胞是激素mRNA产生增加的原因。据计算,与细胞滋养层细胞培养相比,共培养中源自细胞滋养层细胞核的RNA中CGα、CGβ和hPL mRNA的丰度分别高出20倍、100倍和10倍。这种效应仅限于某些基因,因为92kD胶原酶mRNA和uPA(尿激酶型纤溶酶原激活剂)mRNA的浓度,这两种mRNA在细胞滋养层细胞中的产生量比在JAr细胞中高得多,并且通过将细胞滋养层细胞与JAr细胞共培养不会增加。(摘要截断于250字)