Yanushpolsky E H, Ozturk M, Polgar K, Berkowitz R S, Hill J A
Department of Obstetrics, Gynecology, and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
J Reprod Immunol. 1993 Dec;25(3):235-47. doi: 10.1016/0165-0378(93)90066-q.
The present study was conducted to investigate the effects of cytokines on human chorionic gonadotropin (hCG) and its alpha- and beta-subunit release as well as protein synthesis in a trophoblast cell line. The human choriocarcinoma cell line, Jar, was used as a trophoblast model. Jar cells were incubated for 24 h with varying concentrations (5 x 10(-4)-40 micrograms/ml) of the following cytokines: Il-1, Il-2, Il-3, Il-4, Il-5, Il-6, IFN-gamma, tumor necrosis factor (TNF)-alpha, M-CSF and GM-CSF. Supernatants were assayed for hCG and its alpha- and beta-subunits by immunoradiometric methods. Cytotoxic effects were assessed by trypan blue staining. Protein synthesis was measured by [3H]leucine incorporation. The cytokines Il-1 and TNF-alpha significantly stimulated hCG release. The other cytokines had no significant effect on hCG production. Protein synthesis by the Jar cells was not significantly affected by either Il-1 or TNF-alpha. However, IFN-gamma (40 micrograms/ml) significantly suppressed protein synthesis by the Jar cells. Trophoblast viability in the presence of TNF-alpha (10 micrograms/ml) and IFN-gamma (40 micrograms/ml) was only 40% and 50%, respectively. These results suggest that cytokines may be important regulators of trophoblast function. Il-I appears to have a stimulatory effect on trophoblast hCG release, while TNF-alpha and IFN-gamma appear to have cytotoxic effects on trophoblast cells.
本研究旨在探讨细胞因子对人绒毛膜促性腺激素(hCG)及其α和β亚基释放以及滋养层细胞系中蛋白质合成的影响。人绒毛膜癌细胞系Jar被用作滋养层模型。将Jar细胞与下列细胞因子的不同浓度(5×10⁻⁴ - 40微克/毫升)孵育24小时:白细胞介素-1(Il-1)、白细胞介素-2(Il-2)、白细胞介素-3(Il-3)、白细胞介素-4(Il-4)、白细胞介素-5(Il-5)、白细胞介素-6(Il-6)、γ干扰素(IFN-γ)、肿瘤坏死因子(TNF)-α、巨噬细胞集落刺激因子(M-CSF)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)。通过免疫放射分析方法检测上清液中的hCG及其α和β亚基。通过台盼蓝染色评估细胞毒性作用。通过[³H]亮氨酸掺入法测量蛋白质合成。细胞因子Il-1和TNF-α显著刺激hCG释放。其他细胞因子对hCG产生无显著影响。Jar细胞的蛋白质合成不受Il-1或TNF-α的显著影响。然而,IFN-γ(40微克/毫升)显著抑制Jar细胞的蛋白质合成。在TNF-α(10微克/毫升)和IFN-γ(40微克/毫升)存在下,滋养层细胞活力分别仅为40%和50%。这些结果表明细胞因子可能是滋养层功能的重要调节因子。Il-1似乎对滋养层hCG释放有刺激作用,而TNF-α和IFN-γ似乎对滋养层细胞有细胞毒性作用。