Hashii K, Fujiwara H, Yoshioka S, Kataoka N, Yamada S, Hirano T, Mori T, Fujii S, Maeda M
Department of Gynecology and Obstetrics, Faculty of Medicine, Kyoto University, Japan.
Hum Reprod. 1998 Oct;13(1O):2738-44. doi: 10.1093/humrep/13.10.2738.
Human luteal cells have been reported to express human leukocyte antigen-DR and lymphocyte functional antigen-3 on the cell surface, suggesting physiological interaction between luteal cells and T-lymphocytes through the menstrual cycle into early pregnancy. To elucidate the role of peripheral lymphocytes on corpus luteum differentiation, the effect of peripheral blood mononuclear cells (PBMC) on steroidogenesis by luteal cells was investigated. The production of Th-2 cytokines such as interleukin (IL)-4 and IL-10 by the co-cultured cells was also examined, and the effects of these cytokines on progesterone production by luteal cells were investigated. Corpora lutea were obtained from eight non-pregnant women in the luteal phase and five women in early pregnancy for luteal cell culture. PBMC were isolated from unrelated women in the follicular phase, secretory phase, and early pregnancy. After coculture with allogenic PBMC for 48 h, progesterone production was significantly enhanced by PBMC from the secretory phase and early pregnancy in the non-pregnant luteal cell culture. In the pregnant luteal cell culture, a significant increase in progesterone production was also observed by the co-culture with PBMC from women in early pregnancy, showing that PBMC have a luteotrophic effect. The stimulatory effects of PBMC were also observed in co-culture conditions which prevented direct cell-to-cell interaction with luteal cells, showing the minor influence of mixed lymphocyte reaction. By co-culture with PBMC, the production of IL-10, but not IL-4, was significantly augmented in luteal cell culture derived from non-pregnant women, whereas the production of both IL-4 and IL-10 was significantly enhanced in the luteal cell culture derived from pregnant women. Moreover, IL-4 and IL-10 promoted progesterone production by cultured luteal cells, especially in the luteal cell culture derived from corpora lutea of early pregnancy. These findings indicate that PBMC stimulate progesterone production by luteal cells and suggest the involvement of PBMC in corpus luteum function and differentiation probably via the Th-2-type lymphocytes.
据报道,人黄体细胞在细胞表面表达人白细胞抗原-DR和淋巴细胞功能抗原-3,这表明在整个月经周期直至妊娠早期,黄体细胞与T淋巴细胞之间存在生理相互作用。为了阐明外周淋巴细胞在黄体分化中的作用,研究了外周血单个核细胞(PBMC)对黄体细胞类固醇生成的影响。还检测了共培养细胞产生的白细胞介素(IL)-4和IL-10等Th-2细胞因子,并研究了这些细胞因子对黄体细胞孕酮生成的影响。从8名处于黄体期的非妊娠妇女和5名妊娠早期妇女获取黄体用于黄体细胞培养。从处于卵泡期、分泌期和妊娠早期的无关妇女中分离PBMC。与同种异体PBMC共培养48小时后,非妊娠黄体细胞培养中,分泌期和妊娠早期的PBMC显著增强了孕酮生成。在妊娠黄体细胞培养中,与妊娠早期妇女的PBMC共培养也观察到孕酮生成显著增加,表明PBMC具有黄体营养作用。在防止与黄体细胞直接细胞间相互作用的共培养条件下也观察到PBMC的刺激作用,表明混合淋巴细胞反应的影响较小。通过与PBMC共培养,非妊娠妇女来源的黄体细胞培养中IL-10的产生显著增加,但IL-4未增加,而妊娠妇女来源的黄体细胞培养中IL-4和IL-10的产生均显著增强。此外,IL-4和IL-10促进培养的黄体细胞产生孕酮,尤其是在妊娠早期黄体来源的黄体细胞培养中。这些发现表明PBMC刺激黄体细胞产生孕酮,并提示PBMC可能通过Th-2型淋巴细胞参与黄体功能和分化。