Jo T, Tomiyama T, Ohashi K, Saji F, Tanizawa O, Ozaki M, Yamamoto R, Yamamoto T, Nishizawa Y, Terada N
Department of Obstetrics and Gynecology, Osaka University Medical School, Japan.
Anat Rec. 1995 Jan;241(1):70-6. doi: 10.1002/ar.1092410110.
Macrophages and T lymphocytes have been identified in the regressing corpus luteum, and they are thought to participate in structural luteolysis (destruction and removal of luteal cells). Since these cells produce cytokines such as tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma), we investigated the effects of these two cytokines on death of luteal cells in vitro.
Mouse luteal cells were cultured in serum-free medium with TNF-alpha at 0, 500, 1,000, 3,000, or 5,000 U/ml in the presence or absence of IFN-gamma at 1,000 U/ml for 3 or 6 days. Then, for estimation of the actions of these cytokines on induction of luteal cell death, we determined the number of viable cells, the percentage of fragmented DNA in total DNA extracted from cultured cells, and the percentage of cells with fragmented DNA in their nuclei by the trypan blue exclusion test, the sensitive micromethod for DNA assay, and the in situ DNA 3' end labeling method, respectively. DNA fragmentation was also analysed by agarose gel electrophoresis, and cultured cells were examined by electron microscopy.
On day 3 of culture, IFN-gamma alone at 1,000 U/ml or TNF-alpha alone at 500-5,000 U/ml did not decrease the number of viable cells, but a combination of IFN-gamma (1,000 U/ml) and TNF-alpha (5,000 U/ml) did. On day 6, IFN-gamma alone at 1,000 U/ml or TNF-alpha alone at 500, 1,000 and 3,000 U/ml did not decrease the number of viable cells, whereas TNF-alpha alone at 5,000 U/ml did, and combinations of IFN-gamma and TNF-alpha at 1,000, 3,000, and 5,000 U/ml decreased the number of viable cells in proportion to the concentration of TNF-alpha. On days 3-6 of culture, combinations of IFN-gamma and TNF-alpha that decreased the number of viable cells also increased the percentages of fragmented DNA in total DNA of cultured luteal cells and the percentages of luteal cells with fragmented DNA in their nuclei. Agarose gel electrophoresis of fragmented DNA showed a ladder-like pattern, and electron microscopic examination showed luteal cells with the characteristics of apoptosis.
The presence of IFN-gamma modulates the ability of TNF-alpha to induce a reduction in the number of viable cells, although TNF-alpha alone at high concentrations can induce a reduction in the number of viable cells.
在退化的黄体中已鉴定出巨噬细胞和T淋巴细胞,它们被认为参与了结构性黄体溶解(黄体细胞的破坏和清除)。由于这些细胞会产生细胞因子,如肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ),我们研究了这两种细胞因子对体外黄体细胞死亡的影响。
将小鼠黄体细胞在无血清培养基中培养,分别加入浓度为0、500、1000、3000或5000 U/ml的TNF-α,同时加入或不加入浓度为1000 U/ml的IFN-γ,培养3天或6天。然后,为了评估这些细胞因子对诱导黄体细胞死亡的作用,我们分别通过台盼蓝排斥试验、灵敏的DNA微量分析法和原位DNA 3'末端标记法,测定了活细胞数量、从培养细胞中提取的总DNA中DNA片段化的百分比以及细胞核中DNA片段化的细胞百分比。还通过琼脂糖凝胶电泳分析了DNA片段化情况,并通过电子显微镜检查了培养细胞。
在培养第3天,单独使用1000 U/ml的IFN-γ或单独使用500 - 5000 U/ml的TNF-α不会减少活细胞数量,但1000 U/ml的IFN-γ与5000 U/ml的TNF-α联合使用会减少活细胞数量。在第6天,单独使用1000 U/ml的IFN-γ或单独使用500、1000和3000 U/ml的TNF-α不会减少活细胞数量,而单独使用5000 U/ml的TNF-α会减少活细胞数量,1000、3000和5000 U/ml的IFN-γ与TNF-α联合使用会按TNF-α浓度比例减少活细胞数量。在培养的第3 - 6天,减少活细胞数量的IFN-γ与TNF-α联合使用也增加了培养黄体细胞总DNA中DNA片段化的百分比以及细胞核中DNA片段化的黄体细胞百分比。DNA片段的琼脂糖凝胶电泳显示出梯状模式,电子显微镜检查显示黄体细胞具有凋亡特征。
IFN-γ的存在调节了TNF-α诱导活细胞数量减少的能力,尽管高浓度的TNF-α单独使用也可诱导活细胞数量减少。