Porter D A, Harman R M, Cowan R G, Quirk S M
Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.
Reproduction. 2001 Apr;121(4):561-6.
The Fas antigen (Fas) is a cell surface receptor that may be involved in the initiation and progression of follicle cell apoptosis during atresia. Fas initiates apoptosis in sensitive cells after binding Fas ligand (FasL). Other experiments have shown that expression of Fas mRNA and responsiveness to Fas-mediated apoptosis vary in bovine granulosa and theca cells during follicle development. In the present study, FasL mRNA content was measured and Fas and FasL protein expression was examined in bovine granulosa and theca cells of healthy dominant follicles and the two largest atretic subordinate follicles on day 5 of the oestrous cycle (day 0 = oestrus), and of dominant follicles from the first wave of follicle development after they had become atretic and showed no growth for 4 days. FasL mRNA content was higher in granulosa cells from atretic compared with healthy follicles. FasL mRNA content was also higher in theca cells from atretic subordinate compared with healthy dominant follicles on day 5, but did not differ between theca cells from healthy and atretic dominant follicles. Immunohistochemical staining for FasL was more intense in theca compared with granulosa cells and in atretic compared with healthy follicles. Immunohistochemical staining for Fas was more intense in granulosa compared with theca cells and in atretic subordinate compared with healthy dominant follicles on day 5. Immune cells, known to express Fas and FasL, were localized in the theca, but not the granulosa, cell layer of all follicles. Higher concentrations of Fas and FasL in cells from atretic follicles, together with the previous demonstration of increased responsiveness of granulosa cells from subordinate follicles to FasL-induced apoptosis, support a potential role for FasL-mediated apoptosis during ovarian follicle atresia.
Fas抗原(Fas)是一种细胞表面受体,可能参与闭锁过程中卵泡细胞凋亡的起始和进展。Fas与Fas配体(FasL)结合后可在敏感细胞中引发凋亡。其他实验表明,在卵泡发育过程中,牛颗粒细胞和卵泡膜细胞中Fas mRNA的表达以及对Fas介导的凋亡的反应性各不相同。在本研究中,测定了发情周期第5天(第0天=发情期)健康优势卵泡以及两个最大的闭锁次级卵泡,以及卵泡发育第一波中已闭锁且4天未生长的优势卵泡的牛颗粒细胞和卵泡膜细胞中FasL mRNA的含量,并检测了Fas和FasL蛋白的表达。与健康卵泡相比,闭锁卵泡颗粒细胞中的FasL mRNA含量更高。在第5天,与健康优势卵泡相比,闭锁次级卵泡的卵泡膜细胞中FasL mRNA含量也更高,但健康和闭锁优势卵泡的卵泡膜细胞之间没有差异。与颗粒细胞相比,FasL的免疫组织化学染色在卵泡膜细胞中更强,与健康卵泡相比,在闭锁卵泡中更强。与卵泡膜细胞相比,Fas的免疫组织化学染色在颗粒细胞中更强,与健康优势卵泡相比,在第5天的闭锁次级卵泡中更强。已知表达Fas和FasL的免疫细胞位于所有卵泡的卵泡膜细胞层,而非颗粒细胞层。闭锁卵泡细胞中Fas和FasL浓度较高,以及先前证明次级卵泡颗粒细胞对FasL诱导的凋亡反应性增加,支持了FasL介导的凋亡在卵巢卵泡闭锁过程中的潜在作用。