Alonso-Pozos Israel, Rosales-Torres Ana Maria, Avalos-Rodríguez Alejandro, Vergara-Onofre Marcela, Rosado-García Adolfo
Departamento de Producción Agrícola y Animal, Laboratorio de Bioquímica de la Reproducción, Universidad Autónoma Metropolitana, Unidad Xochimilco, Calzada del Hueso 1100, Col. Villa Quietud, Delegación Coyocán, México 04960, Mexico DF.
Theriogenology. 2003 Oct 1;60(6):1071-81. doi: 10.1016/s0093-691x(03)00123-7.
Changes in granulosa cell lysosomal and mitochondrial functions in relation to follicular size and to the stage of atresia were studied by fluorescent emission spectra and intensity using flow cytometry. Antral follicles were grouped by size in two groups: small, 3-6 mm and large, >6mm in diameter, and classified into three stages of atresia: non-atretic, initially atretic and advanced atretic. Differences in Rhodamine 123 (Rh123) and Acridine Orange (AO) fluorescent intensity indicated that changes in mitochondrial function are the primary mechanism of granulosa cell death in atretic follicles 3-6 mm in diameter, while its role in granulosa cell death in >6 mm atretic follicles seemed to be less important. However, modifications in lysosomal function (shown by a decrease in fluorometric intensity of AO incubated granulosa cells) were mainly associated with cell death in large atretic follicles. Our results support the hypothesis that the pathway of granulosa cell death during follicular atresia depends on the state of energy metabolism or on the production of hypoxic conditions related to follicular size. Changes in mitochondrial membrane potential and production of permeability transition pores were the main changes found in small follicles, while lysosomal function destabilization seemed to be the major cause of granulosa cell death during atresia in large follicles.
利用流式细胞术通过荧光发射光谱和强度研究了颗粒细胞溶酶体和线粒体功能与卵泡大小及闭锁阶段的关系。将窦状卵泡按大小分为两组:小卵泡,直径3 - 6mm;大卵泡,直径>6mm,并分为三个闭锁阶段:非闭锁、初始闭锁和晚期闭锁。罗丹明123(Rh123)和吖啶橙(AO)荧光强度的差异表明,线粒体功能变化是直径3 - 6mm闭锁卵泡中颗粒细胞死亡的主要机制,而其在直径>6mm闭锁卵泡颗粒细胞死亡中的作用似乎不那么重要。然而,溶酶体功能的改变(通过AO孵育的颗粒细胞荧光强度降低显示)主要与大的闭锁卵泡中的细胞死亡有关。我们的结果支持这样的假设,即卵泡闭锁期间颗粒细胞死亡途径取决于能量代谢状态或与卵泡大小相关的缺氧条件的产生。线粒体膜电位的变化和通透性转换孔的产生是在小卵泡中发现的主要变化,而溶酶体功能不稳定似乎是大卵泡闭锁期间颗粒细胞死亡的主要原因。