The effects of co-culture of human spermatozoa with human immortalized endometrial cells - epithelial or stromal - on sperm movement characteristics, including hyperactivation, were studied using computer-assisted sperm analysis (CASA). Epithelial and stromal cell types could be separated following 8-10 days of culture of endometrial cells originating from human biopsies. Both cell types were immortalized by the SV 40 large T antigen. Co-incubation of sperm with epithelial and stromal monolayers enhanced the rate of hyperactivation24.9% (P <0.05) and 17.8% (P = 0.05) versus 9.5% as control, respectively, whereas the majority of motility parameters remained unchanged. Conditioned media had no effect upon sperm parameters, including hyperactivation. Co-incubation with either monolayer was able to maintain sperm motility over a longer period than incubation in control medium alone.

In four patients whose spermatozoa did not exhibit hyperactivation, co-incubation with epithelial cells, but not conditioned medium, allowed normal rates of hyperactivation (range6.9-15.6%).

译文

使用计算机辅助精子分析 (CASA) 研究了人类精子与人类永生化的子宫内膜细胞 (上皮或基质) 共培养对精子运动特征 (包括过度活化) 的影响。在培养源自人活检的子宫内膜细胞8-10天后,可以分离上皮和基质细胞类型。两种细胞类型都被SV 40大T抗原永生化。与9.5% 对照相比,将精子与上皮和基质单层共同孵育可分别提高高激活率24.9% (P <0.05) 和17.8% (P = 0.05),而大多数运动参数保持不变。条件培养基对精子参数 (包括过度活化) 没有影响。与单独在对照培养基中孵育相比,与任一单层共同孵育能够在更长的时间内保持精子活力。
在四名精子未表现出过度活化的患者中,与上皮细胞共同孵育,但不是条件培养基,允许正常的过度激活率 (范围6.9-15.6%)。

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