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Tissue culture before transplantation of frozen-thawed human fetal ovarian tissue into immunodeficient mice.

机译:将冻融的人胎儿卵巢组织移植到免疫缺陷小鼠中之前的组织培养。

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OBJECTIVE: To evaluate the effects of tissue culture on the viability and development of follicles in frozen-thawed human fetal ovarian tissue before transplantation into severe combined immunodeficient (SCID) mice and to determine the optimal duration of pretransplant tissue culture. DESIGN: Experimental prospective study. SETTING: Animal center and reproductive laboratories in university hospitals. INTERVENTION(S): Frozen-thawed human fetal ovarian tissue samples from 20-week-old abortuses were randomly divided into four groups and cultured in vitro for 0, 3, 6, or 9 days before being xenografted into kidney capsules of bilaterally oophorectomized severe combined immunodeficient (SCID) mice. Grafts were removed 16 weeks after transplantation. Histological analysis and assessment of proliferative cell nuclear antigen (PCNA) expression levels were used to evaluate the survival and development of follicles. RESULT(S): The proportion of growing follicles was significantly increased in groups cultured before transplantation as compared with the noncultured group. Sixteen weeks after transplantation, the number of follicles in the cultured grafts was higher than that in the noncultured grafts. Grafts cultured for 6 or 9 days showed higher proportions of preantral and antral follicles than grafts cultured for 0 or 3 days. PCNA immunohistochemical analysis indicated that follicle cells were in a proliferative state after culture and transplantation. CONCLUSION(S): The viability and development of human fetal follicles may be improved by pretransplant tissue culture. The optimal culture duration before transplantation of fetal ovarian tissue is 6 days.
机译:目的:评估组织培养对冻融人胎儿卵巢组织移植入重度合并免疫缺陷(SCID)小鼠前的存活力和卵泡发育的影响,并确定移植前组织培养的最佳持续时间。设计:实验性前瞻性研究。地点:大学医院的动物中心和生殖实验室。干预:将来自20周龄流产的冻融的人类胎儿卵巢组织样品随机分为四组,并在体外培养0、3、6或9天,然后异种移植到双侧经卵巢切除的严重肾脏肾脏胶囊中。联合免疫缺陷(SCID)小鼠。移植后16周将移植物移出。组织学分析和评估增殖细胞核抗原(PCNA)表达水平来评估卵泡的存活和发育。结果:与未培养组相比,移植前培养组的卵泡生长比例显着增加。移植后十六周,培养的移植物中的卵泡数量高于未培养的移植物中的卵泡数量。培养6或9天的移植物比培养0或3天的移植物显示出更高的窦前和肛门卵泡比例。 PCNA免疫组织化学分析表明,培养和移植后的卵泡细胞处于增殖状态。结论:移植前的组织培养可以改善人胎儿卵泡的活力和发育。胎儿卵巢组织移植前的最佳培养时间为6天。

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