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Isolation of spermatozoa with low levels of fragmented DNA with the use of flow cytometry and sorting

机译:使用流式细胞仪和分选技术分离具有低水平片段化DNA的精子

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摘要

Objective To develop a method to select spermatozoa with low DNA fragmentation rates for assisted reproduction technologies (ART). Design Multistep prospective cohort study. Setting University hospital. Patient(s) Semen samples of 34 infertile men were prepared in parallel with swim-up and fluorescence-activated cell sorting (FACS), and 11 semen samples were used for testing the staining strategy. Intervention(s) Flow cytometric sorting of YO-PRO-stained spermatozoa. Main Outcome Measure(s) Assessment of recovery of spermatozoa and purity after sorting, quantification of sperm DNA fragmentation and viability after sorting and after swim up preparation. Result(s) Staining with YO-PRO could be performed successfully in regular culture medium, both dead and apoptotic spermatozoa were labeled without the dye entering the viable spermatozoa. Compared with the conventional swim-up method, the sorted viable population showed a significantly reduced number of spermatozoa with fragmented DNA. Conclusion(s) A novel method has been developed, which not only might improve the outcome of ART, but can also help to clarify the ongoing controversy of the role of DNA fragmentation in male infertility.
机译:目的开发一种选择低DNA片段化率的精子用于辅助生殖技术的方法。设计多步前瞻性队列研究。设置大学医院。平行于游泳和荧光激活细胞分选(FACS)制备了34例不育男性患者的精液样本,并使用11个精液样本测试了染色策略。干预措施YO-PRO染色的精子的流式细胞仪分选。主要结果测量评估分选后精子的回收率和纯度,分选后和游泳准备后精子DNA片段的定量和活力的定量。结果可以在常规培养基上成功进行YO-PRO染色,标记死去的和凋亡的精子,而染料不进入活的精子。与传统的游泳方法相比,分选出的存活种群显示具有片段化DNA的精子数量明显减少。结论已开发出一种新方法,该方法不仅可以改善抗逆转录病毒疗法的疗效,而且还可以帮助阐明DNA片段化在男性不育症中的作用的争议。

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