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使用紫激发型细胞通透型 DNA 结合染料分离小鼠生精细胞。

Isolation of Murine Spermatogenic Cells using a Violet-Excited Cell-Permeable DNA Binding Dye.

机构信息

Division of Reproductive Sciences, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center; Department of Pediatrics, University of Cincinnati College of Medicine.

Division of Germ Cell Biology, National Institute for Basic Biology, National Institutes of Natural Sciences; Department of Basic Biology, School of Life Science, Graduate University for Advanced Studies (Sokendai).

出版信息

J Vis Exp. 2021 Jan 14(167). doi: 10.3791/61666.

Abstract

Isolation of meiotic spermatocytes is essential to investigate molecular mechanisms underlying meiosis and spermatogenesis. Although there are established cell isolation protocols using Hoechst 33342 staining in combination with fluorescence-activated cell sorting, it requires cell sorters equipped with an ultraviolet laser. Here we describe a cell isolation protocol using the DyeCycle Violet (DCV) stain, a low cytotoxicity DNA binding dye structurally similar to Hoechst 33342. DCV can be excited by both ultraviolet and violet lasers, which improves the flexibility of equipment choice, including a cell sorter not equipped with an ultraviolet laser. Using this protocol, one can isolate three live-cell subpopulations in meiotic prophase I, including leptotene/zygotene, pachytene, and diplotene spermatocytes, as well as post-meiotic round spermatids. We also describe a protocol to prepare single-cell suspension from mouse testes. Overall, the procedure requires a short time to complete (4-5 hours depending on the number of needed cells), which facilitates many downstream applications.

摘要

分离减数分裂精母细胞对于研究减数分裂和精子发生的分子机制至关重要。尽管已经建立了使用 Hoechst 33342 染色结合荧光激活细胞分选分离细胞的既定方案,但它需要配备紫外线激光的细胞分选器。在这里,我们描述了一种使用 DyeCycle Violet(DCV)染色的细胞分离方案,这是一种低细胞毒性的 DNA 结合染料,结构上与 Hoechst 33342 相似。DCV 可以被紫外线和紫光激光激发,这提高了设备选择的灵活性,包括没有配备紫外线激光的细胞分选器。使用该方案,可以分离减数分裂前期 I 中的三种活细胞亚群,包括细线期/合线期、粗线期和双线期精母细胞,以及减数分裂后的圆形精子细胞。我们还描述了一种从小鼠睾丸制备单细胞悬液的方案。总体而言,该程序完成时间较短(根据所需细胞的数量,需要 4-5 小时),这有利于许多下游应用。

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