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通过与非洲绿猴肾细胞进行体外共培养实现人类初级精母细胞减数分裂的完成。

Completion of meiosis in human primary spermatocytes through in vitro coculture with Vero cells.

作者信息

Tanaka Atsushi, Nagayoshi Motoki, Awata Shoichiro, Mawatari Yoshifumi, Tanaka Izumi, Kusunoki Hiroshi

机构信息

Saint Mother Obstetrics and Gynecology and Institute for ART, Fukuoka, Japan.

出版信息

Fertil Steril. 2003 Mar;79 Suppl 1:795-801. doi: 10.1016/s0015-0282(02)04833-1.

Abstract

OBJECTIVE

To examine whether human primary spermatocytes will develop into round spermatids after completing meiosis in an in vitro coculture with Vero cells.

DESIGN

Prospective, controlled in vitro study.

SETTING

A private infertility clinic and a university laboratory.

PATIENT(S): Five azoospermic men whose spermatogenesis was proved to be arrested at the level of the primary spermatocyte in open biopsies.

INTERVENTION(S): In vitro coculture of isolated primary spermatocytes with Vero cells and chromosomal analysis for assessment of the completion of meiosis.

MAIN OUTCOME MEASURE(S): Isolated primary spermatocytes were cocultured with Vero cells under various conditions. The number of chromosomes and chromatids in newly generated cells was determined by Giemsa staining after the cells were injected into mouse oocytes.

RESULT(S): The generation rates of round spermatids in six types of in vitro culture with Vero cells were 0%-10% (highest rates of division were in minimum essential medium (MEM) + 50% boar rete testicular fluid or in human synthetic oviduct fluid + 10% human serum). The number of chromosomes and chromatids in the newly developed cells was 23.

CONCLUSION(S): A single primary spermatocyte was observed to divide into four cells during in vitro coculture with Vero cells. These newly developed cells were proved to be round spermatids by chromosomal analysis. It was verified that a primary spermatocyte developed into round spermatids after completing two cycles of meiosis through in vitro culture.

摘要

目的

研究人类初级精母细胞在与Vero细胞共培养的体外环境中完成减数分裂后是否会发育为圆形精子细胞。

设计

前瞻性对照体外研究。

地点

一家私立不孕不育诊所和一所大学实验室。

患者

5名无精子症男性,经开放性活检证实其精子发生停滞在初级精母细胞阶段。

干预措施

将分离出的初级精母细胞与Vero细胞进行体外共培养,并进行染色体分析以评估减数分裂的完成情况。

主要观察指标

将分离出的初级精母细胞在不同条件下与Vero细胞共培养。将细胞注入小鼠卵母细胞后,通过吉姆萨染色确定新生成细胞中的染色体和染色单体数量。

结果

在六种与Vero细胞的体外培养类型中,圆形精子细胞的生成率为0%-10%(在最低限度基本培养基(MEM)+50%公猪睾丸网液或人类合成输卵管液+10%人血清中分裂率最高)。新发育细胞中的染色体和染色单体数量为23条。

结论

在与Vero细胞的体外共培养过程中,观察到单个初级精母细胞分裂为四个细胞。通过染色体分析证明这些新发育的细胞为圆形精子细胞。证实了初级精母细胞通过体外培养完成两个减数分裂周期后发育为圆形精子细胞。

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