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注射圆形精子细胞的兔卵母细胞足月发育的激活方案。

Activation regimens for full-term development of rabbit oocytes injected with round spermatids.

作者信息

Hirabayashi Masumi, Kato Megumi, Kitada Kensaku, Ohnami Naoko, Hirao Masao, Hochi Shinichi

机构信息

Section of Mammalian Transgenesis, Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.

出版信息

Mol Reprod Dev. 2009 Jun;76(6):573-9. doi: 10.1002/mrd.20984.

Abstract

The present study was designed to investigate the effect of activation regimens on full-term development of rabbit oocytes after round spermatid injection (ROSI). In the first series, rabbit oocytes were treated with 5 microM ionomycin before ROSI, after ROSI, or before and after ROSI. In addition, non-treated oocytes were subjected to intracytoplasmic sperm injection (ICSI) using ejaculated spermatozoa. Cleavage rate of ROSI oocytes activated before and after ROSI (55%) was comparable with that of ICSI oocytes (60%), and significantly higher than those of ROSI oocytes activated either before or after ROSI (29-39%; P < 0.05). No offspring were produced by transfer of the cleaving ROSI oocytes, while 8% of the cleaving ICSI oocytes transferred gave birth to offspring. In the second series, oocytes were exposed to 5, 10, or 20 microM ionomycin, followed by ROSI, 5 microM ionomycin treatment, and incubation with 5 microg/ml cycloheximide (CHX) + 2 mM 6-dimethylaminopurine (DMAP). Significantly higher cleavage rates were derived from oocytes activated with 10 and 20 microM ionomycin before ROSI (91% and 82%, respectively; P < 0.05) compared to those activated with 5 microM ionomycin before ROSI (53%). Live offspring were obtained when the cleaving ROSI oocytes with the initial ionomycin treatment at 5 and 10 microM were transferred (offspring rate 2% and 4%, respectively). These activation regimens, however, were not valid for the ROSI using cryopreserved round spermatids. In conclusion, rabbit ROSI oocytes were capable of developing into full-term when the oocytes were activated with a combined treatment of ionomycin and CHX/DMAP.

摘要

本研究旨在探讨激活方案对圆形精子细胞注射(ROSI)后兔卵母细胞足月发育的影响。在第一组实验中,兔卵母细胞在ROSI前、ROSI后或ROSI前后用5微摩尔离子霉素处理。此外,未处理的卵母细胞使用射出的精子进行胞浆内精子注射(ICSI)。ROSI前后激活的ROSI卵母细胞的分裂率(55%)与ICSI卵母细胞的分裂率(60%)相当,且显著高于仅在ROSI前或ROSI后激活的ROSI卵母细胞的分裂率(29%-39%;P<0.05)。分裂的ROSI卵母细胞移植后未产生后代,而移植的分裂ICSI卵母细胞中有8%产下后代。在第二组实验中,卵母细胞分别暴露于5、10或20微摩尔离子霉素,然后进行ROSI、5微摩尔离子霉素处理,并与5微克/毫升放线菌酮(CHX)+2毫摩尔6-二甲基氨基嘌呤(DMAP)一起孵育。与ROSI前用5微摩尔离子霉素激活的卵母细胞(53%)相比,ROSI前用10和20微摩尔离子霉素激活的卵母细胞的分裂率显著更高(分别为91%和82%;P<0.05)。当移植最初用5和10微摩尔离子霉素处理的分裂ROSI卵母细胞时获得了活体后代(后代率分别为2%和4%)。然而,这些激活方案对使用冷冻保存的圆形精子细胞的ROSI无效。总之,当卵母细胞用离子霉素和CHX/DMAP联合处理激活时,兔ROSI卵母细胞能够发育至足月。

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