长期培养诱导大鼠植入前胚胎中Bax依赖性细胞凋亡。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Kazuomi Nakamura, Misako Seno, Yuki Yoshimura, Osamu Suzuki
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引用次数: 0

摘要

尽管大鼠植入前胚胎是生产转基因大鼠所必需的,但它们的体外培养仍然是一个挑战。大鼠受精卵可以在体外从单细胞期发育到胚泡期;然而,长期文化通过一种未知的机制降低了他们的发展能力。在这项研究中,我们研究了体外条件如何影响大鼠植入前胚胎,这可能解释了这种能力的降低。综合基因表达分析表明,与体内发育的胚胎相比,长期体外培养的大鼠胚胎中与细胞凋亡和能量代谢相关的基因表达存在差异。此外,我们发现,与体内发育的胚胎相比,负责线粒体外膜通透性的Bak1和Bax的表达在体外培养的胚胎中更为上调。类似地,细胞凋亡依赖性DNA断裂在体外培养条件下也加剧。最后,使用CRISPR/Cas9的基因破坏表明,Bax而不是Bak1对这些效应负责。这些发现表明,长期体外培养通过线粒体途径诱导Bax依赖性细胞凋亡,并可能为改善大鼠植入前胚胎的长期培养提供线索,用于基因工程研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term culture induces Bax-dependent apoptosis in rat preimplantation embryos

Although rat preimplantation embryos are necessary for producing genetically modified rats, their in vitro culture remains a challenge. Rat zygotes can develop from the one-cell stage to the blastocyst stage in vitro; however, long-term culture reduces their developmental competence via an unknown mechanism. In this study, we examined how in vitro conditions affect rat preimplantation embryos, which may explain this reduced competence. Comprehensive gene expression analysis showed that genes related to apoptosis and energy metabolism were differentially expressed in rat embryos cultured long-term in vitro compared with those developed in vivo. Furthermore, we found that the expression of Bak1 and Bax, which are responsible for mitochondrial outer membrane permeabilization, were more upregulated in embryos cultured in vitro than those developed in vivo. Similarly, apoptosis-dependent DNA fragmentation was also exacerbated in in vitro culture conditions. Finally, gene disruption using CRISPR/Cas9 showed that Bax, but not Bak1, was responsible for these effects. These findings suggest that long-term in vitro culture induces Bax-dependent apoptosis through the mitochondrial pathway and may provide clues to improve the long-term culture of rat preimplantation embryos for genetic engineering research.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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