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BMI1 可使人类多能干细胞具有种间嵌合性。

BMI1 enables interspecies chimerism with human pluripotent stem cells.

机构信息

Key Laboratory of Regenerative Biology of Chinese Academy of Sciences, Joint School of Life Sciences, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou Medical University, 510530, Guangzhou, China.

Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, South China Institute for Stem Cell Biology and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, 510530, Guangzhou, China.

出版信息

Nat Commun. 2018 Nov 7;9(1):4649. doi: 10.1038/s41467-018-07098-w.

Abstract

Human pluripotent stem cells (hPSCs) exhibit very limited contribution to interspecies chimeras. One explanation is that the conventional hPSCs are in a primed state and so unable  to form chimeras in pre-implantation embryos. Here, we show that the conventional hPSCs undergo rapid apoptosis when injected into mouse pre-implantation embryos. While, forced-expression of BMI1, a polycomb factor in hPSCs overcomes the apoptosis and enables hPSCs to integrate into mouse pre-implantation embryos and subsequently contribute to chimeras with both embryonic and extra-embryonic tissues. In addition, BMI1 also enables hPSCs to integrate into pre-implantation embryos of other species, such as rabbit and pig. Notably, BMI1 high expression and anti-apoptosis are also indicators for naïve hPSCs to form chimera in mouse embryos. Together, our findings reveal that the apoptosis is an initial barrier in interspecies chimerism using hPSCs and provide a rational to improve it.

摘要

人类多能干细胞(hPSCs)在种间嵌合体中表现出非常有限的贡献。一种解释是,传统的 hPSCs 处于初始状态,因此无法在植入前胚胎中形成嵌合体。在这里,我们表明,当将传统的 hPSCs 注射到小鼠植入前胚胎中时,它们会迅速凋亡。然而,在 hPSCs 中强制表达多梳抑制因子 BMI1 可克服凋亡,并使 hPSCs 整合到小鼠植入前胚胎中,并随后有助于形成具有胚胎和胚胎外组织的嵌合体。此外,BMI1 还使 hPSCs 能够整合到其他物种的植入前胚胎中,例如兔子和猪。值得注意的是,BMI1 的高表达和抗凋亡也是 hPSCs 在小鼠胚胎中形成嵌合体的原始指标。总之,我们的研究结果表明,凋亡是使用 hPSCs 进行种间嵌合体的初始障碍,并为改善它提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23a3/6220315/263eeb60d02e/41467_2018_7098_Fig1_HTML.jpg

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