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用三种抑制剂重编程的诱导多能干细胞表现出加速分化潜能,具有高水平的 2 细胞期标志物表达。

Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression.

机构信息

Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

Center for Genomic and Regenerative Medicine, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.

出版信息

Stem Cell Reports. 2019 Feb 12;12(2):305-318. doi: 10.1016/j.stemcr.2018.12.018. Epub 2019 Jan 31.

DOI:10.1016/j.stemcr.2018.12.018
PMID:30713040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6373546/
Abstract

Although pluripotent stem cells can generate various types of differentiated cells, it is unclear why lineage-committed stem/progenitor cells derived from pluripotent stem cells are decelerated and why the differentiation-resistant propensity of embryonic stem cell (ESC)/induced pluripotent stem cell (iPSC)-derived cells is predominant compared with the in vivo equivalents derived from embryonic/adult tissues. In this study, we demonstrated that iPSCs reprogrammed and maintained with three chemical inhibitors of the fibroblast growth factor 4-mitogen-activated protein kinase cascade and GSK3β (3i) could be differentiated into all three germ layers more efficiently than the iPSCs reprogrammed without the 3i chemicals, even though they were maintained with 3i chemicals once they were reprogrammed. Although the iPSCs reprogrammed with 3i had increased numbers of Zscan4-positive cells, the Zscan4-positive cells among iPSCs that were reprogrammed without 3i did not have an accelerated differentiation ability. These observations suggest that 3i exposure during the reprogramming period determines the accelerated differentiation/maturation potentials of iPSCs that are stably maintained at the distinct state.

摘要

虽然多能干细胞可以产生各种类型的分化细胞,但尚不清楚为什么来自多能干细胞的谱系定向干细胞/祖细胞会减速,以及为什么胚胎干细胞 (ESC)/诱导多能干细胞 (iPSC) 衍生细胞的分化抗性倾向比源自胚胎/成人组织的体内等同物更为明显。在这项研究中,我们证明了使用三种成纤维细胞生长因子 4-有丝分裂原激活蛋白激酶级联和 GSK3β 的化学抑制剂(3i)重新编程和维持的 iPSC 比未使用 3i 化学物质重新编程的 iPSC 更有效地分化为所有三个胚层,即使它们在重新编程后也使用 3i 化学物质维持。尽管使用 3i 重新编程的 iPSC 中 Zscan4 阳性细胞的数量增加了,但未使用 3i 重新编程的 iPSC 中的 Zscan4 阳性细胞并没有加速分化能力。这些观察结果表明,在重新编程期间暴露于 3i 决定了 iPSC 的加速分化/成熟潜力,这些 iPSC 在不同状态下稳定维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/5bbcdb856f96/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/371d2f3703c1/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/173405f2075f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/ea272b884b15/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/f7496a6cb949/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/5bbcdb856f96/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/371d2f3703c1/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/173405f2075f/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/ea272b884b15/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/f7496a6cb949/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedb/6373546/5bbcdb856f96/gr4.jpg

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