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诱导多能干细胞中 X 染色体失活状态受分化条件影响。

Derivation conditions impact X-inactivation status in female human induced pluripotent stem cells.

机构信息

Gladstone Institute of Cardiovascular Disease, University of California, San Francisco, San Francisco, CA 94158, USA.

出版信息

Cell Stem Cell. 2012 Jul 6;11(1):91-9. doi: 10.1016/j.stem.2012.05.019.

Abstract

Female human induced pluripotent stem cell (hiPSC) lines exhibit variability in X-inactivation status. The majority of hiPSC lines maintain one transcriptionally active X (Xa) and one inactive X (Xi) chromosome from donor cells. However, at low frequency, hiPSC lines with two Xas are produced, suggesting that epigenetic alterations of the Xi occur sporadically during reprogramming. We show here that X-inactivation status in female hiPSC lines depends on derivation conditions. hiPSC lines generated by the Kyoto method (retroviral or episomal reprogramming), which uses leukemia inhibitory factor (LIF)-expressing SNL feeders, frequently had two Xas. Early passage Xa/Xi hiPSC lines generated on non-SNL feeders were converted into Xa/Xa hiPSC lines after several passages on SNL feeders, and supplementation with recombinant LIF caused reactivation of some of X-linked genes. Thus, feeders are a significant factor affecting X-inactivation status. The efficient production of Xa/Xa hiPSC lines provides unprecedented opportunities to understand human X-reactivation and -inactivation.

摘要

女性人类诱导多能干细胞(hiPSC)系表现出 X 染色体失活状态的可变性。大多数 hiPSC 系从供体细胞中维持一条转录活跃的 X(Xa)和一条失活的 X(Xi)染色体。然而,在低频下,产生了两条 Xa 的 hiPSC 系,这表明在重编程过程中 Xi 的表观遗传改变偶尔发生。我们在这里表明,雌性 hiPSC 系的 X 染色体失活状态取决于衍生条件。使用白血病抑制因子(LIF)表达 SNL 饲养细胞的京都方法(逆转录病毒或 episomal 重编程)产生的 hiPSC 系,通常具有两条 Xa。在非 SNL 饲养细胞上生成的早期传代 Xa / Xi hiPSC 系在几轮 SNL 饲养细胞上后转化为 Xa / Xa hiPSC 系,并且补充重组 LIF 导致一些 X 连锁基因的重新激活。因此,饲养细胞是影响 X 染色体失活状态的重要因素。Xa / Xa hiPSC 系的高效产生提供了前所未有的机会来理解人类 X 染色体的激活和失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5315/3396435/1419519f53f8/nihms-379457-f0001.jpg

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