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使用 t5iLA 幼稚态人多能干细胞进行 X 染色体失活建模。

Modeling X chromosome inactivation using t5iLA naive human pluripotent stem cells.

机构信息

Department of Obstetrics and Gynecology, Guangdong Provincial Key Laboratory for Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine, The Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

出版信息

BMC Biol. 2024 Sep 18;22(1):210. doi: 10.1186/s12915-024-01994-y.

Abstract

BACKGROUND

X chromosome inactivation (XCI) is a critical epigenetic event for dosage compensation of X-linked genes in female mammals, ensuring developmental stability. A robust in vitro model is required for mimicking XCI during the early stages of embryonic development. This methodology article introduces an advanced framework for the in-depth study of XCI using human pluripotent stem cells (hPSCs). By focusing on the transition between naive and primed pluripotent states, we highlight the role of long non-coding RNA X-inactive specific transcript (XIST) and epigenetic alterations in mediating XCI.

RESULTS

Our methodology enables the distinction between naive and primed hESCs based on XIST expression and the activity of X-linked reporters, facilitating the investigation of XCI initiation and maintenance. Through detailed experimental procedures, we demonstrate the utility of our hESC lines in modeling the process of human XCI, including the establishment of conditions for random XCI induction and the analysis of X chromosome reactivation.

METHODS

The study outlines a comprehensive approach for characterizing the X chromosome status in hPSCs, employing dual fluorescent reporter hESC lines. These reporter lines enable real-time tracking of XCI dynamics through differentiation processes. We detailed protocols for the induction of X chromosome reactivation and inactivation, as well as the X status characterization methods including cultivation of hESCs, flow cytometric analysis, RNA fluorescence in situ hybridization (FISH), and transcriptome sequencing, providing a step-by-step guide for researchers to investigate XCI mechanisms in vitro.

CONCLUSIONS

This article provides a detailed, reproducible methodology for studying XCI mechanisms in vitro, employing hPSCs as a model system. It presents a significant advance in our ability to investigate XCI, offering potential applications in developmental biology, disease modeling, and regenerative medicine. By facilitating the study of XCI dynamics, this methodological framework paves the way for deeper understanding and manipulation of this fundamental biological process.

摘要

背景

X 染色体失活(XCI)是雌性哺乳动物中 X 连锁基因剂量补偿的关键表观遗传事件,确保了发育的稳定性。需要建立一个稳健的体外模型来模拟胚胎发育早期的 XCI。本文方法介绍了一种使用人类多能干细胞(hPSC)深入研究 XCI 的先进框架。通过关注原始和初始多能状态之间的转变,我们强调了长非编码 RNA X 失活特异性转录物(XIST)和表观遗传改变在介导 XCI 中的作用。

结果

我们的方法基于 XIST 表达和 X 连锁报告基因的活性,能够区分原始和初始 hESC,从而促进了对 XCI 起始和维持的研究。通过详细的实验程序,我们展示了我们的 hESC 系在模拟人类 XCI 过程中的应用,包括建立随机 XCI 诱导的条件和分析 X 染色体重新激活。

方法

本研究概述了一种全面的方法,用于通过使用双荧光报告 hESC 系来描述 hPSC 中 X 染色体的状态。这些报告系通过分化过程实时跟踪 XCI 动力学。我们详细介绍了诱导 X 染色体重新激活和失活的方案,以及 X 状态特征方法,包括 hESC 的培养、流式细胞分析、RNA 荧光原位杂交(FISH)和转录组测序,为研究人员提供了一个体外研究 XCI 机制的分步指南。

结论

本文提供了一种详细、可重复的方法,用于在体外研究 XCI 机制,使用 hPSC 作为模型系统。它代表了我们在研究 XCI 方面的能力的重大进步,为发育生物学、疾病建模和再生医学提供了潜在的应用。通过促进 XCI 动力学的研究,这个方法框架为更深入地理解和操纵这个基本的生物学过程铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1700/11411763/cbad24c89174/12915_2024_1994_Fig1_HTML.jpg

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