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染色质重塑复合物 CHD1 调控间充质基质细胞的原始状态以控制其干细胞支持活性。

The Chromatin Remodeling Complex CHD1 Regulates the Primitive State of Mesenchymal Stromal Cells to Control Their Stem Cell Supporting Activity.

机构信息

Catholic High-Performance Cell Therapy Center, The Catholic University of Korea, Seoul, Republic of Korea.

出版信息

Stem Cells Dev. 2021 Apr 1;30(7):363-373. doi: 10.1089/scd.2020.0166.

Abstract

The primitive state (stemness) of mesenchymal stromal cells (MSCs) is responsible for supporting the function of tissue-specific stem cells to regenerate damaged tissues. However, molecular mechanisms regulating the stemness of MSCs remain unknown. In this study, we found that the primitive state of MSCs is hierarchically regulated by the expression levels of the chromatin remodeling complex, CHD1, with CHD1 expression levels higher in the undifferentiated state, and decreasing upon MSC differentiation. Consistently, CHD1 expression levels decrease during progressive loss of clonogenic progenitors (CFU-F) induced by passage cultures. Moreover, knockdown (KD) of CHD1 decreased CFU-F frequency, whereas CHD1 overexpression increased it. In addition, the expression of stem cell-specific genes was down- or upregulated upon KD or overexpression of CHD1, respectively, accompanied by associated changes in chromatin condensation. Importantly, altering CHD1 expression levels affected the ability of MSCs to support the self-renewing expansion of hematopoietic stem cells (HSCs). Furthermore, CHD1 levels were significantly decreased in MSCs from acute myeloid leukemia or aplastic anemia patients, where CFU-F and HSC-supporting activities are lost. Altogether, these findings show that chromatin remodeling by CHD1 is a molecular parameter that influences the primitive state of MSCs and their stem cell-supporting activity, which controls tissue regeneration.

摘要

间充质基质细胞 (MSCs) 的原始状态(干性)负责支持组织特异性干细胞再生受损组织的功能。然而,调节 MSCs 干性的分子机制尚不清楚。在这项研究中,我们发现 MSCs 的原始状态是由染色质重塑复合物 CHD1 的表达水平分层调节的,在未分化状态下 CHD1 的表达水平较高,而在 MSC 分化时则降低。一致地,CHD1 的表达水平在传代培养诱导的克隆形成祖细胞(CFU-F)逐渐丧失过程中降低。此外,CHD1 的敲低 (KD) 降低了 CFU-F 的频率,而 CHD1 的过表达则增加了它。此外,CHD1 的敲低或过表达分别下调或上调了干细胞特异性基因的表达,伴随着染色质凝聚的相关变化。重要的是,改变 CHD1 的表达水平会影响 MSCs 支持造血干细胞 (HSCs) 自我更新扩增的能力。此外,在急性髓系白血病或再生障碍性贫血患者的 MSCs 中,CHD1 水平显著降低,CFU-F 和 HSC 支持活性丧失。总之,这些发现表明 CHD1 介导的染色质重塑是影响 MSCs 原始状态及其支持干细胞活性的分子参数,而后者控制着组织再生。

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