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Lrp5 和 Lrp6 对于维持造血干细胞的自我更新和分化是必需的。

Lrp5 and Lrp6 are required for maintaining self-renewal and differentiation of hematopoietic stem cells.

机构信息

State Key Laboratory of Agrobiotechnology and, China Agricultural University, Beijing, China.

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Biological Sciences, China Agricultural University, Beijing, China; and.

出版信息

FASEB J. 2019 Apr;33(4):5615-5625. doi: 10.1096/fj.201802072R. Epub 2019 Jan 22.

Abstract

Hematopoietic stem cells (HSCs) have the capacity for self-renewal to maintain the HSCs' pool and the ability for multilineage differentiation, which are responsible for sustained production of multiple blood lineages. The regulation of HSC development is controlled precisely by complex signal networks and hematopoietic microenvironment, which has been termed the HSCs' niche. The Wnt signaling pathway is one of a variety of signaling pathways that have been involved in HSC self-renewal and maintenance. Previous studies are indeterminant on the regulation of adult HSCs upon canonical Wnt signaling pathways because of the different experimental systems and models used. In this study, we generated the conditional knockout Wnt coreceptor low-density lipoprotein receptor-related protein 5 (Lrp5) and low-density lipoprotein receptor-related protein 6 (Lrp6) mice in adult hematopoiesis via Vav-Cre Loxp system. Inactivation of Lrp5 and -6 in a hematopoietic system diminished the pool of HSCs, but there were no obvious defects in mature immune cells. Lrp5 and -6 double deficiency HSCs showed intrinsic defects in self-renewal and differentiation due to reduced proliferation and increased quiescence of the cell cycle. Analysis of HSC gene expression suggested that the quiescence regulators were significantly up-regulated, such as Egr1, Cdkn1a, Nr4a1, Gata2, Junb and Btg2, and the positive cell cycle regulators were correspondingly down-regulated, such as Ccna2 and Ranbp1. Taken together, we investigated the roles of Lrp5 and -6 in HSCs by functional and bioinformatic assays, and we demonstrated that Lrp5 and -6 are required for the self-renewal and differentiation of adult HSCs. The canonical Wnt pathway may contribute to maintaining the HSC pool and regulate the differentiation of adult HSCs by controlling cell cycle gene regulatory module.-Liu, J., Cui, Z., Wang, F., Yao, Y., Yu, G., Liu, J., Cao, D., Niu, S., You, M., Sun, Z., Lian, D., Zhao, T., Kang, Y., Zhao, Y., Xue, H.-H., Yu, S. Lrp5 and Lrp6 are required for maintaining self-renewal and differentiation of hematopoietic stem cells.

摘要

造血干细胞(HSCs)具有自我更新的能力,以维持 HSCs 池,并具有多谱系分化的能力,这是维持多种血液谱系持续产生的原因。HSC 发育的调节受复杂的信号网络和造血微环境的精确控制,这被称为 HSCs 的龛位。Wnt 信号通路是参与 HSC 自我更新和维持的多种信号通路之一。由于使用了不同的实验系统和模型,以前的研究对于经典 Wnt 信号通路对成体 HSCs 的调节是不确定的。在这项研究中,我们通过 Vav-Cre Loxp 系统在成体造血中生成了条件性敲除 Wnt 共受体低密度脂蛋白受体相关蛋白 5(Lrp5)和低密度脂蛋白受体相关蛋白 6(Lrp6)的小鼠。造血系统中 Lrp5 和 -6 的失活减少了 HSCs 池,但成熟免疫细胞没有明显缺陷。Lrp5 和 -6 双缺失 HSCs 由于细胞周期增殖减少和静止增加,表现出自我更新和分化的内在缺陷。HSC 基因表达分析表明,静止调节因子显著上调,如 Egr1、Cdkn1a、Nr4a1、Gata2、Junb 和 Btg2,而阳性细胞周期调节因子相应地下调,如 Ccna2 和 Ranbp1。总之,我们通过功能和生物信息学分析研究了 Lrp5 和 -6 在 HSCs 中的作用,并证明 Lrp5 和 -6 是成体 HSCs 自我更新和分化所必需的。经典 Wnt 途径可能通过控制细胞周期基因调控模块,有助于维持 HSC 池并调节成体 HSCs 的分化。-刘,J.,崔,Z.,王,F.,姚,Y.,于,G.,刘,J.,曹,D.,牛,S.,尤,M.,孙,Z.,连,D.,赵,T.,康,Y.,赵,Y.,薛,H.-H.,于,S. Lrp5 和 Lrp6 是维持造血干细胞自我更新和分化所必需的。

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