Wnt 对造血干细胞发育和疾病的调控。

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Current Topics in Developmental Biology Pub Date : 2023-01-01 Epub Date: 2023-01-09 DOI:10.1016/bs.ctdb.2022.12.001
Kelsey A Carpenter, Kate E Thurlow, Sonya E L Craig, Stephanie Grainger
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引用次数: 0

摘要

造血干细胞是一种多能干细胞,可产生所有血液细胞和大多数免疫细胞。由于造血干细胞具有无限自我更新的能力,因此在生物体的整个生命过程中,长期造血干细胞都在补充血液和免疫细胞。造血干细胞的发育、维持和分化都受到包括 Wnt 通路在内的细胞信号通路的严格调控。Wnt 信号由分泌配体在细胞外启动,配体与细胞表面受体结合,产生多个不同的下游信号级联。根据其对β-catenin转录激活因子的依赖程度,这些信号级联可分为依赖β-catenin(BCD)信号级联和独立β-catenin(BCI)信号级联。造血干细胞的发育、稳态和分化受 BCD 和 BCI 的影响,对 Wnt 信号的时间和剂量高度敏感。重要的是,Wnt 信号失调可导致血液恶性肿瘤,如白血病、淋巴瘤和骨髓瘤。在此,我们回顾了 Wnt 信号如何在造血干细胞的发育过程中和疾病发生时对其产生影响。
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Wnt regulation of hematopoietic stem cell development and disease.

Hematopoietic stem cells (HSCs) are multipotent stem cells that give rise to all cells of the blood and most immune cells. Due to their capacity for unlimited self-renewal, long-term HSCs replenish the blood and immune cells of an organism throughout its life. HSC development, maintenance, and differentiation are all tightly regulated by cell signaling pathways, including the Wnt pathway. Wnt signaling is initiated extracellularly by secreted ligands which bind to cell surface receptors and give rise to several different downstream signaling cascades. These are classically categorized either β-catenin dependent (BCD) or β-catenin independent (BCI) signaling, depending on their reliance on the β-catenin transcriptional activator. HSC development, homeostasis, and differentiation is influenced by both BCD and BCI, with a high degree of sensitivity to the timing and dosage of Wnt signaling. Importantly, dysregulated Wnt signals can result in hematological malignancies such as leukemia, lymphoma, and myeloma. Here, we review how Wnt signaling impacts HSCs during development and in disease.

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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
91
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