Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Stem Cell Rev Rep. 2021 Dec;17(6):2304-2313. doi: 10.1007/s12015-021-10253-4. Epub 2021 Sep 24.
Polycomb group protein Bmi1 is essential for hematopoietic stem cell (HSC) self-renewal and terminal differentiation. However, its target genes in hematopoietic stem and progenitor cells are largely unknown. We performed gene expression profiling assays and found that genes of the Wnt signaling pathway are significantly elevated in Bmi1 null hematopoietic stem and progenitor cells (HSPCs). Bmi1 is associated with several genes of the Wnt signaling pathway in hematopoietic cells. Further, we found that Bmi1 represses Wnt gene expression in HSPCs. Importantly, loss of β-catenin, which reduces Wnt activation, partially rescues the HSC self-renewal and differentiation defects seen in the Bmi1 null mice. Thus, we have identified Bmi1 as a novel regulator of Wnt signaling pathway in HSPCs. Given that Wnt signaling pathway plays an important role in hematopoiesis, our studies suggest that modulating Wnt signaling may hold potential for enhancing HSC self-renewal, thereby improving the outcomes of HSC transplantation.
多梳抑制复合物蛋白 Bmi1 对于造血干细胞(HSC)自我更新和终末分化是必需的。然而,其在造血干细胞和祖细胞中的靶基因在很大程度上是未知的。我们进行了基因表达谱分析实验,发现 Bmi1 缺失的造血干细胞和祖细胞(HSPCs)中 Wnt 信号通路的基因显著上调。Bmi1 与造血细胞中 Wnt 信号通路的几个基因相关。此外,我们发现 Bmi1 在 HSPCs 中抑制 Wnt 基因的表达。重要的是,β-连环蛋白(β-catenin)的缺失(降低了 Wnt 的激活)部分挽救了 Bmi1 缺失小鼠中观察到的 HSC 自我更新和分化缺陷。因此,我们已经确定 Bmi1 是 HSPCs 中 Wnt 信号通路的一个新的调节因子。鉴于 Wnt 信号通路在造血中起着重要作用,我们的研究表明,调节 Wnt 信号可能具有增强 HSC 自我更新的潜力,从而改善 HSC 移植的结果。