Medical Innovation Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Center for iPS Research and Application, Kyoto University, Kyoto, Japan.
Cancer Sci. 2019 Apr;110(4):1317-1330. doi: 10.1111/cas.13974. Epub 2019 Mar 18.
Adult long-term hematopoiesis depends on sustaining hematopoietic stem/progenitor cells (HSPC) in bone marrow (BM) niches, where their balance of quiescence, self-renewal, and hematopoietic differentiation is tightly regulated. Although various BM stroma cells that produce niche factors have been identified, regulation of the intrinsic responsiveness of HSPC to the niche factors remains elusive. We previously reported that mice deficient for Sipa1, a Rap1 GTPase-activating protein, develop diverse hematopoietic disorders of late onset. Here we showed that transplantation of BM cells expressing membrane-targeted C3G (C3G-F), a Rap1 GTP/GDP exchanger, resulted in the progressive decline of the numbers of HSPC repopulated in BM with time and impaired long-term hematopoiesis of all cell lineages. C3G-F/HSPC were sustained for months in spleen retaining hematopoietic potential, but these cells inefficiently contributed to overall hematopoietic reconstitution. C3G-F/HSPC showed enhanced proliferation and differentiation with accelerated progenitor cell exhaustion in response to stem cell factor (SCF). Using a Ba/F3 cell line, we confirmed that the increased basal Rap1GTP levels with C3G-F expression caused a markedly prolonged activation of c-Kit receptor and downstream signaling through SCF ligation. A minor population of C3G-F/HSPC also showed enhanced proliferation in the presence of thrombopoietin (TPO) compared to Vect/HSPC. Current results suggest an important role of basal Rap1 activation status of HSPC in their maintenance in BM for sustaining long-term adult hematopoiesis.
成人长期造血依赖于维持骨髓(BM)龛中的造血干细胞/祖细胞(HSPC),其静止、自我更新和造血分化的平衡受到严格调控。虽然已经鉴定出产生龛位因子的各种 BM 基质细胞,但 HSPC 对龛位因子固有反应性的调节仍不清楚。我们之前报道过,Rap1 GTPase 激活蛋白 Sipa1 缺失的小鼠会出现多种迟发性造血障碍。在这里,我们表明,表达膜靶向 C3G(C3G-F)的 BM 细胞的移植(一种 Rap1 GTP/GDP 交换蛋白)导致 HSPC 在 BM 中的重编程数量随着时间的推移逐渐减少,并损害了所有细胞谱系的长期造血。C3G-F/HSPC 在脾脏中持续存在数月,保留造血潜能,但这些细胞对整体造血重建的贡献效率低下。C3G-F/HSPC 在对干细胞因子(SCF)的反应中表现出增强的增殖和分化,以及祖细胞衰竭的加速。使用 Ba/F3 细胞系,我们证实 C3G-F 表达导致 Rap1GTP 水平的基础增加,从而显著延长了 c-Kit 受体的激活和下游信号传导通过 SCF 连接。与 Vect/HSPC 相比,C3G-F/HSPC 的一小部分也表现出在存在血小板生成素(TPO)时的增殖增强。目前的结果表明,HSPC 基础 Rap1 激活状态在维持其在 BM 中的长期成人造血中的重要作用。