Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400030, China.
Cell Mol Life Sci. 2022 Jul 6;79(8):399. doi: 10.1007/s00018-022-04411-1.
Hematopoietic stem/progenitor cells (HSPCs) originate from endothelial cells (ECs) localized on the ventral side of the dorsal aorta (DA), and hemodynamic parameters may suffer sharp changes in DA at HSPCs development stage for intersegmental vessel formation. However, the temporal-spatial shear stress parameters and biomechanics mechanisms of HSPC budding remain unknown. Here, we found that the hematopoietic endothelium (HE) in the aorta-gonad-mesonephros was heterogeneous; that is, HEs were mainly distributed at the ventral side of the vascular bifurcation in zebrafish embryos, which was found to show low shear stress (LSS) through numerical simulation analysis. Furthermore, HSPCs localized in the posterior somite of aorta-gonad-mesonephros with slow velocity. On the temporal scale, there was a slow velocity and LSS during HE budding from 36 h post-fertilization and decreased shear stress with drug expanded HSPC numbers. Mechanistically, matrix metalloproteinase (MMP) expression and macrophage chemotaxis were significantly increased in HEs by RNA-seq. After treatment with an MMP13 inhibitor, HSPCs were significantly reduced in both the aorta-gonad-mesonephros and caudal hematopoietic tissue in embryos. Our results show that HSPC budding is heterogeneous, and the mechanism is that physiological LSS controls the emergence of HSPCs by promoting the accumulation of macrophages and subsequent MMP expression.
造血干/祖细胞 (HSPCs) 起源于位于背主动脉 (DA) 腹侧的内皮细胞 (ECs),并且在 HSPCs 发育阶段,用于节间血管形成的血流动力学参数可能会发生急剧变化。然而,HSPC 出芽的时空调速剪切力参数和生物力学机制尚不清楚。在这里,我们发现主动脉-性腺-中肾的造血内皮 (HE) 是异质的;即 HE 主要分布在斑马鱼胚胎血管分叉的腹侧,通过数值模拟分析发现其具有低剪切应力 (LSS)。此外,HSPC 定位于主动脉-性腺-中肾的后体节,流速较慢。在时间尺度上,HE 从受精后 36 小时开始出芽时具有较慢的速度和 LSS,并且随着药物的作用,剪切应力减小,HSPC 数量增加。从机制上讲,通过 RNA-seq 发现 HE 中的基质金属蛋白酶 (MMP) 表达和巨噬细胞趋化性显著增加。在用 MMP13 抑制剂处理后,胚胎中的主动脉-性腺-中肾和尾造血组织中的 HSPCs 数量明显减少。我们的研究结果表明,HSPC 出芽是异质的,其机制是生理 LSS 通过促进巨噬细胞的积累和随后的 MMP 表达来控制 HSPCs 的出现。