Department of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Physics Department, Ben Gurion University of the Negev, Beer-Sheva 84105, Israel.
Cell Stem Cell. 2020 Aug 6;27(2):336-345.e4. doi: 10.1016/j.stem.2020.06.003. Epub 2020 Jun 25.
Adult mammalian hematopoietic stem cells (HSCs) reside in the bone marrow (BM) but can be mobilized into blood for use in transplantation. HSCs interact with BM niche cells that produce growth factor c-Kit ligand (Kitl/SCF) and chemokine CXCL12, and were thought to be static and sessile. We used two-photon laser scanning microscopy to visualize genetically labeled HSCs in the BM of live mice for several hours. The majority of HSCs showed a dynamic non-spherical morphology and significant motility, undergoing slow processive motion interrupted by short stretches of confined motion. HSCs moved in the perivascular space and showed intermittent close contacts with SCF-expressing perivascular stromal cells. In contrast, mobilization-inducing blockade of CXCL12 receptor CXCR4 and integrins rapidly abrogated HSC motility and shape dynamics in real time. Our results reveal an unexpectedly dynamic nature of HSC residence in the BM and interaction with the SCF stromal niche, which is disrupted during HSC mobilization.
成体哺乳动物造血干细胞(HSCs)存在于骨髓(BM)中,但可以动员到血液中用于移植。HSCs 与产生生长因子 c-Kit 配体(Kitl/SCF)和趋化因子 CXCL12 的 BM 生态位细胞相互作用,被认为是静止和固着的。我们使用双光子激光扫描显微镜在活小鼠的 BM 中可视化遗传标记的 HSCs 数小时。大多数 HSCs 表现出动态的非球形形态和显著的运动性,经历缓慢的连续运动,被短暂的受限运动打断。HSCs 在血管周围空间中移动,并显示与表达 SCF 的血管周围基质细胞间歇性的紧密接触。相比之下,动员诱导的 CXCL12 受体 CXCR4 和整合素阻断迅速实时消除 HSC 的运动性和形态动力学。我们的结果揭示了 HSC 在 BM 中的驻留和与 SCF 基质生态位相互作用的出乎意料的动态性质,在 HSC 动员过程中这种相互作用被破坏。