Passaro Diana, Abarrategi Ander, Foster Katie, Ariza-McNaughton Linda, Bonnet Dominique
Haematopoietic Stem Cell Laboratory, The Francis Crick Institute.
Haematopoietic Stem Cell Laboratory, The Francis Crick Institute;
J Vis Exp. 2017 Aug 1(126):55914. doi: 10.3791/55914.
Human hematopoietic stem cells (HSCs) reside in the bone marrow (BM) niche, an intricate, multifactorial network of components producing cytokines, growth factors, and extracellular matrix. The ability of HSCs to remain quiescent, self-renew or differentiate, and acquire mutations and become malignant depends upon the complex interactions they establish with different stromal components. To observe the crosstalk between human HSCs and the human BM niche in physiological and pathological conditions, we designed a protocol to ectopically model and image a humanized BM niche in immunodeficient mice. We show that the use of different cellular components allows for the formation of humanized structures and the opportunity to sustain long-term human hematopoietic engraftment. Using two-photon microscopy, we can live-image these structures in situ at the single-cell resolution, providing a powerful new tool for the functional characterization of the human BM microenvironment and its role in regulating normal and malignant hematopoiesis.
人类造血干细胞(HSCs)存在于骨髓(BM)微环境中,这是一个由产生细胞因子、生长因子和细胞外基质的成分组成的复杂多因素网络。造血干细胞保持静止、自我更新或分化、获得突变并发生恶变的能力取决于它们与不同基质成分建立的复杂相互作用。为了观察生理和病理条件下人类造血干细胞与人类骨髓微环境之间的相互作用,我们设计了一个方案,在免疫缺陷小鼠中异位模拟和成像人源化骨髓微环境。我们表明,使用不同的细胞成分可以形成人源化结构,并为长期维持人类造血植入提供机会。利用双光子显微镜,我们可以在单细胞分辨率下对这些结构进行原位实时成像,为人类骨髓微环境的功能表征及其在调节正常和恶性造血中的作用提供了一个强大的新工具。