In Vivo Labeling by CD73 Marks Multipotent Stromal Cells and Highlights Endothelial Heterogeneity in the Bone Marrow Niche.

Breitbach, Martin; Kimura, Kenichi; Luis, Tiago C; Fuegemann, Christopher J; Woll, Petter S; Hesse, Michael; Facchini, Raffaella; Rieck, Sarah et al. · Cell Stem Cell · 2018

basic_science · Level V

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Abstract

Despite much work studying ex vivo multipotent stromal cells (MSCs), the identity and characteristics of MSCs in vivo are not well defined. Here, we generated a CD73-EGFP reporter mouse to address these questions and found EGFP<sup>+</sup> MSCs in various organs. In vivo, EGFP<sup>+</sup> mesenchymal cells were observed in fetal and adult bones at proliferative ossification sites, while in solid organs EGFP<sup>+</sup> cells exhibited a perivascular distribution pattern. EGFP<sup>+</sup> cells from the bone compartment could be clonally expanded ex vivo from single cells and displayed trilineage differentiation potential. Moreover, in the central bone marrow CD73-EGFP<sup>+</sup> specifically labeled sinusoidal endothelial cells, thought to be a critical component of the hematopoietic stem cell niche. Purification and molecular characterization of this CD73-EGFP<sup>+</sup> population revealed an endothelial subtype that also displays a mesenchymal signature, highlighting endothelial cell heterogeneity in the marrow. Thus, the CD73-EGFP mouse is a powerful tool for studying MSCs and sinusoidal endothelium.

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