| First Author | Breitbach M | Year | 2018 |
| Journal | Cell Stem Cell | Volume | 22 |
| Issue | 2 | Pages | 262-276.e7 |
| PubMed ID | 29451855 | Mgi Jnum | J:271493 |
| Mgi Id | MGI:6278054 | Doi | 10.1016/j.stem.2018.01.008 |
| Citation | Breitbach M, et al. (2018) In Vivo Labeling by CD73 Marks Multipotent Stromal Cells and Highlights Endothelial Heterogeneity in the Bone Marrow Niche. Cell Stem Cell 22(2):262-276.e7 |
| abstractText | 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(+) MSCs in various organs. In vivo, EGFP(+) mesenchymal cells were observed in fetal and adult bones at proliferative ossification sites, while in solid organs EGFP(+) cells exhibited a perivascular distribution pattern. EGFP(+) 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(+) 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(+) 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. |
