| Literature DB >> 29451855 |
Martin Breitbach1, Kenichi Kimura2, Tiago C Luis3, Christopher J Fuegemann4, Petter S Woll5, Michael Hesse6, Raffaella Facchini3, Sarah Rieck4, Katarzyna Jobin7, Julia Reinhardt8, Osamu Ohneda9, Daniela Wenzel4, Caroline Geisen6, Christian Kurts7, Wolfgang Kastenmüller7, Michael Hölzel8, Sten E W Jacobsen10, Bernd K Fleischmann11.
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+ 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.Entities:
Keywords: bone marrow; endothelial cell heterogeneity; multipotent stromal cells; sinusoidal endothelial cells; stem cell niche
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Year: 2018 PMID: 29451855 DOI: 10.1016/j.stem.2018.01.008
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633