The Wnt5a Receptor, Receptor Tyrosine Kinase-Like Orphan Receptor 2, Is a Predictive Cell Surface Marker of Human Mesenchymal Stem Cells with an Enhanced Capacity for Chondrogenic Differentiation

• DOI: 10.1002/stem.2691
• Publication Date: 2017-08-21T04:52:51Z
• Authors: Sally C. Dickinson; Catherine A. Sutton; Kyla Brady; Anna Salerno; Theoni Katopodi; Rhys L. Williams; Christopher C. West; Denis Evseenko; Ling Wu; Suzanna Pang; Roberta Ferro de ...; Allen E. Goodship; Bruno Péault; Ashley W. Blom; Wael Kafienah; Anthony P. Hollander
• Keywords: 0303 health sciences; Sheep; Tissue Engineering; Cellular therapy; 610; Cell Differentiation; Mesenchymal Stem Cells; /dk/atira/pure/core/keywords/centre_for_surgical_research; name=Centre for Surgical Research; TISSUE ENGINEERING; Receptor Tyrosine Kinase-like Orphan Receptors; Wnt-5a Protein; Tissue‐Specific Stem Cells; 03 medical and health sciences; Cell Signaling; Journal Article; Mesenchymal stem cells; Animals; Humans; name=Centre for Surgical Research; ARTHRITIS; /dk/atira/pure/core/keywords/centre_for_surgical_research; Chondrogenesis; Cells, Cultured; Cell Proliferation

AbstractMultipotent mesenchymal stem cells (MSCs) have enormous potential in tissue engineering and regenerative medicine. However, until now, their development for clinical use has been severely limited as they are a mixed population of cells with varying capacities for lineage differentiation and tissue formation. Here, we identify receptor tyrosine kinase-like orphan receptor 2 (ROR2) as a cell surface marker expressed by those MSCs with an enhanced capacity for cartilage formation. We generated clonal human MSC populations with varying capacities for chondrogenesis. ROR2 was identified through screening for upregulated genes in the most chondrogenic clones. When isolated from uncloned populations, ROR2+ve MSCs were significantly more chondrogenic than either ROR2–ve or unfractionated MSCs. In a sheep cartilage-repair model, they produced significantly more defect filling with no loss of cartilage quality compared with controls. ROR2+ve MSCs/perivascular cells were present in developing human cartilage, adult bone marrow, and adipose tissue. Their frequency in bone marrow was significantly lower in patients with osteoarthritis (OA) than in controls. However, after isolation of these cells and their initial expansion in vitro, there was greater ROR2 expression in the population derived from OA patients compared with controls. Furthermore, osteoarthritis-derived MSCs were better able to form cartilage than MSCs from control patients in a tissue engineering assay. We conclude that MSCs expressing high levels of ROR2 provide a defined population capable of predictably enhanced cartilage production.