Objective
Previous genetic lineage tracing studies showed that Sox10+ cells differentiate into vascular mural cells, limited to neural crest-derived blood vessels in craniofacial tissues, aortic arch, pulmonary arch arteries, brachiocephalic, carotid arteries and thymus. The purpose of this study was to investigate the contribution of Sox10+ cells to the vascular development in other tissues and organs and their relationship with neural crest.
Approach and Results
Using genetic lineage tracing technique based on Cre/LoxP system, we examined blood vessels of the adult organs of Sox10-Cre/Rosa-LoxP-RFP and Wnt1-Cre/Rosa-LoxP-RFP mice by immunohistological analysis. In addition to previously reported tissues and organs derived from neural crest, we showed that Sox10+ cells also contributed to vascular mural cells in the lung, spleen and kidney, which are derived from non-neural crest origin as evidenced by RFP- blood vessels in these three organs of Wnt1-Cre/Rosa-LoxP-RFP mice.
Conclusions
This study demonstrates that Sox10+ cells contribute to pericytes and smooth muscle cells in most parts of the body, including those from both neural crest and non-neural crest, which has significant implications in vascular remodeling under physiological and pathological conditions.