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Blood vessels in the mammalian skeletal system control bone formation and support haematopoiesis by generating local niche environments. While a specialized capillary subtype, termed type H, has been recently shown to couple angiogenesis and osteogenesis in adolescent, adult and ageing mice, little is known about the formation of specific endothelial cell populations during early developmental endochondral bone formation. Here, we report that embryonic and early postnatal long bone contains a specialized endothelial cell subtype, termed type E, which strongly supports osteoblast lineage cells and later gives rise to other endothelial cell subpopulations. The differentiation and functional properties of bone endothelial cells require cell-matrix signalling interactions. Loss of endothelial integrin β1 leads to endothelial cell differentiation defects and impaired postnatal bone growth, which is, in part, phenocopied by endothelial cell-specific laminin α5 mutants. Our work outlines fundamental principles of vessel formation and endothelial cell differentiation in the developing skeletal system.

Original publication




Journal article


Nat Cell Biol

Publication Date





189 - 201


Adipokines, Animals, Apelin, Bone and Bones, Capillaries, Cell Adhesion, Endothelial Cells, Extracellular Matrix, Flow Cytometry, Immunohistochemistry, Integrases, Integrin beta1, Intercellular Signaling Peptides and Proteins, Mice, Inbred C57BL, Mice, Mutant Strains, Neovascularization, Physiologic, Osteogenesis, Phenotype, Signal Transduction, X-Ray Microtomography