Douglas Mortlock
Assistant Professor of Molecular Physiology & Biop
Last active: 8/21/2016

Skeletal trauma generates systemic BMP2 activation that is temporally related to the mobilization of CD73+ cells.

Marsell R, Steen B, Bais MV, Mortlock DP, Einhorn TA, Gerstenfeld LC
J Orthop Res. 2014 32 (1): 17-23

PMID: 24018651 · PMCID: PMC4263190 · DOI:10.1002/jor.22487

The relationship between BMP2 expression and the recruitment of skeletogenic stem cells was assessed following bone marrow reaming. BMP2 expression was examined using transgenic mice in which β-galactosidase had been inserted into the coding region of BMP2. Stem cell mobilization was analyzed by FACS analysis using CD73, a marker associated with bone marrow stromal stem cells. BMP2 expression was induced in endosteal lining cells, cortical osteocytes and periosteal cells in both the reamed and in contralateral bones. BMP2 mRNA expression in the reamed bone showed an early peak within the first 24 h of reaming followed by a later peak at 7 days, while contralateral bones only showed the 7 days peak of expression. FACS analysis sorting on CD73 positive cells showed a 50% increase of these cells at 3 and 14 days in the marrow of the injured bone and a single peak at 14 days of the marrow cell population of the contralateral bone. A ∼20% increase of CD73 positive cells was seen in the peripheral blood 2 days after reaming. These data showed that traumatic bone injury caused a systemic induction of BMP2 expression and that this increase is correlated with the mobilization of CD73 positive cells.

© 2013 The Authors. Journal of Orthopaedic Research Published by Wiley Periodicals, Inc. on behalf of the Orthopaedic Research Society.

MeSH Terms (17)

5'-Nucleotidase Animals Bone Marrow Cells Bone Morphogenetic Protein 2 Cells, Cultured Chemokine CXCL12 Disease Models, Animal Flow Cytometry Hematopoietic Stem Cell Mobilization Mesenchymal Stem Cells Mice Mice, Inbred C57BL Mice, Transgenic Osteogenesis Receptors, CXCR4 Stromal Cells Tibia

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