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TISSUE-SPECIFIC STEM CELLS

Circulating Bone Marrow-Derived Osteoblast Progenitor Cells Are Recruited to the Bone-Forming Site by the CXCR4/Stromal Cell-Derived Factor-1 Pathway

^aDivision of Gene Therapy Science and
^bDepartment of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan

Key Words. Bone marrow cells • Chemokine receptor CXCR4 • Mobilization kinetics • Osteoblast • Peripheral blood Stromal derived factor-1 • Stem/progenitor cell • Tissue regeneration

Correspondence: Katsuto Tamai, M.D., Ph.D., Division of Gene Therapy Science, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan. Telephone: 81-6-6879-3901; Fax: 81-6-6879-3909; e-mail: tamai{at}gts.med.osaka-u.ac.jp

Received July 1, 2007; accepted for publication September 28, 2007.
First published online in STEM CELLS EXPRESS   October 11, 2007.



Previous studies demonstrated the existence of osteoblastic cells in circulating blood. Recently, we reported that osteoblast progenitor cells (OPCs) in circulation originated from bone marrow and contributed to the formation of ectopic bone induced by implantation of a bone morphogenetic protein (BMP)-2-containing collagen pellet in mouse muscular tissue. However, the character of circulating bone marrow-derived osteoblast progenitor cells (MOPCs) and the precise mechanisms involving the circulating MOPCs in the osteogenic processes, such as signals that recruit the circulating MOPCs to the osseous tissues, have been obscure. In this report, we demonstrated for the first time that the MOPCs were mobilized from intact bones to transiently occupy approximately 80% of the mononuclear cell population in the circulating blood by BMP-2-pellet implantation. The mobilized MOPCs in the circulation did not express the hematopoietic marker CD45 on their surface, but they expressed CD44 and CXCR4, receptors of osteopontin and stromal cell-derived factor-1 (SDF-1), respectively. The MOPCs isolated from the mouse peripheral blood showed the ability to be osteoblasts in vitro and in vivo. Furthermore, the MOPCs in the circulation efficiently migrated to the region of bone formation by chemoattraction of SDF-1 expressed in vascular endothelial cells and the de novo osteoblasts of the region. These data may provide a novel insight into the mechanism of bone formation involving MOPCs in circulating blood, as well as perspective on the use of circulating MOPCs to accelerate bone regeneration in the future.

Disclosure of potential conflicts of interest is found at the end of this article.