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Mesenchymal precursor cells in the blood of normal individuals

Nathan J Zvaifler1 email, Lilla Marinova-Mutafchieva2, Gill Adams2, Christopher J Edwards2, Jill Moss3, Jan A Burger1 and Ravinder N Maini2,3

1Department of Medicine, University of California, San Diego, CA, USA

2Kennedy Institute of Rheumatology, London, UK

3Department of Pathology and Medicine, Imperial College School of Medicine, Charing Cross Hospital, London, UK

author email

Arthritis Res 2000, 2:477-488doi:10.1186/ar130

Published: 31 August 2000

Abstract

Mesenchymal precursor cells found in the blood (BMPCs) of normal persons adhere to plastic and glass and proliferate logarithmically in DMEM-20% fetal calf serum (FCS) without growth factors. They form cells with fibroblast-like and stromal morphology, which is not affected by eliminating CD34, CD3, or CD14 cells. Osteogenic supplements (dexamethasone, ascorbic acid, and β-glycerophosphate) added to the culture inhibited fibroblast formation, and BMPCs assumed the cuboidal shape of osteoblasts. After 5 days in supplemented medium, the elutriated cells displayed alkaline phosphatase (AP), and the addition of bone morphogenetic protein (BMP)2 (1 ng) doubled AP production (P < 0.04). Two weeks later, 30% of the cells were very large and reacted with anti-osteocalcin antibody. The same cultures also contained sudanophlic adipocytes and multinucleated giant cells that stained for tartrate-resistant acid phosphatase (TRAP) and vitronectin receptors. Cultured BMPCs immunostain with antibodies to vimentin, type I collagen, and BMP receptors, heterodimeric structures expressed on mesenchymal lineage cells. In addition, BMPCs stain with anti-CD105 (endoglin), a putative marker for bone-marrow mesenchymal stem cells (MSCs).


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