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a First Department of Pathology,
b Regeneration Research Center for Intractable Diseases,
c Department of Transplantation for Regeneration Therapy, Kansai Medical University, Moriguchi City, Osaka, Japan;
d Department of Biotechnology, Kyoto Institute of Technology, Kyoto, Japan;
e Department of Toxicology, School of Public Health, Jilin University, Changchun, China;
f Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis, Davis, California, USA
Key Words. Mesenchymal stem cells • Hematopoietic stem cells • Bone marrow cells • PA6 • Mouse
Correspondence: Susumu Ikehara, M.D., Ph.D., First Department of Pathology, Kansai Medical University, 10-15 Fumizono-cho, Moriguchi City, Osaka 570-8506, Japan. Telephone: +81-6-6993-9429; Fax: +81-6-6994-8283; e-mail: ikehara{at}takii.kmu.ac.jp.
Received May 16, 2005;
accepted for publication August 30, 2005.
Mesenchymal stem cells (MSCs) are defined as cells that can differentiate into multiple mesenchymal lineage cells. MSCs have some features (surface molecules and cytokine production, etc.) common to so-called traditional bone marrow (BM) stromal cells, which have the capacity to support hemopoiesis. In the present study, we isolated murine MSCs (mMSCs) from the fetal BM using an anti-PA6 monoclonal antibody (mAb) that is specific for bone marrow stromal cells. The mMSCs, called FMS/PA6-P cells, are adherent, fibroblastic, and extensively expanded and have the ability to differentiate not only into osteoblasts and adipocytes but also into vascular endothelial cells. The FMS/PA6-P cells produce a broad spectrum of cytokines and growth factors closely related to hemopoiesis and show good hemopoiesis-supporting capacity both in vivo and in vitro, suggesting that they are a component of the hemopoietic stem cell niche in vivo. Interestingly, although the FMS/PA6-P cells express a high level of the PA6 molecule, which is reactive with anti-PA6 mAb, they gradually lose their ability to express this molecule during the course of differentiation into osteoblasts and adipocytes, indicating that the PA6 molecule might serve as a novel marker of mMSCs.
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