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Stem Cells Vol. 25 No. 1 January 2007, pp. 125 -131
doi:10.1634/stemcells.2006-0295; www.StemCells.com
© 2007 AlphaMed Press

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TISSUE-SPECIFIC STEM CELLS

Multilineage Differentiation and Characterization of the Human Fetal Osteoblastic 1.19 Cell Line: A Possible In Vitro Model of Human Mesenchymal Progenitors

Men-luh Yena,b, Chih-Cheng Chienc,d, Ing-ming Chiue,f, Hsing-I Huangc,g, Yao-Chang Chenh, Hsin-I Hua,b, B. Linju Yend,e

Departments of aPrimary Care Medicine and
bObstetrics/Gynecology, National Taiwan University Hospital and College of Medicine, National Taiwan University, Taipei, Taiwan;
cDepartment of Medicine, School of Medicine, Fu Jen Catholic University, Taipei, Taiwan;
dCathay General Hospital, Neihu, Taiwan;
eStem Cell Research Center, National Health Research Institutes, Zhunan, Taiwan;
fInstitute of Medical Technology, National Chung Hsing University, Taichung;
gCathay Medical Research Institute, Cathay General Hospital, Taipei, Taiwan;
hDepartment of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan

Key Words. Mesenchymal stem cells • Multilineage differentiation • Nestin • Oct-4 • Osteoprogenitor • Cell line

Correspondence: B. Linju Yen, M.D., Stem Cell Research Center, National Health Research Institutes, 35 Keyan Road, Zhunan, 350, Taiwan. Telephone: 886-2-2653-4401, ext. 27502; Fax: 886-2-2792-9679; e-mail: blyen{at}nhri.org.tw

Received May 19, 2006; accepted for publication September 14, 2006.


The in vitro study of human bone marrow mesenchymal stromal cells (BMMSCs) has largely depended on the use of primary cultures. Although these are excellent model systems, their scarcity, heterogeneity, and limited lifespan restrict their usefulness. This has led researchers to look for other sources of MSCs, and recently, such a population of progenitor/stem cells has been found in mesodermal tissues, including bone. We therefore hypothesized that a well-studied and commercially available clonal human osteoprogenitor cell line, the fetal osteoblastic 1.19 cell line (hFOB), may have multilineage differentiation potential. We found that undifferentiated hFOB cells possess similar cell surface markers as BMMSCs and also express the embryonic stem cell-related pluripotency gene, Oct-4, as well as the neural progenitor marker nestin. hFOB cells can also undergo multilineage differentiation into the mesodermal lineages of chondrogenic and adipocytic cell types in addition to its predetermined pathway, the mature osteoblast. Moreover, as with BMMSCs, under neural-inducing conditions, hFOB cells acquire a neural-like phenotype. This human cell line has been a widely used model of normal osteoblast differentiation. Our data suggest that hFOB cells may provide for researchers an easily available, homogeneous, and consistent in vitro model for study of human mesenchymal progenitor cells.







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