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First published online January 10, 2008
Stem Cells Vol. 26 No. 3 March 2008, pp. 682 -691
doi:10.1634/stemcells.2007-0738; www.StemCells.com
© 2008 AlphaMed Press

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TISSUE-SPECIFIC STEM CELLS

Functional Structure of Adipocytes Differentiated from Human Umbilical Cord Stroma-Derived Stem Cells

Sercin Karahuseyinoglua, Cetin Kocaefeb, Deniz Balcia, Esra Erdemlia, Alp Cana

aDepartment of Histology and Embryology, Ankara University School of Medicine, Ankara, Turkey;
bDepartment of Medical Biology, Hacettepe University School of Medicine, Ankara, Turkey

Key Words. Adipocyte • Differentiation • Human • Lipid • Mesenchymal stem cells • Umbilical cord

Correspondence: Alp Can, M.D., Department of Histology and Embryology, Ankara University School of Medicine, Sihhiye, 06100 Ankara, Turkey. Telephone: 90-312-3103010, ext. 369; Fax: 90-312-3106370; e-mail: alpcan{at}medicine.ankara.edu.tr

Received September 6, 2007; accepted for publication December 21, 2007.
First published online in STEM CELLS EXPRESS   January 10, 2008.



It has been previously demonstrated that human umbilical cord stroma-derived stem cells (HUCSCs) are competent to differentiate into adipocytes. However, controversies have arisen as to whether HUCSCs can become mature adipocytes or not, and to what extent these cells can be induced in adipogenic pathway. Here, we extensively analyzed their adipogenic potency with a structural and functional approach by determining lipid formation dynamics in concordance to adipocyte-specific markers. During a 35-day period, HUCSCs respond to adipogenic induction, at which point 88% of cells exhibited multilocular lipid granules (LGs) having a mean diameter of 3 µm in round-shaped, F-actin-poor cells. Although the 1st week of induction did not generally display typical lipidogenic phenotypes, the degree of adipogenesis was dissected and confirmed by mRNA expressions of peroxisome proliferator-activated receptor {gamma}, C/EBP-β, sterol regulatory element-binding transcription factor 1, adipophilin, stearoyl-CoA desaturase, glycerol 3-phosphate dehydrogenase 1, LIPE, adiponectin, and leptin. All markers tested were found elevated in various amounts (3–70-fold) around day 7 and reached a plateau after day 14 or 21 (5–335-fold). Perilipin as a surface protein around the LGs was confined exclusively to the enlarging LGs. Conclusively, we propose that after the termination of proliferation, HUCSCs possess the biochemical and cellular machinery to successfully differentiate into maturing adipocytes under adipogenic conditions, and this feature will ultimately allow these fetus-derived stem cells to be used for various therapeutic or esthetic purposes.

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







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