Thursday, March 4, 2010

3/5 pubmed: adipose stem cell

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Comparative Review of Growth Factors for Induction of 3-Dimensional in vitro Chondrogenesis in Human Mesenchymal Stem Cells Isolated from Bone Marrow and Adipose Tissue.
March 4, 2010 at 11:39 AM

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Comparative Review of Growth Factors for Induction of 3-Dimensional in vitro Chondrogenesis in Human Mesenchymal Stem Cells Isolated from Bone Marrow and Adipose Tissue.

Tissue Eng Part B Rev. 2010 Mar 2;

Authors: Puetzer JL, Petitte J, Loboa E

The ability of bone marrow derived mesenchymal stem cells (MSCs) and adipose derived stem cells (ASCs) to undergo chondrogenic differentiation has been studied extensively and it has been suggested that the chondrogenic potential of these stem cells differ from each other. Here, we provide a comprehensive review and analysis of the various growth factor induction agents for MSC and ASC 3D in vitro chondrogenic differentiation. In general, the most common growth factors for chondrogenic induction come from the transforming growth factor beta (TGF-beta) superfamily. To date, the most promising growth factors for chondrogenesis appear to be TGFbeta-3 and bone morphogenetic protein (BMP)-6. A thorough review of the literature indicates that human MSCs (hMSCs) appear to exhibit the highest chondrogenic potential in 3D culture in medium containing both dexamethasone and TGFbeta-3. Some reports indicate that the addition of BMP-6 to TFGbeta-3 and dexamethasone further in! creases hMSC chondrogenesis; but these results are still not consistently supported. Induction of human ASC (hASC) chondrogenesis appears most successful when dexamethasone, TGFbeta-3, and BMP-6 are used in combination. However, to date current formulations do not always result in stable differentiation to the chondrocytic lineage by hMSCs and hASCs. Continued research must be performed to examine the expression cascades of the TFG-beta superfamily to further determine the effects of each growth factor alone, and in combination, on these stem cell lines.

PMID: 20196646 [PubMed - as supplied by publisher]

 

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