## Abstract Availability of human chondrocytes is a major limiting factor regarding drug discovery projects and tissue replacement therapies. As an alternative human mesenchymal stem cells (hMSCs) from bone marrow are taken into consideration as they can differentiate along the chondrogenic lineage
Differentiation of human mesenchymal stem cells and articular chondrocytes: Analysis of chondrogenic potential and expression pattern of differentiation-related transcription factors
โ Scribed by Camilla Karlsson; Camilla Brantsing; Teresia Svensson; Helena Brisby; Julia Asp; Tommi Tallheden; Anders Lindahl
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 435 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0736-0266
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Mesenchymal stem cells (MSCs) are a candidate for replacing chondrocytes in cellโbased repair of cartilage lesions. However, it has not been clarified if these cells can acquire the hyaline phenotype, and whether chondrocytes and MSCs show the same expression patterns of critical control genes in development. In order to study this, articular chondrocytes and iliac crest derived MSCs were allowed to differentiate in pellet mass cultures. Gene expression of markers for the cartilage phenotype, helixโloopโhelix (HLH) transcription factors, and chondrogenic transcription factors were analyzed by realโtime PCR. Matrix production was assayed using biochemical analysis for hydroxyproline, glycosaminoglycans, and immunohistochemistry for collagen types I and II. Significantly decreased expression of collagen type I was accompanied by increased expression of collagen types IIA and IIB during differentiation of chondrocytes, indicating differentiation towards a hyaline phenotype. Chondrogenesis in MSCs on the other hand resulted in upโregulation of collagen types I, IIA, IIB, and X, demonstrating differentiation towards cartilage of a mixed phenotype. Expression of HES1 increased significantly during chondrogenesis in chondrocytes while expression in MSCs was maintained at a low level. The HLH gene HES5 on the other hand was only detected in chondrocytes. Expression of ID1 decreased significantly in chondrocytes while the opposite was seen in MSCs. These findings suggest that chondrocytes and MSCs differentiated and formed different subtypes of cartilage, the hyaline and a mixed cartilage phenotype, respectively. Differentially regulated HLH genes indicated the possibility for HLH proteins in regulating chondrogenic differentiation. This information is important to understand the potential use of MSCs in cartilage repair. ยฉ 2006 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 25:152โ163, 2007
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