TWIST Family of Basic Helix-Loop-Helix Transcription Factors Mediate Human Mesenchymal Stem Cell Growth and Commitment
Autor: | Carlotta A. Glackin, Agnieszka Arthur, Stan Gronthos, Sandra Isenmann, Jenna L Turner, Songtao Shi, Andrew C.W. Zannettino |
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Rok vydání: | 2009 |
Předmět: |
Adult
Bone sialoprotein Stromal cell Down-Regulation Young Adult Osteogenesis Humans Cell Lineage Osteopontin Transcription factor Cells Cultured Cell Proliferation Adipogenesis Bone Development Osteoblasts biology Twist-Related Protein 1 Mesenchymal stem cell Nuclear Proteins Proteins Cell Differentiation Mesenchymal Stem Cells Cell Biology Cell biology Repressor Proteins RUNX2 Immunology biology.protein Molecular Medicine Stem cell Biomarkers Transcription Factors Developmental Biology |
Zdroj: | Stem Cells. 27:2457-2468 |
ISSN: | 1549-4918 1066-5099 |
DOI: | 10.1002/stem.181 |
Popis: | The TWIST family of basic helix-loop-helix transcription factors, Twist-1 and Dermo-1 are known mediators of mesodermal tissue development and contribute to correct patterning of the skeleton. In this study, we demonstrate that freshly purified human bone marrow-derived mesenchymal stromal/stem cells (MSC) express high levels of Twist-1 and Dermo-1 which are downregulated following ex vivo expansion. Enforced expression of Twist-1 or Dermo-1 in human MSC cultures increased expression of the MSC marker, STRO-1, and the early osteogenic transcription factors, Runx2 and Msx2. Conversely, overexpression of Twist-1 and Dermo-1 was associated with a decrease in the gene expression of osteoblast-associated markers, bone morphogenic protein-2, bone sialoprotein, osteopontin, alkaline phosphatase and osteocalcin. High expressing Twist-1 or Dermo-1 MSC lines exhibited an enhanced proliferative potential of approximately 2.5-fold compared with control MSC populations that were associated with elevated levels of Id-1 and Id-2 gene expression. Functional studies demonstrated that high expressing Twist-1 and Dermo-1 MSC displayed a decreased capacity for osteo/chondrogenic differentiation and an enhanced capacity to undergo adipogenesis. These findings implicate the TWIST gene family members as potential mediators of MSC self-renewal and lineage commitment in postnatal skeletal tissues by exerting their effects on genes involved in the early stages of bone development. |
Databáze: | OpenAIRE |
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