The Regulation of Differentiation in Mesenchymal Stem Cells

被引:340
作者
Augello, Andrea [1 ]
De Bari, Cosimo [1 ]
机构
[1] Univ Aberdeen, Inst Med Sci, Bone & Musculoskeletal Res Programme, Regenerat Med Unit, Aberdeen AB25 2ZD, Scotland
关键词
BONE MORPHOGENETIC PROTEIN-2; MARROW STROMAL CELLS; SUPPRESSES OSTEOGENIC DIFFERENTIATION; VITRO CARTILAGE FORMATION; EPIDERMAL-GROWTH-FACTOR; EX-VIVO EXPANSION; IN-VITRO; CHONDROGENIC DIFFERENTIATION; N-CADHERIN; TGF-BETA;
D O I
10.1089/hum.2010.173
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Mesenchymal stromal/stem cells (MSCs) are a population of stromal cells present in the bone marrow and most connective tissues, capable of differentiation into mesenchymal tissues such as bone and cartilage. MSCs are attractive candidates for biological cell-based tissue repair approaches because of their extensive proliferative ability in culture while retaining their mesenchymal multilineage differentiation potential. In addition to its undoubted scientific interest, the prospect of monitoring and controlling MSC differentiation is a crucial regulatory and clinical requirement. Hence, the molecular regulation of MSC differentiation has been extensively studied. Most of the studies are in vitro, because the identity of MSCs in their tissues of origin in vivo remains undefined. This review addresses the current knowledge of the molecular basis of differentiation of cultured MSCs, with a particular focus on chondrogenesis and osteogenesis. Building on the information coming from developmental biology studies of embryonic skeletogenesis, several signaling pathways and transcription factors have been investigated and shown to play critical roles in MSC differentiation. In particular, the Wnt and transforming growth factor-beta/bone morphogenetic protein signaling pathways are well known to modulate in MSCs the molecular differentiation into cartilage and bone. Relevant to the emerging concept of stem cell niches is the demonstration that physical factors can also participate in the regulation of MSC differentiation. Knowledge of the regulation of MSC differentiation will be critical in the design of three-dimensional culture systems and bioreactors for automated bioprocessing through mathematical models applied to systems biology and network science.
引用
收藏
页码:1226 / 1238
页数:13
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