Molecular mechanisms of mechanical stress response during chondrogenesis

被引:0
|
作者
Takahashi, Ichiro [1 ]
Masuda, Taisuke [2 ]
Kohsaka, Kumiko [1 ]
Terao, Fumie [1 ]
Anada, Takahisa [2 ]
Sasano, Yasuyuki [3 ]
Takano-Yamamoto, Teruko [1 ]
Suzuki, Osamu [2 ]
机构
[1] Division of Orthodontics and Dentofacial Orthopedics, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, Japan
[2] Division of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Japan
[3] Division of Craniofacial Development and Regeneration, Tohoku University Graduate School of Dentistry, Japan
来源
关键词
Collagen - Enzyme activity - Bone - Cell signaling - Compressive stress - Shear stress - Stem cells - Histology - Gene expression - Joints (anatomy) - Cell culture - Shear flow;
D O I
10.1299/jbse.4.307
中图分类号
学科分类号
摘要
Muscloskeletal tissues, bone, cartilage, muscles and tendons regulate and support the body's actions and are differentiated from mesenchymal stem cells. These organs generate and/or respond to mechanical stress, which is inevitable in daily life. Among these tissues, cartilages play roles in articular function in joints where shear stress is loaded in combination with cyclical or intermittent compressive force by joint action, and provides a template for bone growth under compressive stress directed along the long axis of long bones. Along with soluble factors, such as cytokines and growth factors, mechanical stress has been recognized as one of the epigenetic factors that regulates the gene expression of various types of cells. Thus, the molecular mechanisms of the mechano-sensing, mechano-transduction, and mechano-response of cells have become a focus of connective tissue biology. Here, we will discuss the mechanisms through which differentiated chondrocytes and mesenchymal cells that are differentiating into chondrocytes respond to various types of mechanical stress by altering their phenotype and how these phenotypic changes are molecularly regulated. We will focus on the roles of cell-extracellular matrix interactions through integrins and downstream signaling pathways involving mitogen-activated protein kinases.
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页码:307 / 317
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