Mechanical control of tissue morphogenesis

被引:106
作者
Patwari, Parth
Lee, Richard T.
机构
[1] Brigham & Womens Hosp, Div Cardiovasc, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
关键词
mechanotransduction; cytoskeleton; shear stress; embryonic development; stem cells;
D O I
10.1161/CIRCRESAHA.108.175331
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mechanical forces participate in morphogenesis from the level of individual cells to whole organism patterning. This article reviews recent research that has identified specific roles for mechanical forces in important developmental events. One well defined example is that dynein-driven cilia create fluid flow that determines left-right patterning in the early mammalian embryo. Fluid flow is also important for vasculogenesis, and evidence suggests that fluid shear stress rather than fluid transport is primarily required for remodeling the early vasculature. Contraction of the actin cytoskeleton, driven by nonmuscle myosins and regulated by the Rho family GTPases, is a recurring mechanism for controlling morphogenesis throughout development, from gastrulation to cardiogenesis. Finally, novel experimental approaches suggest critical roles for the actin cytoskeleton and the mechanical environment in determining differentiation of mesenchymal stem cells. Insights into the mechanisms linking mechanical forces to cell and tissue differentiation pathways are important for understanding many congenital diseases and for developing regenerative medicine strategies.
引用
收藏
页码:234 / 243
页数:10
相关论文
共 101 条
  • [1] STAGE-RELATED CAPACITY FOR LIMB CHONDROGENESIS IN CELL-CULTURE
    AHRENS, PB
    SOLURSH, M
    REITER, RS
    [J]. DEVELOPMENTAL BIOLOGY, 1977, 60 (01) : 69 - 82
  • [2] Heart valve development - Endothelial cell signaling and differentiation
    Armstrong, EJ
    Bischoff, J
    [J]. CIRCULATION RESEARCH, 2004, 95 (05) : 459 - 470
  • [3] The compliance of collagen gels regulates transforming growth factor-β induction of α-smooth muscle actin in fibroblasts
    Arora, PD
    Narani, N
    McCulloch, CAG
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (03) : 871 - 882
  • [4] ASHBY M, 1995, STEVENAGE
  • [5] DRhoGEF2 regulates actin organization and contractility in the Drosophila blastoderm embryo
    Barmchi, MP
    Rogers, S
    Häcker, U
    [J]. JOURNAL OF CELL BIOLOGY, 2005, 168 (04) : 575 - 585
  • [6] Mechanics and function in heart morphogenesis
    Bartman, T
    Hove, J
    [J]. DEVELOPMENTAL DYNAMICS, 2005, 233 (02) : 373 - 381
  • [7] Early myocardial function affects endocardial cushion development in zebrafish
    Bartman, T
    Walsh, EC
    Wen, KK
    McKane, M
    Ren, JH
    Alexander, J
    Rubenstein, PA
    Stainier, DYR
    [J]. PLOS BIOLOGY, 2004, 2 (05) : 673 - 681
  • [8] MICROFILAMENT MODIFICATION BY DIHYDROCYTOCHALASIN-B CAUSES RETINOIC ACID-MODULATED CHONDROCYTES TO REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WITHOUT A CHANGE IN SHAPE
    BENYA, PD
    BROWN, PD
    PADILLA, SR
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 106 (01) : 161 - 170
  • [9] DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS
    BENYA, PD
    SHAFFER, JD
    [J]. CELL, 1982, 30 (01) : 215 - 224
  • [10] Interstitial flow as a guide for lymphangiogenesis
    Boardman, KC
    Swartz, MA
    [J]. CIRCULATION RESEARCH, 2003, 92 (07) : 801 - 808