Drosophila morphogenesis: tissue force laws and the modeling of dorsal closure

被引:27
作者
Layton, Anita T. [2 ]
Toyama, Yusuke [1 ]
Yang, Guo-Qiang [2 ]
Edwards, Glenn S. [1 ]
Kiehart, Daniel P. [3 ]
Venakides, Stephanos [2 ]
机构
[1] Duke Univ, Dept Phys, Durham, NC 27708 USA
[2] Duke Univ, Dept Math, Durham, NC 27708 USA
[3] Duke Univ, Dept Biol, Durham, NC 27708 USA
来源
HFSP JOURNAL | 2009年 / 3卷 / 06期
关键词
EPITHELIAL MORPHOGENESIS; CELL-ADHESION; MOVEMENT; INTEGRIN; MICROSURGERY; MECHANISM; EMBRYO;
D O I
10.2976/1.3266062
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dorsal closure, a stage of Drosophila development, is a model system for cell sheet morphogenesis and wound healing. During closure, two flanks of epidermal tissue progressively advance to reduce the area of the eye-shaped opening in the dorsal surface, which contains amnioserosa tissue. To simulate the time evolution of the overall shape of the dorsal opening, we developed a mathematical model, in which contractility and elasticity are manifest in model force-producing elements that satisfy force-velocity relationships similar to muscle. The action of the elements is consistent with the force-producing behavior of actin and myosin in cells. The parameters that characterize the simulated embryos were optimized by reference to experimental observations on wild-type embryos and, to a lesser extent, on embryos whose amnioserosa was removed by laser surgery and on myospheroid mutant embryos. Simulations failed to reproduce the amnioserosa-removal protocol in either the elastic or the contractile limit, indicating that both elastic and contractile dynamics are essential components of the biological force-producing elements. We found it was necessary to actively upregulate forces to recapitulate both the double and single-canthus nick protocols, which did not participate in the optimization of parameters, suggesting the existence of additional key feedback mechanisms. [DOI: 10.2976/1.3266062]
引用
收藏
页码:441 / 460
页数:20
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