Physical forces drive C. elegans embryonic deformation

被引:0
|
作者
Wang, Ting [1 ,2 ]
Ben Amar, Martine [1 ]
机构
[1] Univ Paris Cite, Sorbonne Univ, Univ PSL, Lab Phys,Ecole Normale Super,CNRS, F-75005 Paris, France
[2] Tongji Univ, Sch Aerosp Engn & Appl Mech, 1239 Siping Rd, Shanghai 200092, Peoples R China
关键词
C; elegans; Active stress; Muscle contractions; Elongation; Torsion deformation; MORPHOGENESIS; MODEL; GROWTH; CYTOSKELETON; ELONGATION; STRESS; SHEAR;
D O I
10.1016/j.ijnonlinmec.2024.104833
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
The abnormal development of embryos is closely linked to abnormal cell division and elongation, but the underlying mechanism remains to be elucidated. The embryonic development of C elegans embryo is different because it occurs without cell proliferation or cell rearrangement. Here, we focus on a spectacular 4-fold elongation that is achieved approximately 3 h before the egg shell hatches and results from active filament networks. The body shape is represented by an inhomogeneous cylinder, which allows us to assess the active stresses induced by the actomyosin network located in the cortex and the muscles in ventral position near the epidermis. By considering the specific embryo configuration, we can quantitatively obtain the contractile forces induced by actomyosin filaments and muscles for a bending torsion event with defined curvature. We find that the active stress induced by actomyosin molecular motors or muscles increases with elongation and bending curvature, while also varying with radius. Both elongation and torsional deformation contribute to increased moment magnitudes that explain the dynamics of the embryo in the egg. Our results highlight the complex interplay between biomechanical factors in modulating embryonic deformation.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Forces drive basement membrane invasion in Caenorhabditis elegans
    Caceres, Rodrigo
    Bojanala, Nagagireesh
    Kelley, Laura C.
    Dreier, Jes
    Manzi, John
    Di Federico, Fahima
    Chi, Qiuyi
    Risler, Thomas
    Testa, Ilaria
    Sherwood, David R.
    Plastino, Julie
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (45) : 11537 - 11542
  • [22] The mevalonate pathway in C. Elegans
    Rauthan, Manish
    Pilon, Marc
    LIPIDS IN HEALTH AND DISEASE, 2011, 10
  • [23] Neuronal Polarity in C. elegans
    Ou, Chan-Yen
    Shen, Kang
    DEVELOPMENTAL NEUROBIOLOGY, 2011, 71 (06) : 554 - 566
  • [24] C. elegans Chemotaxis Assay
    Margie, Olivia
    Palmer, Chris
    Chin-Sang, Ian
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2013, (74):
  • [25] Autophagy in C. elegans development
    Palmisano, Nicholas J.
    Melendez, Alicia
    DEVELOPMENTAL BIOLOGY, 2019, 447 (01) : 103 - 125
  • [26] Unraveling effects of anti-aging drugs on C. elegans using liposomes
    Zhang, Aihan
    Hsiung, Kuei Ching
    Kern, Carina C.
    Wang, Yuting
    Girtle, Anna L.
    Xu, Nuo
    Gems, David
    GEROSCIENCE, 2023, 45 (03) : 1583 - 1603
  • [27] Sequential Rosettes Drive C. elegans Ventral Nerve Cord Assembly
    Soto, Martha C.
    DEVELOPMENTAL CELL, 2017, 41 (02) : 121 - 122
  • [28] Crosslinking activity of non-muscle myosin II is not sufficient for embryonic cytokinesis in C. elegans
    Osorio, Daniel S.
    Chan, Fung-Yi
    Saramago, Joana
    Leite, Joana
    Silva, Ana M.
    Sobral, Ana F.
    Gassmann, Reto
    Carvalho, Ana Xavier
    DEVELOPMENT, 2019, 146 (21):
  • [29] A possible role for FRM-1, a C. elegans FERM family protein, in embryonic development
    Choi, Boram
    Kang, Junsu
    Park, Yang-Seo
    Lee, Junho
    Cho, Nam Jeong
    MOLECULES AND CELLS, 2011, 31 (05) : 455 - 459
  • [30] Semaphorin signaling restricts neuronal regeneration in C. elegans
    Harreguy, Maria B.
    Tanvir, Zainab
    Shah, Esha
    Simprevil, Blandine
    Tran, Tracy S.
    Haspel, Gal
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 10