Extracellular matrix remodeling accompanies axial muscle development and morphogenesis in the mouse

被引:22
|
作者
Deries, Marianne [1 ]
Goncalves, Andre B. [1 ]
Vaz, Raquel [1 ]
Martins, Gabriel G. [1 ,2 ]
Rodrigues, Gabriela [1 ,2 ]
Thorsteinsdottir, Solveig [1 ,2 ]
机构
[1] Univ Lisbon, Fac Ciencias, Dept Biol Anim, Ctr Biol Ambiental, Lisbon, Portugal
[2] Inst Gulbenkian Ciencias, Oeiras, Portugal
关键词
mouse embryo; skeletal muscle development; dermomyotome; myotome; extracellular matrix; fibronectin; tenascin; laminin; integrins; 3D analysis; SKELETAL-MUSCLE; MYOTOME FORMATION; PROGENITOR CELLS; AVIAN EMBRYO; TENASCIN-C; FIBRONECTIN MATRIX; MAMMALIAN MYOTOME; INTEGRIN SUBUNIT; MYOGENIC CELLS; EXPRESSION;
D O I
10.1002/dvdy.23703
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Background: Skeletal myogenesis is extensively influenced by the surrounding environment. However, how the extracellular matrix (ECM) affects morphogenesis of muscles is not well understood. Results: We mapped the three-dimensional (3D) organization of fibronectin, tenascin, and laminin by immunofluorescence during early epaxial myogenesis in mouse embryos. We define four stages of dermomyotome/myotome development and reveal the 3D organization of myogenic cells within their ECM during those stages. Fibronectin is abundant in all interstitial tissues, while tenascin is restricted to intersegmental borders. Bundles of fibronectin and tenascin also penetrate into the myotome, possibly promoting myocyte alignment. A laminin matrix delineates the dermomyotome and myotome and undergoes dynamic changes, correlating with key developmental events. Conclusion: Our observations cast new light on how myotomal cells interact with their environment and suggest that, as the segmented myotomes transform into the epaxial muscle masses, the laminin matrix disassembles and myocytes use the abundant fibronectin matrix to reach their final organization. Developmental Dynamics 241:350364, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:350 / 364
页数:15
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