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Tbx4 和 tbx5 在结缔组织中的作用对于肢体肌肉和肌腱的模式形成是必需的。

Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning.

机构信息

Division of Developmental Biology, MRC-National Institute for Medical Research, Mill Hill, London NW7 1AA, United Kingdom.

出版信息

Dev Cell. 2010 Jan 19;18(1):148-56. doi: 10.1016/j.devcel.2009.11.013.

Abstract

Proper functioning of the musculoskeletal system requires the precise integration of bones, muscles, and tendons. Complex morphogenetic events ensure that these elements are linked together in the appropriate three-dimensional configuration. It has been difficult, however, to tease apart the mechanisms that regulate tissue morphogenesis. We find that deletion of Tbx5 in forelimbs (or Tbx4 in hindlimbs) specifically affects muscle and tendon patterning without disrupting skeletal development, thus suggesting that distinct cues regulate these processes. We identify muscle connective tissue as the site of action of these transcription factors and show that N-Cadherin and beta-Catenin are key downstream effectors acting in muscle connective tissue and regulating soft-tissue morphogenesis. In humans, TBX5 mutations lead to Holt-Oram syndrome, which is characterized by forelimb musculoskeletal defects. Our results suggest that a focus on connective tissue is required to understand the etiology of diseases affecting soft tissue formation.

摘要

骨骼肌肉系统的正常运作需要骨骼、肌肉和肌腱的精确整合。复杂的形态发生事件确保这些元素以适当的三维结构连接在一起。然而,要理清调节组织形态发生的机制一直很困难。我们发现,Tbx5 在前肢(或 Tbx4 在后肢)中的缺失特异性地影响肌肉和肌腱模式形成,而不会破坏骨骼发育,这表明不同的线索调节这些过程。我们确定肌肉结缔组织是这些转录因子作用的部位,并表明 N-钙黏蛋白和β-连环蛋白是在肌肉结缔组织中起作用并调节软组织形态发生的关键下游效应物。在人类中,TBX5 突变导致 Holt-Oram 综合征,其特征是前肢骨骼肌肉缺陷。我们的结果表明,需要关注结缔组织,以了解影响软组织形成的疾病的病因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65d1/3034643/7016e8ab3c9d/nihms-164560-f0001.jpg

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