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ALK5-Mediated Transforming Growth Factor β Signaling in Neural Crest Cells Controls Craniofacial Muscle Development via Tissue-Tissue Interactions

机译:神经rest细胞中ALK5介导的转化生长因子β信号传导通过组织间相互作用控制颅面肌发育

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摘要

The development of the craniofacial muscles requires reciprocal interactions with surrounding craniofacial tissues that originate from cranial neural crest cells (CNCCs). However, the molecular mechanism involved in the tissue-tissue interactions between CNCCs and muscle progenitors during craniofacial muscle development is largely unknown. In the current study, we address how CNCCs regulate the development of the tongue and other craniofacial muscles using Wnt1-Cre; Alk5fl/fl mice, in which loss of Alk5 in CNCCs results in severely disrupted muscle formation. We found that Bmp4 is responsible for reduced proliferation of the myogenic progenitor cells in Wnt1-Cre; Alk5fl/fl mice during early myogenesis. In addition, Fgf4 and Fgf6 ligands were reduced in Wnt1-Cre; Alk5fl/fl mice and are critical for differentiation of the myogenic cells. Addition of Bmp4 or Fgf ligands rescues the proliferation and differentiation defects in the craniofacial muscles of Alk5 mutant mice in vitro. Taken together, our results indicate that CNCCs play critical roles in controlling craniofacial myogenic proliferation and differentiation through tissue-tissue interactions.
机译:颅面肌肉的发育需要与周围颅面组织的相互相互作用,而颅面组织起源于颅神经c细胞(CNCC)。但是,在颅面肌发育过程中,CNCC与肌肉祖细胞之间的组织相互作用中涉及的分子机制尚不清楚。在当前的研究中,我们探讨了使用Wnt1-Cre的CNCC如何调节舌头和其他颅面肌的发育。 Alk5 fl / fl 小鼠,其中CNCC中Alk5的丢失导致严重破坏了肌肉的形成。我们发现,Bmp4负责减少Wnt1-Cre中成肌祖细胞的增殖。 Alk5 fl / fl 小鼠在早期成肌过程中。此外,Wnt1-Cre中的Fgf4和Fgf6配体减少了。 Alk5 fl / fl 小鼠对于成肌细胞的分化至关重要。 Bmp4或Fgf配体的添加可以在体外挽救Alk5突变小鼠颅面肌的增殖和分化缺陷。综上所述,我们的结果表明CNCC在通过组织与组织的相互作用控制颅面肌成肌增殖和分化中起着关键作用。

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