G-Protein α-Subunit Gsα Is Required for Craniofacial Morphogenesis

PLoS One. 2016 Feb 9;11(2):e0147535. doi: 10.1371/journal.pone.0147535. eCollection 2016.

Abstract

The heterotrimeric G protein subunit Gsα couples receptors to activate adenylyl cyclase and is required for the intracellular cAMP response and protein kinase A (PKA) activation. Gsα is ubiquitously expressed in many cell types; however, the role of Gsα in neural crest cells (NCCs) remains unclear. Here we report that NCCs-specific Gsα knockout mice die within hours after birth and exhibit dramatic craniofacial malformations, including hypoplastic maxilla and mandible, cleft palate and craniofacial skeleton defects. Histological and anatomical analysis reveal that the cleft palate in Gsα knockout mice is a secondary defect resulting from craniofacial skeleton deficiencies. In Gsα knockout mice, the morphologies of NCCs-derived cranial nerves are normal, but the development of dorsal root and sympathetic ganglia are impaired. Furthermore, loss of Gsα in NCCs does not affect cranial NCCs migration or cell proliferation, but significantly accelerate osteochondrogenic differentiation. Taken together, our study suggests that Gsα is required for neural crest cells-derived craniofacial development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cleft Palate / embryology
  • Cleft Palate / genetics
  • Facial Bones / abnormalities
  • Facial Bones / embryology*
  • GTP-Binding Protein alpha Subunits, Gs / deficiency
  • GTP-Binding Protein alpha Subunits, Gs / genetics
  • GTP-Binding Protein alpha Subunits, Gs / metabolism*
  • Ganglia, Sympathetic / embryology
  • Gene Knockout Techniques
  • Mice
  • Morphogenesis*
  • Mutation
  • Neural Crest / cytology
  • Neural Crest / metabolism
  • Skull / abnormalities
  • Skull / embryology*
  • Spinal Nerve Roots / embryology

Substances

  • GTP-Binding Protein alpha Subunits, Gs

Grants and funding

This work was partially supported by grants from the Ministry of Science & Technology-China (2014CB964600, 2012CB966800,2013ZX09509104, 2007CB947202,2009CB941402, 2010CB945600, 2011CB965100, 2013ZX09509104, and 2009R0002), National Science Foundation of China (31301125, 30771102, 31071283,81370457, 81271498), Shenzhen Peacock Plan (No. KQCX20130628112914292), and faculty development support (West China Women's & Children Hospital & Shenzhen Institutes of Advanced Technology-CAS &Tongji University Shanghai East Hospital) and Shenzhen Key Laboratory for Molecular Biology of Neural Development (ZDSY20120617112838879). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.