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Characterizing the role of Pdgfra in calvarial development

  • Meenakshi Umar
  • , Garrett Bartoletti
  • , Chunmin Dong
  • , Apurva Gahankari
  • , Danielle Browne
  • , Alastair Deng
  • , Josue Jaramillo
  • , Mimi Sammarco
  • , Jennifer Simkin
  • , Fenglei He

Producción científica: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

Background: Mammalian calvarium is composed of flat bones developed from two origins, neural crest, and mesoderm. Cells from both origins exhibit similar behavior but express distinct transcriptomes. It is intriguing to ask whether genes shared by both origins play similar or distinct roles in development. In the present study, we have examined the role of Pdgfra, which is expressed in both neural crest and mesoderm, in specific lineages during calvarial development. Results: We found that in calvarial progenitor cells, Pdgfra is needed to maintain normal proliferation and migration of neural crest cells but only proliferation of mesoderm cells. Later in calvarial osteoblasts, we found that Pdgfra is necessary for both proliferation and differentiation of neural crest-derived cells, but not for differentiation of mesoderm-derived cells. We also examined the potential interaction between Pdgfra and other signaling pathway involved in calvarial osteoblasts but did not identify significant alteration of Wnt or Hh signaling activity in Pdgfra genetic models. Conclusions: Pdgfra is required for normal calvarial development in both neural crest cells and mesoderm cells, but these lineages exhibit distinct responses to alteration of Pdgfra activity.

Idioma originalEnglish
Páginas (desde-hasta)589-604
Número de páginas16
PublicaciónDevelopmental Dynamics
Volumen252
N.º5
DOI
EstadoPublished - may 2023

Nota bibliográfica

Publisher Copyright:
© 2023 American Association for Anatomy.

Financiación

The authors thank Emily Orsino and Gerrit Holleman for their excellent genotyping work. The authors are grateful to our lab colleagues for their critical and constructive comments. This work was supported by Tulane University and NIH/National Institute of Dental and Craniofacial Research Grant DE028918 to F.H.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute of Dental and Craniofacial ResearchDE028918
Tulane University

    ASJC Scopus subject areas

    • Developmental Biology

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