Early thyroid development requires a Tbx1-Fgf8 pathway

Gabriella Lania, Zhen Zhang, Tuong Huynh, Cinzia Caprio, Anne M. Moon, Francesca Vitelli, Antonio Baldini

Research output: Contribution to journalArticlepeer-review

Abstract

The thyroid develops within the pharyngeal apparatus from endodermally-derived cells. The many derivatives of the pharyngeal apparatus develop at similar times and sometimes from common cell types, explaining why many syndromic disorders express multiple birth defects affecting different structures that share a common pharyngeal origin. Thus, different derivatives may share common genetic networks during their development. Tbx1, the major gene associated with DiGeorge syndrome, is a key player in the global development of the pharyngeal apparatus, being required for virtually all its derivatives, including the thyroid. Here we show that Tbx1 regulates the size of the early thyroid primordium through its expression in the adjacent mesoderm. Because Tbx1 regulates the expression of Fgf8 in the mesoderm, we postulated that Fgf8 mediates critical Tbx1-dependent interactions between mesodermal cells and endodermal thyrocyte progenitors. Indeed, conditional ablation of Fgf8 in Tbx1-expressing cells caused an early thyroid phenotype similar to that of Tbx1 mutant mice. In addition, expression of an Fgf8 cDNA in the Tbx1 domain rescued the early size defect of the thyroid primordium in Tbx1 mutants. Thus, we have established that a Tbx1->Fgf8 pathway in the pharyngeal mesoderm is a key size regulator of mammalian thyroid.

Original languageEnglish
Pages (from-to)109-117
Number of pages9
JournalDevelopmental Biology
Volume328
Issue number1
DOIs
Publication statusPublished - Apr 1 2009

Keywords

  • Fgf8
  • Mouse
  • Tbx1
  • Thyroid development

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology
  • Molecular Biology

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