β-Catenin signaling specifies progenitor cell identity in parallel with Shh signaling in the developing mammalian thalamus.

Krista K. Bluske, Tou Yia Vue, Yasuhiko Kawakami, Makoto M. Taketo, Kazuaki Yoshikawa, Jane E. Johnson, Yasushi Nakagawa

Research output: Contribution to journalArticle

32 Scopus citations

Abstract

Neural progenitor cells within the developing thalamus are spatially organized into distinct populations. Their correct specification is critical for generating appropriate neuronal subtypes in specific locations during development. Secreted signaling molecules, such as sonic hedgehog (Shh) and Wnts, are required for the initial formation of the thalamic primordium. Once thalamic identity is established and neurogenesis is initiated, Shh regulates the positional identity of thalamic progenitor cells. Although Wnt/β-catenin signaling also has differential activity within the thalamus during this stage of development, its significance has not been directly addressed. In this study, we used conditional gene manipulations in mice and explored the roles of β-catenin signaling in the regional identity of thalamic progenitor cells. We found β-catenin is required during thalamic neurogenesis to maintain thalamic fate while suppressing prethalamic fate, demonstrating that regulation of regional fate continues to require extrinsic signals. These roles of β-catenin appeared to be mediated at least partly by regulating two basic helix-loop-helix (bHLH) transcription factors, Neurog1 and Neurog2. β-Catenin and Shh signaling function in parallel to specify two progenitor domains within the thalamus, where individual transcription factors expressed in each progenitor domain were regulated differently by the two signaling pathways. We conclude that β-catenin has multiple functions during thalamic neurogenesis and that both Shh and β-catenin pathways are important for specifying distinct types of thalamic progenitor cells, ensuring that the appropriate neuronal subtypes are generated in the correct locations.

Original languageEnglish (US)
Pages (from-to)2692-2702
Number of pages11
JournalDevelopment (Cambridge, England)
Volume139
Issue number15
DOIs
Publication statusPublished - Aug 2012

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ASJC Scopus subject areas

  • Medicine(all)

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