4.7 Article

Epithelial stratification and placode invagination are separable functions in early morphogenesis of the molar tooth

Journal

DEVELOPMENT
Volume 143, Issue 4, Pages 670-681

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.130187

Keywords

Ectodermal organ; Morphogenesis; Placode; Invagination; Asymmetric cell division

Funding

  1. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/L002965/1]
  2. Biotechnology and Biological Sciences Research Council [BB/L002965/1, BB/E01335X/1] Funding Source: researchfish
  3. BBSRC [BB/E01335X/1, BB/L002965/1] Funding Source: UKRI

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Ectodermal organs, which include teeth, hair follicles, mammary ducts, and glands such as sweat, mucous and sebaceous glands, are initiated in development as placodes, which are epithelial thickenings that invaginate and bud into the underlying mesenchyme. These placodes are stratified into a basal and several suprabasal layers of cells. The mechanisms driving stratification and invagination are poorly understood. Using the mouse molar tooth as a model for ectodermal organ morphogenesis, we show here that vertical, stratifying cell divisions are enriched in the forming placode and that stratification is cell division dependent. Using inhibitor and gain-offunction experiments, we show that FGF signalling is necessary and sufficient for stratification but not invagination as such. We show that, instead, Shh signalling is necessary for, and promotes, invagination once suprabasal tissue is generated. Shh-dependent suprabasal cell shape suggests convergent migration and intercalation, potentially accounting for post-stratification placode invagination to bud stage. We present a model in which FGF generates suprabasal tissue by asymmetric cell division, while Shh triggers cell rearrangement in this tissue to drive invagination all the way to bud formation.

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