4.3 Article

Notch signaling mediates olfactory multiciliated cell specification

Journal

CELLS & DEVELOPMENT
Volume 168, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.cdev.2021.203715

Keywords

Olfactory development; Multiciliated cell; Notch signaling; Cell fate specification

Funding

  1. National Institutes of Health [R01HD100023]
  2. NSF-Simons Center for Quantitative Biology at Northwestern University
  3. NSF-Simons MathBioSys Research Center (Simons Foundation/SFARI) [597491-RWC]
  4. National Science Foundation [1764421]

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This study in zebrafish identified the earliest time window of olfactory MCC differentiation, showing that OMCC cells derive from peridermal cells and are regulated by the Notch signaling pathway. The research also found regionally segregated Notch signaling regulates the number of OMCCs and the differentiation-associated genes during olfactory development.
Epithelial multiciliated cells (MCCs) use motile cilia to direct external fluid flow, the disruption of which is associated with human diseases in a broad array of organs such as those in the respiratory, reproductive, and renal systems. While many of the signaling pathways that regulate MCC formation in these organ systems have been identified, similar characterization of MCC differentiation in the developing olfactory system has been lacking. Here, using live cell tracking, targeted cell ablation, and temporally-specific inhibition of the Notch signaling pathway, we identify the earliest time window of zebrafish olfactory MCC (OMCC) differentiation and demonstrate these cells' derivation from peridermal cells. We also describe regionally segregated Notch signaling across time points of rapid OMCC differentiation and show that Notch signaling downregulation yields an increase in OMCCs, suggesting that OMCC fate is normally repressed in a region-specific manner during olfactory development. Finally, we describe Notch signaling's regulation of the differentiation/ciliogenesis-associated genes foxj1a and foxj1b. Taken together, these findings provide new insights into the origins and developmental programming of OMCCs in vivo.

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