Abstract

Cycling cells maintain centriole number at precisely two per cell in part by limiting their duplication to S phase under the control of the cell cycle machinery. In contrast, postmitotic multiciliated cells (MCCs) uncouple centriole assembly from cell cycle progression and produce hundreds of centrioles in the absence of DNA replication to serve as basal bodies for motile cilia. Although some cell cycle regulators have previously been implicated in motile ciliogenesis, how the cell cycle machinery is employed to amplify centrioles is unclear. We use transgenic mice and primary airway epithelial cell culture to show that Cdk2, the kinase responsible for the G1 to S phase transition, is also required in MCCs to initiate motile ciliogenesis. While Cdk2 is coupled with cyclins E and A2 during cell division, cyclin A1 is required during ciliogenesis, contributing to an alternative regulatory landscape that facilitates centriole amplification without DNA replication.

Highlights

  • Untreated air-liquid interface (ALI) + 4 d cells are robustly ciliating, but NU6140 treatment blocks all signs of motile ciliogenesis

  • Levels were normalized to Gapdh expression and compared to values obtained for MTECs at ALI-1d (n.d. = none detected). n.s., not significant, *p

  • 10 mm. (B) MTECs were treated with NU6140 from ALI + 0 to 4d

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Summary

Introduction

Untreated ALI + 4 d cells are robustly ciliating, but NU6140 treatment blocks all signs of motile ciliogenesis. MCC fate determination and motile ciliogenesis occur asynchronously, but early ALI culture days are strongly enriched for young MCCs at the early stages of the pathway and by ALI + 14 days the filter contains only mature MCCs. The immunofluorescence image shows centrioles in both MCCs and nonMCCs in green and cell boundaries in red. Mcidas, but not GFP, Foxj1 or Myb expression can drive the complete motile ciliogenesis pathway

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