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Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision

  • Siew Cheng Phua
  • , Shuhei Chiba
  • , Masako Suzuki
  • , Emily Su
  • , Elle C. Roberson
  • , Ganesh V. Pusapati
  • , Mitsutoshi Setou
  • , Rajat Rohatgi
  • , Jeremy F. Reiter
  • , Koji Ikegami
  • , Takanari Inoue

Research output: Contribution to journalArticlepeer-review

Abstract

The life cycle of a primary cilium begins in quiescence and ends prior to mitosis. In quiescent cells, the primary cilium insulates itself from contiguous dynamic membrane processes on the cell surface to function as a stable signaling apparatus. Here, we demonstrate that basal restriction of ciliary structure dynamics is established by the cilia-enriched phosphoinositide 5-phosphatase, Inpp5e. Growth induction displaces ciliary Inpp5e and accumulates phosphatidylinositol 4,5-bisphosphate in distal cilia. This change triggers otherwise-forbidden actin polymerization in primary cilia, which excises cilia tips in a process we call cilia decapitation. While cilia disassembly is traditionally thought to occur solely through resorption, we show that an acute loss of IFT-B through cilia decapitation precedes resorption. Finally, we propose that cilia decapitation induces mitogenic signaling and constitutes a molecular link between the cilia life cycle and cell-division cycle. This newly defined ciliary mechanism may find significance in cell proliferation control during normal development and cancer.

Original languageEnglish (US)
Pages (from-to)264-279.e15
JournalCell
Volume168
Issue number1-2
DOIs
StatePublished - Jan 12 2017

Keywords

  • AurA
  • F-actin
  • Gli
  • Inpp5e
  • PI(4,5)P
  • Primary cilia
  • cell-cycle entry
  • decapitation
  • disassembly
  • ectosome
  • extracellular vesicles
  • genetically encoded ciliary actin inhibitor

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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