| Literature DB >> 28086093 |
Siew Cheng Phua1, Shuhei Chiba2, Masako Suzuki3, Emily Su4, Elle C Roberson5, Ganesh V Pusapati6, Stéphane Schurmans, Mitsutoshi Setou7, Rajat Rohatgi6, Jeremy F Reiter5, Koji Ikegami8, Takanari Inoue9.
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.Entities:
Keywords: AurA; F-actin; Gli; Inpp5e; PI(4,5)P(2); Primary cilia; cell-cycle entry; decapitation; disassembly; ectosome; extracellular vesicles; genetically encoded ciliary actin inhibitor
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Year: 2017 PMID: 28086093 PMCID: PMC5660509 DOI: 10.1016/j.cell.2016.12.032
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582