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Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision.
Phua, Siew Cheng; Chiba, Shuhei; Suzuki, Masako; Su, Emily; Roberson, Elle C; Pusapati, Ganesh V; Schurmans, Stéphane; Setou, Mitsutoshi; Rohatgi, Rajat; Reiter, Jeremy F; Ikegami, Koji; Inoue, Takanari.
Afiliación
  • Phua SC; Department of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: phua0022@e.ntu.edu.sg.
  • Chiba S; Laboratory of Biological Science, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
  • Suzuki M; Advanced Research Facilities and Services, Preeminent Medical Photonics Education and Research Center, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
  • Su E; Department of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Roberson EC; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Pusapati GV; Departments of Medicine and Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Setou M; Department of Cellular and Molecular Anatomy and International Mass Imaging Center, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan.
  • Rohatgi R; Departments of Medicine and Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Reiter JF; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Ikegami K; Department of Cellular and Molecular Anatomy and International Mass Imaging Center, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan. Electronic address: kikegami@hama-med.ac.jp.
  • Inoue T; Department of Cell Biology and Center for Cell Dynamics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: jctinoue@jhmi.edu.
Cell ; 168(1-2): 264-279.e15, 2017 01 12.
Article en En | MEDLINE | ID: mdl-28086093
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.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ciclo Celular / Cilios Límite: Animals Idioma: En Revista: Cell Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ciclo Celular / Cilios Límite: Animals Idioma: En Revista: Cell Año: 2017 Tipo del documento: Article