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Cortical excitability and cell division.
Michaud, Ani; Swider, Zachary T; Landino, Jennifer; Leda, Marcin; Miller, Ann L; von Dassow, George; Goryachev, Andrew B; Bement, William M.
Affiliation
  • Michaud A; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA; Center for Quantitative Cell Imaging, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA.
  • Swider ZT; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA; Center for Quantitative Cell Imaging, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA.
  • Landino J; Department of Molecular, Cellular, and Developmental Biology, University of Michigan-Ann Arbor, 5264 Biological Sciences Building, 1105 North University Avenue, Ann Arbor, MI 48109-1085, USA.
  • Leda M; Centre for Synthetic and Systems Biology, University of Edinburgh, 2.03 C.H. Waddington Building, King's Buildings, University of Edinburgh, Max Born Crescent, Edinburgh EH9 3BF, UK.
  • Miller AL; Department of Molecular, Cellular, and Developmental Biology, University of Michigan-Ann Arbor, 5264 Biological Sciences Building, 1105 North University Avenue, Ann Arbor, MI 48109-1085, USA.
  • von Dassow G; Oregon Institute of Marine Biology, University of Oregon, 63466 Boat Basin Road, Charleston, OR 97420, USA.
  • Goryachev AB; Centre for Synthetic and Systems Biology, University of Edinburgh, 2.03 C.H. Waddington Building, King's Buildings, University of Edinburgh, Max Born Crescent, Edinburgh EH9 3BF, UK.
  • Bement WM; Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA; Center for Quantitative Cell Imaging, University of Wisconsin-Madison, 1525 Linden Drive, Madison, WI 53706, USA; Department of Integrative Biology, University of Wisconsin-Ma
Curr Biol ; 31(10): R553-R559, 2021 05 24.
Article in En | MEDLINE | ID: mdl-34033789
ABSTRACT
As the interface between the cell and its environment, the cell cortex must be able to respond to a variety of external stimuli. This is made possible in part by cortical excitability, a behavior driven by coupled positive and negative feedback loops that generate propagating waves of actin assembly in the cell cortex. Cortical excitability is best known for promoting cell protrusion and allowing the interpretation of and response to chemoattractant gradients in migrating cells. It has recently become apparent, however, that cortical excitability is involved in the response of the cortex to internal signals from the cell-cycle regulatory machinery and the spindle during cell division. Two overlapping functions have been ascribed to cortical excitability in cell division control of cell division plane placement, and amplification of the activity of the small GTPase Rho at the equatorial cortex during cytokinesis. Here, we propose that cortical excitability explains several important yet poorly understood features of signaling during cell division. We also consider the potential advantages that arise from the use of cortical excitability as a signaling mechanism to regulate cortical dynamics in cell division.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Actins / Cytokinesis Language: En Journal: Curr Biol Journal subject: BIOLOGIA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Actins / Cytokinesis Language: En Journal: Curr Biol Journal subject: BIOLOGIA Year: 2021 Type: Article Affiliation country: United States