Recycling limits the lifetime of actin turnover

Intracellular organization is largely mediated by the actin turnover. Cellular actin networks consume matter and energy to sustain their dynamics, while maintaining their appearance. This behavior, called ‘dynamic steady state’, enables cells to sense and adapt to their environment. However, how structural stability can be maintained during the constant turnover of a limited actin monomer pool is poorly understood. To answer this question, we developed an experimental system using actin bead motility in a compartment with a limited amount of monomer. We used the speed and the size of the actin comet tails to evaluate the system’s monomer consumption and its lifetime. We established the relative contribution of actin assembly, disassembly and recycling for a bead movement over tens of hours. Recycling mediated by cyclase-associated proteins is the key step in allowing the reuse of monomers for multiple assembly cycles. Energy supply and protein aging are also factors that limit the lifetime of actin turnover. This work reveals the balancing mechanism for long-term network assembly with a limited amount of building blocks.

[1]  P. Lappalainen,et al.  Biochemical and mechanical regulation of actin dynamics , 2022, Nature Reviews Molecular Cell Biology.

[2]  L. Blanchoin,et al.  Actin network architecture can ensure robust centering or sensitive decentering of the centrosome , 2022, The EMBO journal.

[3]  Romain F. Laine,et al.  TrackMate 7: integrating state-of-the-art segmentation algorithms into tracking pipelines , 2022, Nature Methods.

[4]  A. Echard,et al.  Oxidation and reduction of actin: Origin, impact in vitro and functional consequences in vivo. , 2022, European journal of cell biology.

[5]  A. Bausch,et al.  Activity-induced polar patterns of filaments gliding on a sphere , 2022, Nature Communications.

[6]  T. Glonek,et al.  Intracellular ATP Concentration and Implication for Cellular Evolution , 2021, Biology.

[7]  A. Bershadsky,et al.  Crosstalk between myosin II and formin functions in the regulation of force generation and actomyosin dynamics in stress fibers , 2021, bioRxiv.

[8]  C. Gregorio,et al.  Redefining actin dynamics of the pointed-end complex in striated muscle. , 2021, Trends in cell biology.

[9]  P. R. ten Wolde,et al.  Cross-linkers at growing microtubule ends generate forces that drive actin transport , 2021, bioRxiv.

[10]  H. Higgs,et al.  Multiple roles for actin in secretory and endocytic pathways , 2021, Current Biology.

[11]  U. Endesfelder,et al.  Mutual functional dependence of cyclase-associated protein 1 (CAP1) and cofilin1 in neuronal actin dynamics and growth cone function , 2021, Progress in Neurobiology.

[12]  Y. Samstag,et al.  Redox Regulation of the Actin Cytoskeleton in Cell Migration and Adhesion: On the Way to a Spatiotemporal View , 2021, Frontiers in Cell and Developmental Biology.

[13]  G. Papoian,et al.  Different translation dynamics of β- and γ-actin regulates cell migration , 2021, bioRxiv.

[14]  Glen M. Hocky,et al.  Actin crosslinker competition and sorting drive emergent GUV size-dependent actin network architecture , 2020, Communications Biology.

[15]  E. Marcello,et al.  CAPt’n of Actin Dynamics: Recent Advances in the Molecular, Developmental and Physiological Functions of Cyclase-Associated Protein (CAP) , 2020, Frontiers in Cell and Developmental Biology.

[16]  J. Grantham The Molecular Chaperone CCT/TRiC: An Essential Component of Proteostasis and a Potential Modulator of Protein Aggregation , 2020, Frontiers in Genetics.

[17]  M. Gardel,et al.  The Actin Cytoskeleton as an Active Adaptive Material. , 2020, Annual review of condensed matter physics.

[18]  S. Shekhar,et al.  Genetically inspired in vitro reconstitution of Saccharomyces cerevisiae actin cables from seven purified proteins , 2020, Molecular biology of the cell.

[19]  Haiyang Jia,et al.  Bottom-up synthetic biology: reconstitution in space and time. , 2019, Current opinion in biotechnology.

[20]  J. Kondev,et al.  Synergy between Cyclase-associated protein and Cofilin accelerates actin filament depolymerization by two orders of magnitude , 2019, Nature Communications.

[21]  I. Vattulainen,et al.  Mechanism of synergistic actin filament pointed end depolymerization by cyclase-associated protein and cofilin , 2019, Nature Communications.

[22]  R. Vincentelli,et al.  Sizes of actin networks sharing a common environment are determined by the relative rates of assembly , 2019, PLoS biology.

[23]  A. Mogilner,et al.  Quantitative regulation of the dynamic steady state of actin networks , 2019, eLife.

[24]  L. Blanchoin,et al.  Dynamic stability of the actin ecosystem , 2018, Journal of Cell Science.

[25]  L. Blanchoin,et al.  Actin-Network Architecture Regulates Microtubule Dynamics , 2018, Current Biology.

[26]  A. Mogilner,et al.  Scaling behaviour in steady-state contracting actomyosin networks , 2018, Nature Physics.

[27]  I. Vattulainen,et al.  Structural basis of actin monomer re-charging by cyclase-associated protein , 2018, Nature Communications.

[28]  Sonal,et al.  Myosin-II activity generates a dynamic steady state with continuous actin turnover in a minimal actin cortex , 2018, Journal of Cell Science.

[29]  A. Mogilner,et al.  Actin Turnover in Lamellipodial Fragments , 2017, Current Biology.

[30]  C. Schmeiser,et al.  Load Adaptation of Lamellipodial Actin Networks , 2017, Cell.

[31]  Y. Senju,et al.  ADF/Cofilin Accelerates Actin Dynamics by Severing Filaments and Promoting Their Depolymerization at Both Ends , 2017, Current Biology.

[32]  B. Goode,et al.  Accelerated actin filament polymerization from microtubule plus ends , 2016, Science.

[33]  G. Charras,et al.  Actin kinetics shapes cortical network structure and mechanics , 2016, Science Advances.

[34]  Tzer Han Tan,et al.  Self-organized stress patterns drive state transitions in actin cortices , 2016, Science Advances.

[35]  R. Krishnan,et al.  Generation of contractile actomyosin bundles depends on mechanosensitive actin filament assembly and disassembly , 2015, eLife.

[36]  Matthieu Piel,et al.  Innate control of actin nucleation determines two distinct migration behaviours in dendritic cells , 2015, Nature Cell Biology.

[37]  L. Blanchoin,et al.  Architecture Dependence of Actin Filament Network Disassembly , 2015, Current Biology.

[38]  Eric A. Vitriol,et al.  Two functionally distinct sources of actin monomers supply the leading edge of lamellipodia. , 2015, Cell reports.

[39]  S. Ishiwata,et al.  Cell-sized spherical confinement induces the spontaneous formation of contractile actomyosin rings in vitro , 2015, Nature Cell Biology.

[40]  D. Kovar,et al.  Profilin regulates F-actin network homeostasis by favoring formin over Arp2/3 complex. , 2015, Developmental cell.

[41]  M. Steinmetz,et al.  Actin–microtubule coordination at growing microtubule ends , 2014, Nature Communications.

[42]  L. Blanchoin,et al.  Autonomous and in trans functions for the two halves of Srv2/CAP in promoting actin turnover , 2014, Cytoskeleton.

[43]  J. Alvarado,et al.  Alignment of nematic and bundled semiflexible polymers in cell-sized confinement. , 2014, Soft matter.

[44]  Eric A. Vitriol,et al.  Instantaneous inactivation of cofilin reveals its function of F-actin disassembly in lamellipodia , 2013, Molecular biology of the cell.

[45]  N. Watanabe,et al.  Can filament treadmilling alone account for the F‐actin turnover in lamellipodia? , 2013, Cytoskeleton.

[46]  G. Charras,et al.  Analysis of turnover dynamics of the submembranous actin cortex , 2013, Molecular biology of the cell.

[47]  N. Watanabe,et al.  Distributed actin turnover in the lamellipodium and FRAP kinetics. , 2013, Biophysical journal.

[48]  D. Breitsprecher,et al.  Srv2/cyclase-associated protein forms hexameric shurikens that directly catalyze actin filament severing by cofilin , 2013, Molecular biology of the cell.

[49]  O. Micheau,et al.  Small heat shock proteins and the cytoskeleton: an essential interplay for cell integrity? , 2012, The international journal of biochemistry & cell biology.

[50]  W. Marshall,et al.  How Cells Know the Size of Their Organelles , 2012, Science.

[51]  L. Blanchoin,et al.  How actin network dynamics control the onset of actin-based motility , 2012, Proceedings of the National Academy of Sciences.

[52]  W. Brieher,et al.  Cyclase-associated Protein (CAP) Acts Directly on F-actin to Accelerate Cofilin-mediated Actin Severing across the Range of Physiological pH* , 2012, The Journal of Biological Chemistry.

[53]  Charles Kervrann,et al.  Confinement induces actin flow in a meiotic cytoplasm , 2012, Proceedings of the National Academy of Sciences.

[54]  A. Cardona,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[55]  M. Fermigier,et al.  Impact of branching on the elasticity of actin networks , 2012, Proceedings of the National Academy of Sciences.

[56]  Manuel Théry,et al.  Actin Network Architecture Can Determine Myosin Motor Activity , 2012, Science.

[57]  A. Hyman,et al.  Organelle Growth Control through Limiting Pools of Cytoplasmic Components , 2012, Current Biology.

[58]  Frederick S. Soo,et al.  Choosing orientation: influence of cargo geometry and ActA polarization on actin comet tails , 2012, Molecular biology of the cell.

[59]  J. Alvarado,et al.  Self-organized patterns of actin filaments in cell-sized confinement , 2011 .

[60]  K. Rottner,et al.  Actin dynamics and turnover in cell motility. , 2011, Current opinion in cell biology.

[61]  L. Blanchoin,et al.  Turnover of branched actin filament networks by stochastic fragmentation with ADF/cofilin , 2011, Molecular biology of the cell.

[62]  B. Haarer,et al.  Diverse protective roles of the actin cytoskeleton during oxidative stress , 2011, Cytoskeleton.

[63]  Suliana Manley,et al.  A role for actin arcs in the leading-edge advance of migrating cells , 2011, Nature Cell Biology.

[64]  Alfred Nordheim,et al.  Linking actin dynamics and gene transcription to drive cellular motile functions , 2010, Nature Reviews Molecular Cell Biology.

[65]  D. Drubin,et al.  Loss of Aip1 reveals a role in maintaining the actin monomer pool and an in vivo oligomer assembly pathway , 2010, The Journal of cell biology.

[66]  W. Marshall,et al.  Building the cell: design principles of cellular architecture , 2008, Nature Reviews Molecular Cell Biology.

[67]  R. Mullins,et al.  Capping Protein Increases the Rate of Actin-Based Motility by Promoting Filament Nucleation by the Arp2/3 Complex , 2008, Cell.

[68]  Klemens Rottner,et al.  Arp2/3 complex interactions and actin network turnover in lamellipodia , 2008, The EMBO journal.

[69]  H. Higgs,et al.  The many faces of actin: matching assembly factors with cellular structures , 2007, Nature Cell Biology.

[70]  P. Nordlund,et al.  Molecular and Structural Basis for Redox Regulation of β-Actin , 2007 .

[71]  L. Blanchoin,et al.  Actin-Filament Stochastic Dynamics Mediated by ADF/Cofilin , 2007, Current Biology.

[72]  E. Andrianantoandro,et al.  Mechanism of actin filament turnover by severing and nucleation at different concentrations of ADF/cofilin. , 2006, Molecular cell.

[73]  P. Lappalainen,et al.  Stress fibers are generated by two distinct actin assembly mechanisms in motile cells , 2006, The Journal of cell biology.

[74]  P. Lappalainen,et al.  Regulation of cytoskeletal dynamics by actin-monomer-binding proteins. , 2004, Trends in cell biology.

[75]  P. Mattila,et al.  Cyclase-associated protein 1 (CAP1) promotes cofilin-induced actin dynamics in mammalian nonmuscle cells. , 2004, Molecular biology of the cell.

[76]  J. Bamburg,et al.  ADF/Cofilin Controls Cell Polarity during Fibroblast Migration , 2003, Current Biology.

[77]  Marie-France Carlier,et al.  The dynamics of actin-based motility depend on surface parameters , 2002, Nature.

[78]  Kenji Moriyama,et al.  Human CAP1 is a key factor in the recycling of cofilin and actin for rapid actin turnover. , 2002, Journal of cell science.

[79]  Timothy J Mitchison,et al.  Single-Molecule Speckle Analysis of Actin Filament Turnover in Lamellipodia , 2002, Science.

[80]  R. Rossi,et al.  The actin cytoskeleton response to oxidants: from small heat shock protein phosphorylation to changes in the redox state of actin itself. , 2001, Free radical biology & medicine.

[81]  J. Cooper,et al.  Interactions with PIP2, ADP-actin monomers, and capping protein regulate the activity and localization of yeast twinfilin , 2001, The Journal of cell biology.

[82]  Gary G. Borisy,et al.  Dendritic organization of actin comet tails , 2001, Current Biology.

[83]  Marie-France Carlier,et al.  Reconstitution of actin-based motility of Listeria and Shigella using pure proteins , 1999, Nature.

[84]  P. Sansonetti,et al.  Activation of the Cdc42 Effector N-Wasp by the Shigella flexneri Icsa Protein Promotes Actin Nucleation by Arp2/3 Complex and Bacterial Actin-Based Motility , 1999, The Journal of cell biology.

[85]  R. Colombo,et al.  The tert-butyl hydroperoxide-induced oxidation of actin Cys-374 is coupled with structural changes in distant regions of the protein. , 1999, Biochemistry.

[86]  T. Pollard,et al.  Mechanism of Interaction of Acanthamoeba Actophorin (ADF/Cofilin) with Actin Filaments* , 1999, The Journal of Biological Chemistry.

[87]  J A Theriot,et al.  Motility of ActA protein-coated microspheres driven by actin polymerization. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[88]  T. Pollard,et al.  Interaction of Actin Monomers with AcanthamoebaActophorin (ADF/Cofilin) and Profilin* , 1998, The Journal of Biological Chemistry.

[89]  T D Pollard,et al.  The interaction of Arp2/3 complex with actin: nucleation, high affinity pointed end capping, and formation of branching networks of filaments. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[90]  Jonathan M. Austyn,et al.  Dendritic cells , 1998, Current opinion in hematology.

[91]  P. Lappalainen,et al.  Cofilin promotes rapid actin filament turnover in vivo , 1997, Nature.

[92]  R. Colombo,et al.  H2O2-treated actin: assembly and polymer interactions with cross-linking proteins. , 1995, Biophysical journal.

[93]  P. Cossart,et al.  Actin-based movement of Listeria monocytogenes: actin assembly results from the local maintenance of uncapped filament barbed ends at the bacterium surface , 1995, The Journal of cell biology.

[94]  H. Isambert,et al.  Flexibility of actin filaments derived from thermal fluctuations. Effect of bound nucleotide, phalloidin, and muscle regulatory proteins , 1995, The Journal of Biological Chemistry.

[95]  T. Pollard,et al.  Nucleotide-free actin: stabilization by sucrose and nucleotide binding kinetics. , 1995, Biochemistry.

[96]  T. Pollard,et al.  Purification, characterization and crystallization of Acanthamoeba profilin expressed in Escherichia coli. , 1994, Journal of molecular biology.

[97]  Julie A. Theriot,et al.  The rate of actin-based motility of intracellular Listeria monocytogenes equals the rate of actin polymerization , 1992, Nature.

[98]  Julie A. Theriot,et al.  Actin microfilament dynamics in locomoting cells , 1991, Nature.

[99]  Y. Wang,et al.  Exchange of actin subunits at the leading edge of living fibroblasts: possible role of treadmilling , 1985, The Journal of cell biology.

[100]  J. Spudich,et al.  The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin. , 1971, The Journal of biological chemistry.

[101]  Laurent Blanchoin,et al.  Actin dynamics, architecture, and mechanics in cell motility. , 2014, Physiological reviews.

[102]  Gerald F. Joyce,et al.  CRAWLING TOWARD A UNIFIED MODEL OF CELL MOTILITY : Spatial and Temporal Regulation of Actin Dynamics , 2005 .

[103]  T. Pollard,et al.  Cellular Motility Driven by Assembly and Disassembly of Actin Filaments , 2003, Cell.

[104]  T D Pollard,et al.  Molecular mechanisms controlling actin filament dynamics in nonmuscle cells. , 2000, Annual review of biophysics and biomolecular structure.