Recycling of the actin monomer pool limits the lifetime of network turnover

被引:10
作者
Colin, Alexandra [1 ]
Kotila, Tommi [2 ,3 ]
Guerin, Christophe [1 ]
Orhant-Prioux, Magali [1 ]
Vianay, Benoit [4 ]
Mogilner, Alex [5 ,6 ]
Lappalainen, Pekka [2 ,3 ]
Thery, Manuel [1 ,4 ]
Blanchoin, Laurent [1 ,4 ]
机构
[1] Univ Grenoble Alpes, Interdisciplinary Res Inst Grenoble, CytoMorpho Lab, Lab Physiol Cellulaire & Vegetale,CEA,CNRS,INRA, Grenoble, France
[2] Univ Helsinki, Inst Biotechnol, Helsinki, Finland
[3] Univ Helsinki, Helsinki Inst Life Sci, Helsinki, Finland
[4] Univ Paris, Inst Rech St Louis, CytoMorpho Lab, Human Immunol Pathophysiol Immunotherapy HIPI U976, Paris, France
[5] NYU, Courant Inst Math Sci, New York, NY USA
[6] NYU, Dept Biol, New York, NY USA
基金
欧洲研究理事会; 芬兰科学院;
关键词
actin turnover; aging; lifetime; microwells; reconstituted system; ACANTHAMOEBA ACTOPHORIN ADF/COFILIN; F-ACTIN; FILAMENT TURNOVER; ARP2/3; COMPLEX; LEADING-EDGE; IN-VITRO; DYNAMICS; CELL; MOTILITY; COFILIN;
D O I
10.15252/embj.2022112717
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular organization is largely mediated by actin turnover. Cellular actin networks continuously assemble and disassemble, while maintaining their overall appearance. This behavior, called "dynamic steady state," allows 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 where polystyrene beads are propelled by an actin comet in a microwell containing a limited amount of components. 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 protein (CAP) is the key step in allowing the reuse of monomers for multiple assembly cycles. ATP 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.
引用
收藏
页数:20
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