Directed cytoskeleton self-organization

被引:100
作者
Vignaud, Timothee [1 ]
Blanchoin, Laurent [1 ]
Thery, Manuel [1 ]
机构
[1] CNRS UJF INRA CEA, Lab Physiol Cellulaire & Vegetale, Inst Rech Technol & Sci Vivant, F-38054 Grenoble, France
关键词
actin; microtubule; architecture; polarity; microfabrication; micropatterning; ACTIN-BASED MOTILITY; MITOTIC SPINDLE; CELL POLARITY; SPATIAL-ORGANIZATION; MICROTUBULE ASTERS; SYMMETRY-BREAKING; ARP2/3; COMPLEX; SHAPE; ORIENTATION; GEOMETRY;
D O I
10.1016/j.tcb.2012.08.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cytoskeleton architecture supports many cellular functions. Cytoskeleton networks form complex intracellular structures that vary during the cell cycle and between different cell types according to their physiological role. These structures do not emerge spontaneously. They result from the interplay between intrinsic self-organization properties and the conditions imposed by spatial boundaries. Along these boundaries, cytoskeleton filaments are anchored, repulsed, aligned, or reoriented. Such local effects can propagate altorations throughout the network and guide cytoskeleton assembly over relatively large distances. The experimental manipulation of spatial boundaries using microfabrication methods has revealed the underlying physical processes directing cytoskeleton self-organization. Here we review, step-by-step, from molecules to tissues, how the rules that govern assembly have been identified. We describe how complementary approaches, all based on controlling geometric conditions, from in vitro reconstruction to in vivo observation, shed new light on these fundamental organizing principles.
引用
收藏
页码:671 / 682
页数:12
相关论文
共 97 条
[1]   A "Primer"-Based Mechanism Underlies Branched Actin Filament Network Formation and Motility [J].
Achard, Verane ;
Martiel, Jean-Louis ;
Michelot, Alphee ;
Guerin, Christophe ;
Reymann, Anne-Cecile ;
Blanchoin, Laurent ;
Boujemaa-Paterski, Rajaa .
CURRENT BIOLOGY, 2010, 20 (05) :423-428
[2]   THE CORTICAL ACTOMYOSIN SYSTEM OF CYTOCHALASIN D-TREATED LYMPHOBLASTS [J].
BAILLY, E ;
CELATI, C ;
BORNENS, M .
EXPERIMENTAL CELL RESEARCH, 1991, 196 (02) :287-293
[3]  
Bergert M., 2012, P NATL ACAD SCI USA, V666, P1
[4]   The dynamics of actin-based motility depend on surface parameters [J].
Bernheim-Groswasser, A ;
Wiesner, S ;
Golsteyn, RM ;
Carlier, MF ;
Sykes, C .
NATURE, 2002, 417 (6886) :308-311
[5]   Mechanism of actin-based motility: A dynamic state diagram [J].
Bernheim-Groswasser, A ;
Prost, J ;
Sykes, C .
BIOPHYSICAL JOURNAL, 2005, 89 (02) :1411-1419
[6]   Filamentous network mechanics and active contractility determine cell and tissue shape [J].
Bischofs, Ilka B. ;
Klein, Franziska ;
Lehnert, Dirk ;
Bastmeyer, Martin ;
Schwarz, Ulrich S. .
BIOPHYSICAL JOURNAL, 2008, 95 (07) :3488-3496
[7]   THE CORTICAL MICROFILAMENT SYSTEM OF LYMPHOBLASTS DISPLAYS A PERIODIC OSCILLATORY ACTIVITY IN THE ABSENCE OF MICROTUBULES - IMPLICATIONS FOR CELL POLARITY [J].
BORNENS, M ;
PAINTRAND, M ;
CELATI, C .
JOURNAL OF CELL BIOLOGY, 1989, 109 (03) :1071-1083
[8]   Geometric determinants of directional cell motility revealed using microcontact printing [J].
Brock, A ;
Chang, E ;
Ho, CC ;
LeDuc, P ;
Jiang, XY ;
Whitesides, GM ;
Ingber, DE .
LANGMUIR, 2003, 19 (05) :1611-1617
[9]   Spatial segregation between cell-cell and cell-matrix adhesions [J].
Burute, Mithila ;
Thery, Manuel .
CURRENT OPINION IN CELL BIOLOGY, 2012, 24 (05) :628-636
[10]   N-cadherin expression level modulates integrin-mediated polarity and strongly impacts on the speed and directionality of glial cell migration [J].
Camand, Emeline ;
Peglion, Florent ;
Osmani, Nael ;
Sanson, Marc ;
Etienne-Manneville, Sandrine .
JOURNAL OF CELL SCIENCE, 2012, 125 (04) :844-857