Tubular clathrin/AP-2 lattices pinch collagen fibers to support 3D cell migration

被引:84
作者
Elkhatib, Nadia [1 ]
Bresteau, Enzo [1 ]
Baschieri, Francesco [1 ]
Rioja, Alba Lopez [1 ]
van Niel, Guillaume [2 ,4 ]
Vassilopoulos, Stephane [3 ]
Montagnac, Guillaume [1 ]
机构
[1] Univ Paris Saclay, Gustave Roussy Inst, INSERM, U1170, Villejuif, France
[2] Univ Rech Paris Sci & Lettres, Inst Curie, Ctr Univ, UMR144, Paris, France
[3] Univ Paris 06, INSERM, UMR S974, Inst Myol, Paris, France
[4] Univ Paris, INSERM, Ctr Psychiat & Neurosci, U894, Paris, France
关键词
ENDOCYTIC TRAFFICKING; DEPENDENT ENDOCYTOSIS; ADHESIONS; DYNAMICS; EXOCYTOSIS; INTEGRINS; DAB2;
D O I
10.1126/science.aal4713
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Migrating cells often use focal adhesions in order to move. Focal adhesions are less prominent in cells migrating in three-dimensional (3D) as compared with 2D environments. We looked for alternative adhesion structures supporting cell migration. We analyzed the dynamics of clathrin-coated pits in cells migrating in a 3D environment of collagen fibers. Both topological cues and local engagement of integrins triggered the accumulation of clathrin-coated structures on fibers. Clathrin/adaptor protein 2 (AP-2) lattices pinched collagen fibers by adopting a tube-like morphology and regulated adhesion to fibers in an endocytosis-independent manner. During migration, tubular clathrin/AP-2 lattices stabilized cellular protrusions by providing anchoring points to collagen fibers. Thus, tubular clathrin/AP-2 lattices promote cell adhesion that, in coordination with focal adhesions, supports cell migration in 3D.
引用
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页数:8
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