Literature DB >> 10320942

Cell migration as a five-step cycle.

M P Sheetz1, D Felsenfeld, C G Galbraith, D Choquet.   

Abstract

The migration of cells over substrata is a fundamental and critical function that requires the co-ordination of several cellular processes which operate in a cycle. At the level of the light microscope, the cycle can be divided into five steps: (1) extension of the leading edge; (2) adhesion to matrix contacts; (3) contraction of the cytoplasm; (4) release from contact sites; and (5) recycling of membrane receptors from the rear to the front of the cell. Each step is dependent upon one or more cyclical biochemical processes. The development of many in vitro and subcellular assays for the fundamental biochemical processes involved has increased our understanding of each cycle dramatically in the last several years to include a definition of many of the protein and enzymic components, the role of the position of extracellular-matrix receptors on the cell, and the contribution of physical force. The next generation of questions are directed at resolving the roles of the many individual proteins in each step of the cell migration process. In this chapter we will examine each of the migration steps and discuss the biochemical mechanisms that may underlie them.

Mesh:

Year:  1999        PMID: 10320942

Source DB:  PubMed          Journal:  Biochem Soc Symp        ISSN: 0067-8694


  65 in total

1.  Quantitative morphodynamics of endothelial cells within confluent cultures in response to fluid shear stress.

Authors:  P Dieterich; M Odenthal-Schnittler; C Mrowietz; M Krämer; L Sasse; H Oberleithner; H J Schnittler
Journal:  Biophys J       Date:  2000-09       Impact factor: 4.033

2.  Modulation of fibroblast morphology and adhesion during collagen matrix remodeling.

Authors:  Elisa Tamariz; Frederick Grinnell
Journal:  Mol Biol Cell       Date:  2002-11       Impact factor: 4.138

3.  The differential regulation of cell motile activity through matrix stiffness and porosity in three dimensional collagen matrices.

Authors:  Miguel Miron-Mendoza; Joachim Seemann; Frederick Grinnell
Journal:  Biomaterials       Date:  2010-09       Impact factor: 12.479

4.  Force-dependent integrin-cytoskeleton linkage formation requires downregulation of focal complex dynamics by Shp2.

Authors:  Götz von Wichert; Beatrice Haimovich; Gen-Sheng Feng; Michael P Sheetz
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

5.  Pyk2 regulates multiple signaling events crucial for macrophage morphology and migration.

Authors:  M Okigaki; C Davis; M Falasca; S Harroch; D P Felsenfeld; M P Sheetz; J Schlessinger
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-05       Impact factor: 11.205

Review 6.  Mathematical modeling of tumor-induced angiogenesis.

Authors:  Nikos V Mantzaris; Steve Webb; Hans G Othmer
Journal:  J Math Biol       Date:  2004-02-06       Impact factor: 2.259

7.  Rho mediates the shear-enhancement of endothelial cell migration and traction force generation.

Authors:  Yan-Ting Shiu; Song Li; William A Marganski; Shunichi Usami; Martin A Schwartz; Yu-Li Wang; Micah Dembo; Shu Chien
Journal:  Biophys J       Date:  2004-04       Impact factor: 4.033

8.  Roles of mechanical force and CXCR1/CXCR2 in shear-stress-induced endothelial cell migration.

Authors:  Ye Zeng; Yang Shen; Xian-Liang Huang; Xiao-Jing Liu; Xiao-Heng Liu
Journal:  Eur Biophys J       Date:  2011-10-12       Impact factor: 1.733

9.  Forming the cell rear first: breaking cell symmetry to trigger directed cell migration.

Authors:  Louise P Cramer
Journal:  Nat Cell Biol       Date:  2010-07       Impact factor: 28.824

10.  m-Calpain activation is regulated by its membrane localization and by its binding to phosphatidylinositol 4,5-bisphosphate.

Authors:  Ludovic Leloup; Hanshuang Shao; Yong Ho Bae; Bridget Deasy; Donna Stolz; Partha Roy; Alan Wells
Journal:  J Biol Chem       Date:  2010-08-20       Impact factor: 5.157

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