Networking galore: intermediate filaments and cell migration

被引:146
作者
Chung, Byung-Min [1 ]
Rotty, Jeremy D. [1 ]
Coulombe, Pierre A. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
KERATIN FILAMENTS; EPITHELIAL-CELLS; DOWN-REGULATION; CANCER-CELLS; POSTTRANSLATIONAL MODIFICATIONS; EXPERIMENTAL COEXPRESSION; VIMENTIN CONTRIBUTES; INHIBITS GROWTH; SIZED FILAMENTS; EXPRESSION;
D O I
10.1016/j.ceb.2013.06.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intermediate filaments (IFs) are assembled from a diverse group of evolutionarily conserved proteins and are specified in a tissue-dependent, cell type-dependent, and context-dependent fashion in the body. IFs are involved in multiple cellular processes that are crucial for the maintenance of cell and tissue integrity and the response and adaptation to various stresses, as conveyed by the broad array of crippling clinical disorders caused by inherited mutations in IF coding sequences. Accordingly, the expression, assembly, and organization of IFs are tightly regulated. Migration is a fitting example of a cell-based phenomenon in which IFs participate as both effectors and regulators. With a particular focus on vimentin and keratin, we here review how the contributions of IFs to the cell's mechanical properties, to cytoarchitecture and adhesion, and to regulatory pathways collectively exert a significant impact on cell migration.
引用
收藏
页码:600 / 612
页数:13
相关论文
共 113 条
[21]   Expression of luminal and basal cytokeratins in human breast carcinoma [J].
El-Rehim, DMA ;
Pinder, SE ;
Paish, CE ;
Bell, J ;
Blamey, R ;
Robertson, JFR ;
Nicholson, RI ;
Ellis, IO .
JOURNAL OF PATHOLOGY, 2004, 203 (02) :661-671
[22]   Molecular phylogeny of metazoan intermediate filament proteins [J].
Erber, A ;
Riemer, D ;
Bovenschulte, M ;
Weber, K .
JOURNAL OF MOLECULAR EVOLUTION, 1998, 47 (06) :751-762
[23]   P2Y2 receptor inhibits EGF-induced MAPK pathway to stabilise keratinocyte hemidesmosomes [J].
Faure, Emilie ;
Garrouste, Francoise ;
Parat, Fabrice ;
Monferran, Sylvie ;
Leloup, Ludovic ;
Pommier, Gilbert ;
Kovacic, Herve ;
Lehmann, Maxime .
JOURNAL OF CELL SCIENCE, 2012, 125 (18) :4264-4277
[24]   Monitoring the Cytoskeletal EGF Response in Live Gastric Carcinoma Cells [J].
Felkl, Marco ;
Tomas, Kazmar ;
Smid, Matej ;
Mattes, Julian ;
Windoffer, Reinhard ;
Leube, Rudolf E. .
PLOS ONE, 2012, 7 (09)
[25]  
FLORENES VA, 1994, CANCER RES, V54, P354
[26]   Keratin 8 and 18 Loss in Epithelial Cancer Cells Increases Collective Cell Migration and Cisplatin Sensitivity through Claudin1 Up-regulation [J].
Fortier, Anne-Marie ;
Asselin, Eric ;
Cadrin, Monique .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (16) :11555-11571
[27]   PROTEIN COMPLEXES OF INTERMEDIATE-SIZED FILAMENTS - MELTING OF CYTOKERATIN COMPLEXES IN UREA REVEALS DIFFERENT POLYPEPTIDE SEPARATION CHARACTERISTICS [J].
FRANKE, WW ;
SCHILLER, DL ;
HATZFELD, M ;
WINTER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (23) :7113-7117
[28]   Nuclear mechanics during cell migration [J].
Friedl, Peter ;
Wolf, Katarina ;
Lammerding, Jan .
CURRENT OPINION IN CELL BIOLOGY, 2011, 23 (01) :55-64
[29]   Plasticity of cell migration: a multiscale tuning model [J].
Friedl, Peter ;
Wolf, Katarina .
JOURNAL OF CELL BIOLOGY, 2010, 188 (01) :11-19
[30]   EGF-induced MAPK Signaling Inhibits Hemidesmosome Formation through Phosphorylation of the Integrin β4 [J].
Frijns, Evelyne ;
Sachs, Norman ;
Kreft, Maaike ;
Wilhelmsen, Kevin ;
Sonnenberg, Arnoud .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (48) :37650-37662