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
[11]   MicroRNA-30a inhibits cell migration and invasion by downregulating vimentin expression and is a potential prognostic marker in breast cancer [J].
Cheng, Chun-Wen ;
Wang, Hsiao-Wei ;
Chang, Chia-Wei ;
Chu, Hou-Wei ;
Chen, Cheng-You ;
Yu, Jyh-Cherng ;
Chao, Jui-I ;
Liu, Huei-Fang ;
Ding, Shian-ling ;
Shen, Chen-Yang .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 134 (03) :1081-1093
[12]  
Chu YW, 1996, AM J PATHOL, V148, P63
[13]   EXPRESSION OF COMPLETE KERATIN FILAMENTS IN MOUSE L-CELLS AUGMENTS CELL-MIGRATION AND INVASION [J].
CHU, YW ;
RUNYAN, RB ;
OSHIMA, RG ;
HENDRIX, MJC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) :4261-4265
[14]   Identification of Novel Interaction between Annexin A2 and Keratin 17 EVIDENCE FOR RECIPROCAL REGULATION [J].
Chung, Byung-Min ;
Murray, Christopher I. ;
Van Eyk, Jennifer E. ;
Coulombe, Pierre A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (10) :7573-7581
[15]   EXPRESSION OF VIMENTIN INTERMEDIATE FILAMENT CYTOSKELETON IN ACUTE NONLYMPHOBLASTIC LEUKEMIAS [J].
DELLAGI, K ;
TABILIO, A ;
PORTIER, MM ;
VAINCHENKER, W ;
CASTAIGNE, S ;
GUICHARD, J ;
BRETONGORIUS, J ;
BROUET, JC .
BLOOD, 1985, 65 (06) :1444-1452
[16]  
Deng M, 2012, ONCOGENE
[17]   Keratin 17 promotes epithelial proliferation and tumor growth by polarizing the immune response in skin [J].
DePianto, Daryle ;
Kerns, Michelle L. ;
Dlugosz, Andrzej A. ;
Coulombe, Pierre A. .
NATURE GENETICS, 2010, 42 (10) :910-+
[18]   Desmosomes at a glance [J].
Desai, Bhushan V. ;
Harmon, Robert M. ;
Green, Kathleen J. .
JOURNAL OF CELL SCIENCE, 2009, 122 (24) :4401-4407
[19]   Cytoplasmic intermediate filaments mediate actin-driven positioning of the nucleus [J].
Dupin, Isabelle ;
Sakamoto, Yasuhisa ;
Etienne-Manneville, Sandrine .
JOURNAL OF CELL SCIENCE, 2011, 124 (06) :865-872
[20]  
Eckes B, 1998, J CELL SCI, V111, P1897