Free Edges in Epithelial Cell Sheets Stimulate Epidermal Growth Factor Receptor Signaling

被引:24
作者
Block, Ethan R. [1 ]
Tolino, Michael A. [1 ]
Lozano, Jennifer S. [1 ]
Lathrop, Kira L. [1 ]
Sullenberger, Rebecca S. [1 ]
Mazie, Abigail R. [1 ]
Klarlund, Jes K. [1 ]
机构
[1] Univ Pittsburgh, Inst Eye & Ear, Ophthalmol & Visual Sci Res Ctr, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
EGF RECEPTOR; KERATINOCYTE MIGRATION; CONNEXIN HEMICHANNELS; EXTRACELLULAR-MATRIX; ACTIVATION; REPAIR; KINASE; MECHANOTRANSDUCTION; EXPRESSION; PROTEIN;
D O I
10.1091/mbc.E09-12-1026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability of epithelia to migrate and cover wounds is essential to maintaining their functions as physical barriers. Wounding induces many cues that may affect the transition to motility, including the immediate mechanical perturbation, release of material from broken cells, new interactions with adjacent extracellular matrix, and breakdown of physical separation of ligands from their receptors. Depending on the exact nature of wounds, some cues may be present only transiently or insignificantly. In many epithelia, activation of the epidermal growth factor receptor (EGFR) is a central event in induction of motility, and we find that its continuous activation is required for progression of healing of wounds in sheets of corneal epithelial cells. Here, we examine the hypothesis that edges, which are universally and continuously present in wounds, are a cue. Using a novel culture model we find that their presence is sufficient to cause activation of the EGFR and increased motility of cells in the absence of other cues. Edges that are bordered by agarose do not induce activation of the EGFR, indicating that activation is not due to loss of any specific type of cell-cell interaction but rather due to loss of physical constraints.
引用
收藏
页码:2172 / 2181
页数:10
相关论文
共 74 条
[1]   CONTACT INHIBITION AND MALIGNANCY [J].
ABERCROMBIE, M .
NATURE, 1979, 281 (5729) :259-262
[2]   Sheet migration by wounded monolayers as an emergent property of single-cell dynamics [J].
Bindschadler, Michael ;
McGrath, James L. .
JOURNAL OF CELL SCIENCE, 2007, 120 (05) :876-884
[3]   Gelatinase-mediated migration and invasion of cancer cells [J].
Björklund, M ;
Koivunen, E .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2005, 1755 (01) :37-69
[4]   Wounding induces motility in sheets of corneal epithelial cells through loss of spatial constraints - Role of heparin-binding epidermal growth factor-like growth factor signaling [J].
Block, ER ;
Matela, AR ;
SundarRaj, N ;
Iszkula, ER ;
Klarlund, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24307-24312
[5]   Wounding Sheets of Epithelial Cells Activates the Epidermal Growth Factor Receptor through Distinct Short- and Long-Range Mechanisms [J].
Block, Ethan R. ;
Klarlund, Jes K. .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (11) :4909-4917
[6]   Injury and nucleotides induce phosphorylation of epidermal growth factor receptor: MMP and HB-EGF dependent pathway [J].
Boucher, Ilene ;
Yang, LingLing ;
Mayo, Courtney ;
Klepeis, Veronica ;
Trinkaus-Randall, Vickery .
EXPERIMENTAL EYE RESEARCH, 2007, 85 (01) :130-141
[7]   Ki67 protein: the immaculate deception? [J].
Brown, DC ;
Gatter, KC .
HISTOPATHOLOGY, 2002, 40 (01) :2-11
[8]   Integrin regulation of epidermal growth factor (EGF) receptor and of EGF-dependent responses [J].
Cabodi, S ;
Moro, L ;
Bergatto, E ;
Erba, EB ;
Di Stefano, P ;
Turco, E ;
Tarone, G ;
Defilippi, P .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2004, 32 :438-442
[9]   Force propagation across cells: mechanical coherence of dynamic cytoskeletons [J].
Cai, Yunfei ;
Sheetz, Michael P. .
CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (01) :47-50
[10]   Contact inhibition of locomotion in vivo controls neural crest directional migration [J].
Carmona-Fontaine, Carlos ;
Matthews, Helen K. ;
Kuriyama, Sei ;
Moreno, Mauricio ;
Dunn, Graham A. ;
Parsons, Maddy ;
Stern, Claudio D. ;
Mayor, Roberto .
NATURE, 2008, 456 (7224) :957-961