Guidance and activation of murine macrophages by nanometric scale topography

被引:276
作者
WojciakStothard, B [1 ]
Curtis, A [1 ]
Monaghan, W [1 ]
Macdonald, K [1 ]
Wilkinson, C [1 ]
机构
[1] UNIV GLASGOW,DEPT ELECTR & ELECT ENGN,GLASGOW G12 8QQ,LANARK,SCOTLAND
基金
英国惠康基金;
关键词
D O I
10.1006/excr.1996.0098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied the guidance and activation of macrophages from the P388D1 cell line and rat peritoneum by topographic features on a nanometric scale, Cells were plated on plain fused silica substrata or substrata with microfabricated grooves and steps, 30-282 nm deep, The contact of cells with the patterned surface activated cell spreading and adhesion and increased the number of protrusions of the cell membrane. These changes were accompanied by an increase in the amount of F-actin in cells, The accumulation of F-actin and vinculin in cells was observed along the edges of single steps or grooves, Formation of focal contacts along discontinuities in the substratum was accompanied by the phosphorylation of tyrosine colocalized with F-actin and vinculin, A similar pattern of staining was seen in cells stained for vitronectin receptor, alpha V integrin, but not for integrins alpha 5 beta 1 or alpha 3 beta 1, Cells cultured on nanogrooves showed a higher phagocytotic activity than cells cultured on plain substrata, We show that macrophages can react to ultrafine features of topography of a size comparable to that of a single collagen fiber and become activated by the contact with topographic features. (C) 1996 Academic Press, Inc.
引用
收藏
页码:426 / 435
页数:10
相关论文
共 25 条
[1]   CONNECTIVE-TISSUE PROTEINS AND PHAGOCYTIC CELL-FUNCTION - LAMININ ENHANCES COMPLEMENT AND FC-MEDIATED PHAGOCYTOSIS BY CULTURED HUMAN MACROPHAGES [J].
BOHNSACK, JF ;
KLEINMAN, HK ;
TAKAHASHI, T ;
OSHEA, JJ ;
BROWN, EJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (05) :912-923
[4]   ONCOGENES AND SIGNAL TRANSDUCTION [J].
CANTLEY, LC ;
AUGER, KR ;
CARPENTER, C ;
DUCKWORTH, B ;
GRAZIANI, A ;
KAPELLER, R ;
SOLTOFF, S .
CELL, 1991, 64 (02) :281-302
[5]  
CHOU LS, 1995, J CELL SCI, V108, P1563
[6]  
CLARK P, 1990, DEVELOPMENT, V108, P635
[7]  
CLARK P, 1991, J CELL SCI, V99, P73
[8]  
CURTIS ASG, 1990, CRIT REV BIOCOMPAT, V5, P343
[9]  
CURTIS ASG, 1995, IN PRESS CELL ENG IN
[10]  
DUNN GA, 1986, J CELL SCI, V83, P313