Macrophages influence a competition of contact guidance and chemotaxis for fibroblast alignment in a fibrin gel coculture assay

被引:20
作者
Bromberek, BA
Enever, PAJ
Shreiber, DI
Caldwell, MD
Tranquillo, RT
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Surg, Minneapolis, MN 55455 USA
关键词
coculture assay; wound healing; fibroblasts; macrophages; fibrin gel; contact guidance; chemotaxis;
D O I
10.1006/excr.2002.5481
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rat dermal fibroblasts were dispersed initially in the outer shell of a fibrin gel sphere, while the inner core either was devoid of cells or contained peritoneal exudate cells (primarily macrophages), thereby mimicking the inflammatory phase of wound healing. The fibroblasts compacted floating fibrin microspheres over time. In the absence of macrophages, the initial distribution of fibroblasts (only in the shell) induced circumferential alignment of fibrin fibrils via compaction of the shell relative to the core. The aligned fibrils created a contact guidance field, which was manifested by strong circumferential alignment of the fibroblasts. However, in the presence of macrophages, the fibroblasts exhibited more radial alignment despite the simultaneous contact guidance field in the circumferential direction associated with compaction. This was attributed to a chemotactic gradient emanating from the core due to a putative factor(s) released by the macrophages. The presence of a radial chemotactic stimulus was supported by the finding of even greater radial alignment when fibrin microspheres were embedded in an agarose-fibrin gel that abolished compaction and consequently the contact guidance field. Our assay permits the simulation of tissue morphogenetic processes that involve cell guidance phenomena and tractional restructuring of the extracellular matrix. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:230 / 242
页数:13
相关论文
共 36 条
[11]  
DVORAK HF, 1986, NEW ENGL J MED, V315, P1650
[12]   CELL LOCOMOTION FORCES VERSUS CELL CONTRACTION FORCES FOR COLLAGEN LATTICE CONTRACTION - AN INVITRO MODEL OF WOUND CONTRACTION [J].
EHRLICH, HP ;
RAJARATNAM, JBM .
TISSUE & CELL, 1990, 22 (04) :407-417
[13]  
Freshney R.A., 1987, CULTURE ANIMAL CELLS, VSecond
[14]   THE ROLE OF EXTRACELLULAR-MATRIX IN THE MIGRATION AND DIFFERENTIATION OF PARIETAL ENDODERM FROM TERATOCARCINOMA EMBRYOID BODIES [J].
GRABEL, LB ;
WATTS, TD .
JOURNAL OF CELL BIOLOGY, 1987, 105 (01) :441-448
[15]  
Greiling D, 1997, J CELL SCI, V110, P861
[16]  
GRINNELL F, 1984, J CELL SCI, V66, P51
[17]   FIBROBLASTS, MYOFIBROBLASTS, AND WOUND CONTRACTION [J].
GRINNELL, F .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :401-404
[18]  
Guyton AC, 1991, TXB MED PHYSL
[19]   Estimation of cell traction and migration in an isometric cell traction assay [J].
Knapp, DM ;
Tower, TT ;
Tranquillo, RT ;
Barocas, VH .
AICHE JOURNAL, 1999, 45 (12) :2628-2640
[20]   A fibrin or collagen gel assay for tissue cell chemotaxis: Assessment of fibroblast chemotaxis to GRGDSP [J].
Knapp, DM ;
Helou, EF ;
Tranquillo, RT .
EXPERIMENTAL CELL RESEARCH, 1999, 247 (02) :543-553