BASIC FIBROBLAST GROWTH-FACTOR IS A SIGNAL FOR THE INITIATION OF CENTROSOME REDISTRIBUTION TO THE FRONT OF MIGRATING ENDOTHELIAL-CELLS AT THE EDGE OF AN IN-VITRO WOUND

Citation
Ds. Ettenson et Ai. Gotlieb, BASIC FIBROBLAST GROWTH-FACTOR IS A SIGNAL FOR THE INITIATION OF CENTROSOME REDISTRIBUTION TO THE FRONT OF MIGRATING ENDOTHELIAL-CELLS AT THE EDGE OF AN IN-VITRO WOUND, Arteriosclerosis, thrombosis, and vascular biology, 15(4), 1995, pp. 515-521
Citations number
37
Categorie Soggetti
Cardiac & Cardiovascular System","Peripheal Vascular Diseas
ISSN journal
10795642
Volume
15
Issue
4
Year of publication
1995
Pages
515 - 521
Database
ISI
SICI code
1079-5642(1995)15:4<515:BFGIAS>2.0.ZU;2-V
Abstract
Rapid, efficient repair of the endothelium following focal endothelial wounding and denudation is regulated by a complex series of cellular processes. Directed cell migration, an early essential event in repair , is thought to be initiated by centrosome redistribution toward the f ront of the cell prior to the onset of migration. As such, centrosomal polarity may be an important regulatory event in directed endothelial cell migration. Little is known about the regulation of this process. To study this further, in vitro wounds were created down the middle o f confluent porcine aortic endothelial monolayers by mechanical denuda tion. Conditioned media collected 1 hour after wounding contained basi c fibroblast growth factor (bFGF). Antibodies directed against bFGF ad ded to the cultures at the time of wounding significantly inhibited ce ll migration and transiently inhibited centrosome redistribution. When transcription was transiently inhibited with actinomycin D, present a t 1 hour before and for 1 hour after wounding, the cells moved more sl owly (5.2+/-2.8 versus 22.7+/-5.7 mu m/h for control), taking five tim es longer for the wound to close. Throughout this period, centrosomes did not reorient to the front of the cells. When either recombinant bF GF or conditioned medium collected from control cultures at 1 hour aft er wounding was added 23 hours after actinomycin D was washed out (at which time RNA synthesis returned to control levels), the centrosomes redistributed to the front of the cells, and cells migrated at a rapid rate (17.2+/-4.2 mu m/h), similar to control. However, the recombinan t bFGF or conditioned media had no effect when added immediately after actinomycin D was removed, ie, when RNA synthesis was still inhibited . Thus, bFGF initiates centrosome redistribution by stimulating proces ses that lead to the transcription of as yet unknown essential gene(s) that are induced immediately following wounding, and this appears to be at least one mechanism by which bFGF enhances aortic endothelial mi gration and repair at the site of an endothelial wound.