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
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
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.