Je. Anderson et al., THE TIME-COURSE OF BASIC FIBROBLAST GROWTH-FACTOR EXPRESSION IN CRUSH-INJURED SKELETAL-MUSCLES OF SJL J AND BALB/C MICE/, Experimental cell research, 216(2), 1995, pp. 325-334
Staining for basic fibroblast growth factor (bFGF), a potent mitogen,
was examined in muscle recovering from a crush injury and compared bet
ween two mouse strains with distinctly different capacities for muscle
regeneration to determine if bFGF staining and the steps and outcome
of repair were related. Immunofluorescence studies on intact and crush
ed tibialis anterior muscle were carried out at 0, 1, 3, 6, and 12 h p
ostcrush in SJL/J mice, and at 1, 2, 3, 5, 7, and 11 days after injury
in both SJL/J and BALB/c mice (n = 2 - 4). Disrupted fibers showed in
creased sarcoplasmic staining for bFGF as little as 3-6 h after injury
prior to infiltration with intensely fluorescent mononuclear cells (a
t 12-24 h). Fiber bFGF was maintained in SJL/J muscles for 2 days, but
was lower in most damaged fibers of BALB/c muscles at the same time.
Surviving stumps of crushed fibers, once sealed, exhibited sarcoplasmi
c extensions, some of which stained intensely for bFGF. These processe
s appeared to connect adjacent fiber stumps, and many were noted in as
sociation with aligned mononuclear cells (presumptive myoblasts) at th
e site of new myotube formation. In representative sections there were
more bFGF-positive mononuclear cells present in SJL/J than BALB/c mus
cles. Intense bFGF localization marked newly regenerating myotubes in
both SJL/J and BALB/c muscles, and such myotubes were more frequent an
d larger in SJL/J muscles. More bFGF was present in regenerating muscl
es of SJL/J compared with BALB/c mice (with respect to damaged myofibe
rs, mononuclear cells, and myotubes) and this correlates with the supe
rior new muscle formation seen in SJL/J mice. These studies support th
e idea of a positive relation between bFGF in damaged fibers, the bFGF
-positive mononuclear cells, and the speed and success of muscle regen
eration. (C) 1995 Academic Press, Inc.