L. Germain et al., HUMAN WOUND-HEALING FIBROBLASTS HAVE GREATER CONTRACTILE PROPERTIES THAN DERMAL FIBROBLASTS, The Journal of surgical research, 57(2), 1994, pp. 268-273
Contractile and phenotypic properties of human fibroblasts from healin
g wounds were compared to those of dermal fibroblasts using in vitro m
odels. Wound fibroblasts were recovered from implants, made of a polyv
inyl alcohol sponge threaded into a perforated silicone tube, 12 days
after their subcutaneous implantation in human volunteers. Dermal fibr
oblasts were isolated from the skin of healthy subjects. Two morpholog
ically different fibroblast populations were observed in cells culture
d from implants. In order to characterize these fibroblast populations
, intracellular alpha-actin expression was studied by immunofluorescen
ce labeling of cells cultured in monolayer. This protein was detected
in less than 1% of the dermal fibroblasts. By contrast, 30 to 40% of w
ound fibroblasts were labeled and contained fiber networks of alpha-ac
tin. These results confirm the presence of myofibroblasts in human wou
nd healing tissues. The contractile property of fibroblasts and myofib
roblasts was evaluated using a three-dimensional cell culture model (f
ibroblast populated collagen gels). Cells were incorporated in a colla
gen matrix and cultured for 14 days. The surface area of collagen gels
was measured every day. Our results show that wound fibroblasts stron
gly contract collagen gels during the first 24 hr (surface area at 24
hr = 20-55% of initial surface area) in comparison to dermal fibroblas
ts (surface area at 24 hr = 70-75% of initial surface area). This supe
rior level of contraction was observed until the fifth day of culture.
In conclusion, these results show that in human granulation tissue, t
he myofibroblast phenotype is abundant at Day 12 postwounding and that
granulating wound fibroblasts have greater contractile capacity than
dermal fibroblasts, in vitro. These gathered observations suggest that
myofibroblasts are responsible for wound contraction in vivo. (C) 199
4 Academic Press, Inc.