Genetic analysis of skin wound healing and scarring in a porcine model

被引:42
作者
Gallant-Behm, CL
Hart, DA
机构
[1] Univ Calgary, McCaig Ctr Joint Injury & Arthrit Res, Dept Microbiol & Infect Dis, Fac Med, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Fac Med, Dept Surg, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Fac Med, Dept Med, Calgary, AB T2N 4N1, Canada
关键词
D O I
10.1111/j.1524-475X.2005.00087.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Contraction is a normal part of skin wound healing and wound closure; however, excessive contraction and severe scarring concern patients and physicians alike. The present study has investigated the degree and kinetics of wound contraction in a porcine model of wound healing, to elucidate the genetic and molecular basis for abnormal skin wound healing and scarring. Healing of excisional skin wounds in juvenile female Yorkshire pigs closely resembled normal healing in humans. In contrast, identical wounds in female red Duroc pigs contracted significantly more, forming hypercontracted, hyperpigmented scars. Yorkshire x red Duroc F1 animals healed without hyperpigmentation, but with significantly greater wound contraction than observed in either parent breed. To examine the genetic transmission of the hypercontractile phenotype, all F1 animals were bred to a single Yorkshire boar, generating 20 backcross animals. All backcross animals healed with significantly less contraction than the normal Yorkshire animals. These findings suggest that the genetic contribution to scar phenotype in this animal model is complex, with a limited number of major genes controlling wound contraction, and an unknown number of minor genes that appear to modulate the impact of the major genes.
引用
收藏
页码:46 / 54
页数:9
相关论文
共 31 条
[1]  
Brissett A E, 2001, Facial Plast Surg, V17, P263, DOI 10.1055/s-2001-18827
[2]   Wound size and gestational age modulate scar formation in fetal wound repair [J].
Cass, DL ;
Bullard, KM ;
Sylvester, KG ;
Yang, EY ;
Longaker, MT ;
Adzick, NS .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (03) :411-415
[3]   Vanadate and the absence of myofibroblasts in wound contraction [J].
Ehrlich, HP ;
Keefer, KA ;
Myers, RL ;
Passaniti, A .
ARCHIVES OF SURGERY, 1999, 134 (05) :494-501
[4]   TGF-β1-mediated fibroblast-myofibroblast terminal differentiation -: the role of Smad proteins [J].
Evans, RA ;
Tian, YC ;
Steadman, R ;
Phillips, AO .
EXPERIMENTAL CELL RESEARCH, 2003, 282 (02) :90-100
[5]   Molecular, histologic, and gross phenotype of skin wound healing in red Duroc pigs reveals an abnormal healing phenotype of hypercontracted, hyperpigmented scarring [J].
Gallant, CL ;
Olson, ME ;
Hart, DA .
WOUND REPAIR AND REGENERATION, 2004, 12 (03) :305-319
[6]  
GALLANTBEHM CL, IN PRESS BURNS
[7]  
GALLANTBEHM CL, 2005, IN PRESS J CUTAN MED
[8]   Cell biology of gingival wound healing [J].
Häkkinen, L ;
Uitto, VJ ;
Larjava, H .
PERIODONTOLOGY 2000, 2000, 24 :127-152
[9]   Recombinant human platelet-derived growth factor and transforming growth factor-β mediated contraction of human dermal fibroblast populated lattices is inhibited by Rho/GTPase inhibitor but does not require phosphatidylinositol-3′ kinase [J].
Han, YP ;
Nien, YD ;
Garner, WL .
WOUND REPAIR AND REGENERATION, 2002, 10 (03) :169-176
[10]   Apoptosis of hair follicle cells in the second-degree burn wound under hypernatremic conditions [J].
Harada, T ;
Izaki, S ;
Tsutsumi, H ;
Kobayashi, M ;
Kitamura, K .
BURNS, 1998, 24 (05) :464-469