Cytokine and growth factor mRNA expression patterns associated with the hypercontracted, hyperpigmented healing phenotype of red duroc pigs: A model of abnormal human scar development?

被引:32
作者
Gallant-Behm, Corrie L.
Olson, Merle E.
Hart, David A. [1 ]
机构
[1] Univ Calgary, Fac Med, Dept Surg, Calgary, AB, Canada
[2] Univ Calgary, Fac Med, Dept Med, Calgary, AB, Canada
[3] Univ Calgary, Fac Med, Dept Microbiol & Infect Dis, Calgary, AB, Canada
[4] Univ Calgary, Fac Sci, Dept Biol Sci, Calgary, AB, Canada
[5] Univ Calgary, McCaig Ctr Joint Injury & Arthrit Res, Calgary, AB T2N 4N1, Canada
关键词
D O I
10.1007/s10227-005-0105-4
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Background: Skin wounds in red Duroc pigs heal with the formation of hypercontractile, hyperpigmented scars, similar in some respects to human hypertrophic scars. Objective The goal of this study was to characterize the mRNA expression patterns for a subset of relevant cytokines, growth factors, receptors, and transcriptiou factors involved in the red Duroc scarring phenotype. Methods: Full-thickness and deep dermal wounds were created on the backs of juvenile female red Duroc pigs. Samples were taken every two weeks postwounding and total RNA and DNA were extracted and quantified. RT-PCR was performed using porcine gene-specific primers for 15 relevant molecules. Results: The majority of molecules examined exhibited a biphasic pattern of expression, with peaks of expression at days 14 and 56 postinjury. Conclusions. The molecular expression pattern observed correlates well with the gross healing phenotype and matrix molecule expression patterns previously reported in red Duroc pigs. These findings enhance our understanding of the processes associated with fibroproliferative scar-formation.
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页码:165 / 177
页数:13
相关论文
共 65 条
[1]
COLLAGENASE IN WOUND-HEALING - EFFECT OF WOUND AGE AND TYPE [J].
AGREN, MS ;
TAPLIN, CJ ;
WOESSNER, JF ;
EAGLSTEIN, WH ;
MERTZ, PM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (06) :709-714
[2]
GELATINASE ACTIVITY DURING WOUND-HEALING [J].
AGREN, MS .
BRITISH JOURNAL OF DERMATOLOGY, 1994, 131 (05) :634-640
[3]
Akimoto S, 1999, EUR J DERMATOL, V9, P357
[4]
Bailly S, 1996, EUR CYTOKINE NETW, V7, P125
[5]
The effect of TGF-beta on keloid fibroblast proliferation and collagen synthesis [J].
Bettinger, DA ;
Yager, DR ;
Diegelmann, RF ;
Cohen, IK .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1996, 98 (05) :827-833
[6]
Altered levels of extracellular matrix molecule mRNA in healing rabbit ligaments [J].
Boykiw, R ;
Sciore, P ;
Reno, C ;
Marchuk, L ;
Frank, CB ;
Hart, DA .
MATRIX BIOLOGY, 1998, 17 (05) :371-378
[7]
Nrf2 transcription factor, a novel target of keratinocyte growth factor action which regulates gene expression and inflammation in the healing skin wound [J].
Braun, S ;
Hanselmann, C ;
Gassmann, MG ;
Keller, UAD ;
Born-Berclaz, C ;
Chan, KM ;
Kan, YW ;
Werner, S .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (15) :5492-5505
[8]
Growth factors in the repair of partial thickness porcine skin wounds [J].
Breuing, K ;
Andree, C ;
Helo, G ;
Slama, J ;
Liu, PY ;
Eriksson, E .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1997, 100 (03) :657-664
[9]
Chou DHI, 1996, J IMMUNOL, V156, P4354
[10]
Mediation of transforming growth factor-β1-stimulated matrix contraction by fibroblasts -: A role for connective tissue growth factor in contractile scarring [J].
Daniels, JT ;
Schultz, GS ;
Blalock, TD ;
Garrett, Q ;
Grotendorst, GR ;
Dean, NM ;
Khaw, PT .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (05) :2043-2052