TGF-β:: A fibrotic factor in wound scarring and a potential target for anti-scarring gene therapy

被引:97
作者
Liu, W [1 ]
Wang, DR [1 ]
Cao, YL [1 ]
机构
[1] Shanghai Med Univ 2, Shanghai 9th Peoples Hosp, Dept Plast & Reconstruct Surg, Shanghai Inst Plast & Reconstruct Surg, Shanghai 200011, Peoples R China
关键词
wound scarring; TGF-beta; gene therapy; adenovirus; gene transfer;
D O I
10.2174/1566523044578004
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Hypertrophic scar and keloid are common and difficult to treat diseases in plastic surgery. Results of wound healing research over the past decades have demonstrated that transforming growth factor-beta (TGF-beta) plays an essential role in cutaneous scar formation. In contrast, fetal wounds, which heal without scarring, contain a lower level of TGF-beta than adult wounds. How to translate the discovery of basic scientific research into the clinical treatment of wound scarring has become an important issue to both clinicians and basic researchers. The development of gene therapy techniques offers the potential to genetically modify adult wound healing to a healing process similar to fetal wounds, and thus reduces wound scarring. This article intends to review the roles of TGF-beta in the formation of wound scarring, the possible strategies of antagonizing wound TGF-beta, and our preliminary results of scar gene therapy, which show that wound scarring can be significantly reduced by targeting wound TGF-beta.
引用
收藏
页码:123 / 136
页数:14
相关论文
共 112 条
[1]
Decorin suppresses transforming growth factor-β-induced expression of plasminogen activator inhibitor-1 in human mesangial cells through a mechanism that involves Ca2+-dependent phosphorylation of Smad2 at serine-240 [J].
Abdel-Wahab, N ;
Wicks, SJ ;
Mason, RM ;
Chantry, A .
BIOCHEMICAL JOURNAL, 2002, 362 (03) :643-649
[2]
A new experimental hypertrophic scar model in guinea pigs [J].
Aksoy, HM ;
Vargel, I ;
Canter, HI ;
Erk, Y ;
Sargon, M ;
Pinar, A ;
Tezel, GG .
AESTHETIC PLASTIC SURGERY, 2002, 26 (05) :388-396
[3]
MEMBRANE-ANCHORED AND SOLUBLE FORMS OF BETAGLYCAN, A POLYMORPHIC PROTEOGLYCAN THAT BINDS TRANSFORMING GROWTH FACTOR-BETA [J].
ANDRES, JL ;
STANLEY, K ;
CHEIFETZ, S ;
MASSAGUE, J .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :3137-3145
[4]
Mice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response [J].
Ashcroft, GS ;
Yang, X ;
Glick, AB ;
Weinstein, M ;
Letterio, JJ ;
Mizel, DE ;
Anzano, M ;
Greenwell-Wild, T ;
Wahl, SM ;
Deng, CX ;
Roberts, AB .
NATURE CELL BIOLOGY, 1999, 1 (05) :260-266
[5]
KELOID FIBROBLASTS EXHIBIT AN ALTERED RESPONSE TO TGF-BETA [J].
BABU, M ;
DIEGELMANN, R ;
OLIVER, N .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (05) :650-655
[6]
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
[7]
NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364
[8]
Physicochemical Activation of Recombinant Latent Transforming Growth Factor-beta's 1, 2, and 3 [J].
Brownh, Peter D. ;
Wakefiel, Lalage M. ;
Levinson, Arthur D. ;
Sporn, Michael B. .
GROWTH FACTORS, 1990, 3 (01) :35-43
[9]
CAO HJ, 1995, INVEST OPHTH VIS SCI, V36, P1411
[10]
Stimulation of type I collagen transcription in human skin fibroblasts by TGF-β:: Involvement of Smad 3 [J].
Chen, SJ ;
Yuan, WH ;
Mori, Y ;
Levenson, A ;
Trojanowska, M ;
Varga, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (01) :49-57