2011
DOI: 10.1111/j.1742-481x.2011.00771.x
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The evidence for the role of transforming growth factor‐beta in the formation of abnormal scarring

Abstract: The complex biological and physiological mechanisms that result in poor quality scarring are still not fully understood. This review looks at current evidence of the role of transforming growth factor-beta (TGFβ) in this pathological process.

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Cited by 54 publications
(38 citation statements)
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“…The increase or prolonged activity of TGF-b1 leads to an overproduction and excess deposition of collagen by fibroblasts that often result in hypertrophic scars. 128 In an adult rat incisional model, the addition of neutralizing antibody to reduce levels of TGFb1 and TGFb2 resulted in reduced collagen content, improved orientation of ECM in the wound, and less scarring compared with controls. 129 …”
Section: Transforming Growth Factor-bmentioning
confidence: 97%
“…The increase or prolonged activity of TGF-b1 leads to an overproduction and excess deposition of collagen by fibroblasts that often result in hypertrophic scars. 128 In an adult rat incisional model, the addition of neutralizing antibody to reduce levels of TGFb1 and TGFb2 resulted in reduced collagen content, improved orientation of ECM in the wound, and less scarring compared with controls. 129 …”
Section: Transforming Growth Factor-bmentioning
confidence: 97%
“…Subsequently, the dermis formed in the 45 presence of the PHBV loaded with ASCs possesses a more complex collagen structure. Additionally, an 46 anti-scarring effect was observed in the presence of the PHBV scaffold indicated by a down-regulation 47 of TGF-b1 and a-SMA together with an increase of TGF-b3, when associated with ASCs. These results indi- 48 cate that although PHBV scaffold was able to guide the wound healing process with reduced scarring, the 49 presence of ASCs was crucial to enhance vascularization and provide a better quality neo-skin.…”
mentioning
confidence: 93%
“…Great attention has been 513 brought to the secretion of those cytokines during wound healing 514 since a direct correlation with scar formation has been confirmed 515[45]. Overexpression of TGF-b1 results in excessive fibroblast 516 migration and myofibroblast differentiation, and therefore on the 517 deposition of a highly organized ECM over-accumulation and scar 518 formation[46,47]. On the other side, TGF-b3 inhibits scarring by519 promoting normal collagen organization[41,48].…”
mentioning
confidence: 99%
“…Moreover, after fibroblasts differentiate into myofibroblasts, they also start to express α-SMA and acquire a contractile phenotype that promotes wound closure [34]. The lower expression of TGF-β1 resulted in less myofibroblast differentiation, as indicated by the lower expression of α-SMA in the GF + MSCs group (Fig.…”
Section: Accepted Manuscriptmentioning
confidence: 90%
“…6). TGF-β1 promotes fibroblast migration, myofibroblast differentiation, and followed ECM over-accumulation and scar formation [33,34]. On the contrary, TGF-β3 inhibits scar formation by promoting normal collagen organization [30,35].…”
Section: Accepted Manuscriptmentioning
confidence: 99%