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Critical Role of Transforming Growth Factor Beta in Different Phases of Wound Healing

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Date 2014 Feb 15
PMID 24527344
Citations 202
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Abstract

Significance: This review highlights the critical role of transforming growth factor beta (TGF-β)1-3 within different phases of wound healing, in particular, late-stage wound healing. It is also very important to identify the TGF-β1-controlling factors involved in slowing down the healing process upon wound epithelialization.

Recent Advances: TGF-β1, as a growth factor, is a known proponent of dermal fibrosis. Several strategies to modulate or regulate TGF's actions have been thoroughly investigated in an effort to create successful therapies. This study reviews current discourse regarding the many roles of TGF-β1 in wound healing by modulating infiltrated immune cells and the extracellular matrix.

Critical Issues: It is well established that TGF-β1 functions as a wound-healing promoting factor, and thereby if in excess it may lead to overhealing outcomes, such as hypertrophic scarring and keloid. Thus, the regulation of TGF-β1 in the later stages of the healing process remains as critical issue of which to better understand.

Future Directions: One hypothesis is that cell communication is the key to regulate later stages of wound healing. To elucidate the role of keratinocyte/fibroblast cross talk in controlling the later stages of wound healing we need to: (1) identify those keratinocyte-released factors which would function as wound-healing stop signals, (2) evaluate the functionality of these factors in controlling the outcome of the healing process, and (3) formulate topical vehicles for these antifibrogenic factors to improve or even prevent the development of hypertrophic scarring and keloids as a result of deep trauma, burn injuries, and any type of surgical incision.

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References
1.
Waddington S, Crossley R, Sheard V, Howe S, Buckley S, Coughlan L . Gene delivery of a mutant TGFβ3 reduces markers of scar tissue formation after cutaneous wounding. Mol Ther. 2010; 18(12):2104-11. PMC: 2997585. DOI: 10.1038/mt.2010.174. View

2.
Shirakata Y, Kimura R, Nanba D, Iwamoto R, Tokumaru S, Morimoto C . Heparin-binding EGF-like growth factor accelerates keratinocyte migration and skin wound healing. J Cell Sci. 2005; 118(Pt 11):2363-70. DOI: 10.1242/jcs.02346. View

3.
Thompson H, Mih J, Krasieva T, Tromberg B, George S . Epithelial-derived TGF-beta2 modulates basal and wound-healing subepithelial matrix homeostasis. Am J Physiol Lung Cell Mol Physiol. 2006; 291(6):L1277-85. DOI: 10.1152/ajplung.00057.2006. View

4.
KATZ A, Taichman L . A partial catalog of proteins secreted by epidermal keratinocytes in culture. J Invest Dermatol. 1999; 112(5):818-21. DOI: 10.1046/j.1523-1747.1999.00572.x. View

5.
Kilani R, Guilbert L, Lin X, Ghahary A . Keratinocyte conditioned medium abrogates the modulatory effects of IGF-1 and TGF-beta1 on collagenase expression in dermal fibroblasts. Wound Repair Regen. 2007; 15(2):236-44. DOI: 10.1111/j.1524-475X.2007.00210.x. View