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Journal ArticleDOI

Time course of the angiogenic response during normotrophic and hypertrophic scar formation in humans.

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TLDR
The differential expression of angiogenic factors in time is associated with an increased vascular density in HSs compared with normotrophic scars, and urokinase‐type plasminogen activator in time was up‐regulated during HS formation.
Abstract
Previous research suggests that in hypertrophic scars (HSs), an excess of microvessels is present compared with normotrophic scars (NSs). The aim of our study was to quantify vascular densities in HSs and normotrophic scars and to provide an insight into the kinetics of changes in the expression of angiogenic factors in time during wound healing and HS formation. Human presternal wound healing after cardiothoracic surgery through a sternotomy incision was investigated in a standardized manner. Skin biopsies were collected at consecutive time points, i.e., during surgery and 2, 4, 6, 12, and 52 weeks postoperatively. The expression levels of angiopoietin-1, angiopoietin-2, Tie-2, vascular endothelial growth factor, and urokinase-type plasminogen activator were measured by real-time reverse transcription-polymerase chain reaction. Quantification of angiogenesis and cellular localization of the proteins of interest were based on immunohistochemical analysis. Microvessel densities were higher in the HSs compared with the normotrophic scars 12 weeks (p=0.017) and 52 weeks (p=0.030) postoperatively. Angiopoietin-1 expression was lower in the hypertrophic group (p<0.001), which, together with a nonsignificant increase of angiopoietin-2 expression, represented a considerable decrease in the angiopoietin-1/angiopoietin-2 ratio in the hypertrophic group 4 weeks (p=0.053), 12 weeks (p<0.001), and 52 weeks (p<0.001) postoperatively. The expression of urokinase-type plasminogen activator was up-regulated during HS formation (p=0.008). Vascular endothelial growth factor expression was not significantly different when comparing both groups. In summary, the differential expression of angiopoietin-1, angiopoietin-2, and urokinase-type plasminogen activator in time is associated with an increased vascular density in HSs compared with normotrophic scars.

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Citations
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The role of the TGF-β family in wound healing, burns and scarring: a review.

TL;DR: The role of growth factor TGF-β in the process of wound healing and scar formation has been investigated in this paper, showing that TGFβ1 was responsible for the fibrotic scarring response whereas the scarless wound healing seen in fetal wounds was due to increased levels of TGF β3.
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Angiogenesis and wound repair: when enough is enough

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Detrimental dermal wound healing: what can we learn from the oral mucosa?

TL;DR: Oral wounds contained fewer immune mediators, blood vessels, and profibrotic mediators but had more bone marrow–derived cells, a higher reepithelialization rate, and faster proliferation of fibroblasts compared with dermal wounds, forming a basis for further research on the relations among ECM, immune cells, growth factors, and fibroblast phenotypes.
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Tissue Engineering and Regenerative Repair in Wound Healing

TL;DR: The elements that distinguish fetal scarless and adult scarring wound healing are described, current trends in tissue engineering aimed at achieving scarless tissue regeneration are discussed, and recent advances in biomaterials and stem cell applications are discussed.
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Apoptosis and angiogenesis: an evolving mechanism for fibrosis

TL;DR: This review specifically examines the correlation between the presence of apoptotic cells and their effect on fibroblast phenotype and collagen metabolism in several different experimental models of fibrosis, suggesting that the vascular apoptotic burden may be important to fibrotic outcomes.
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Angiogenesis in Wound Healing

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