Regenerative potential of adipocytes in hypertrophic scars is mediated by myofibroblast reprogramming

Item Type:	Article
Title:	Regenerative potential of adipocytes in hypertrophic scars is mediated by myofibroblast reprogramming
Creators Name:	Hoerst, K. and van den Broek, L. and Sachse, C. and Klein, O. and von Fritschen, U. and Gibbs, S. and Hedtrich, S.
Abstract:	Abnormal scarring is a major challenge in modern medicine. The central role of myofibroblasts and TGF-β signaling in scarring is widely accepted, but effective treatment options are missing. Autologous fat grafting is a novel approach that has led to significant improvements in the functionality and appearance of scar tissue. While the underlying mechanism is unknown, the potential role of paracrine effects of adipocytes has been discussed. Hence, with the aim of unraveling the regenerative potential of adipocytes, their effects on in vitro differentiated myofibroblasts and on fibroblasts from hypertrophic scars were investigated. Exposure to adipocyte-conditioned medium significantly decreased the expression of the myofibroblast marker α-SMA and ECM components, indicating the occurrence of myofibroblast reprogramming. Further analysis demonstrated that myofibroblast reprogramming was triggered by BMP-4 and activation of PPARγ signaling initiating tissue remodeling. These findings may pave the way for novel therapeutic strategies for the prevention or treatment of hypertrophic scars. KEY MESSAGES: Adipocytes induce distinct regenerative effects in hypertrophic scar tissue. Adipocytes secrete several proteins which are involved in wound healing and regeneration. Adipocytes secrete BMP-4 which activates myofibroblast reprogramming. Mediators secreted by adipocytes directly and indirectly activate PPARγ which exerts distinct anti-fibrotic effects. These findings may pave the way for novel therapeutic strategies for the prevention or treatment of hypertrophic scars.
Keywords:	Myofibroblast, Wound Healing, Hypertrophic Scar, Adipocyte, Bone Morphogenetic Protein
Source:	Journal of Molecular Medicine
ISSN:	0946-2716
Publisher:	Springer
Volume:	97
Number:	6
Page Range:	761-775
Date:	1 June 2019
Official Publication:	https://doi.org/10.1007/s00109-019-01772-2
PubMed:	View item in PubMed

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