Abstract

Skin aging shows an imbalance between synthesis and degradation of the extracellular matrix. The overproduction of degradative enzymes (MMPs) during the chronology- and photo-induced aging leads to a degradation of the elastic and collagen networks. In a model of collagen and elastin destruction, we showed that the gingival fibroblast was able to preserve these macromolecules by inhibiting the overproduction of metalloproteinases by overproduction of TIMP-1 and modulation of the inflammatory cytokines activity. The objective of this study is to evaluate the effect of the gingival fibroblasts on human skin. The results in vitro and ex vivo show that the gingival fibroblast protects the skin collagen and elastic network by the inhibition of MMPs which leads to an overproduction of the TIMP-1. Moreover, the gingival fibroblast modulates the activity of some enzymes responsible for the inflammation; they inhibit the IL-1β and stimulate the production of TGF-β1. In vivo studies with a duration of six months and 50 women with pronounced wrinkles show that the culture supernatant of gingival fibroblasts diluted to 5% leads to a statistically significant decrease in the number and length of wrinkles.

Highlights

  • In skin ageing, a disequilibrium occurs in the balance between the synthesis of the extracellular matrix (ECM) and its degradation by matrix metalloproteases (MMPs)

  • The human gingival fibroblast (hGF) in coculture with irradiated skin causes a decrease of the amount of MMP-1 (-1.7 fold), MMP-3 (-1.5 fold) and MMP-9 (-2.2 fold)

  • There is a smaller decrease in coculture with the presence of Human dermal fibroblast (hDF): -1.2 times respectively for MMP-1 and MMP-3 and -1.3 times for MMP-9

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Summary

Introduction

A disequilibrium occurs in the balance between the synthesis of the extracellular matrix (ECM) and its degradation by matrix metalloproteases (MMPs). This disequilibrium leads to an excessive degradation of the extracellular matrix, a characteristic of skin ageing [1]. Skin ageing is associated to an increase of the number and the deepness of wrinkles, a direct consequence of the degradation of macromolecules of the dermis, such as collagens and elastin. Collagenases-1 (MMP-1) degrade collagens, while gelatinases A and B (MMP-2 and MMP-9) degrade elastin. It is evident that the activity of the MMPs is one of the keys of the skin ageing and that these enzymes have to be the target of therapeutic activities [3,4]

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