Abstract

Lack of adult cells’ ability to produce sufficient amounts of elastin and assemble functional elastic fibers is an issue for creating skin substitutes that closely match native skin properties. The effects of female sex hormones, primarily estrogen, have been studied due to the known effects on elastin post-menopause, thus have primarily included older mostly female populations. In this study, we examined the effects of female sex hormones on the synthesis of elastin by female and male human dermal fibroblasts in engineered dermal substitutes. Differences between the sexes were observed with 17β-estradiol treatment alone stimulating elastin synthesis in female substitutes but not male. TGF-β levels were significantly higher in male dermal substitutes than female dermal substitutes and the levels did not change with 17β-estradiol treatment. The male dermal substitutes had a 1.5-fold increase in cAMP concentration in the presence of 17β-estradiol compared to no hormone controls, while cAMP concentrations remained constant in the female substitutes. When cAMP was added in addition to 17β-estradiol and progesterone in the culture medium, the sex differences were eliminated, and elastin synthesis was upregulated by 2-fold in both male and female dermal substitutes. These conditions alone did not result in functionally significant amounts of elastin or complete elastic fibers. The findings presented provide insights into differences between male and female cells in response to female sex steroid hormones and the involvement of the cAMP pathway in elastin synthesis. Further explorations into the signaling pathways may identify better targets to promote elastic fiber synthesis in skin substitutes.

Highlights

  • Mature elastic fibers are a key component of the dermis that is lacking in most skin substitutes and is reduced in aging skin

  • Elastin is essential to elastic fibers; it is an insoluble protein that makes up approximately 2–4% of the human dermal extracellular matrix [1,2]

  • DTishcisusstsuidoynhas confirmed that E2 has a stimulatory effect on elastin production in engineered dermal substitutes (EDS) containing female hDF, and further shows this is via activation of the nuclear ERs, primarTilhyiEsRs-tβu. dTyhehealasstcoogennfiicrmeffeedct othf Ea2t tEre2athmaesntawsatsimabuselanttoinrymaelfefeEcDtSoanndeclAasMtiPn produ lEevDeSls cinotnhteaEinDiSngin fremspoanlesehtDo EF2, wanerde sfiugrntihfiecarnstlhyohwigshetrhiins tihsevmialeacEtDivSatthiaonninotfhtehe nucl fpemrimaleaorirlvyeEhiRcl-eβ. .TThhe eseexldaisftfoergeennceisc ienffeelacsttionfsEyn2 tthreesaistmcoeunldt wbeaeslimabinsaetnetdiwnhmenaltheeEDS an EleDvSewlserienctuhlteurEedDwSiitnh crAeMspPo, En2s,eantdo PE42

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Summary

Introduction

Mature elastic fibers are a key component of the dermis that is lacking in most skin substitutes and is reduced in aging skin. While different methods have been attempted to stimulate elastin synthesis in the skin during wound healing or to incorporate elastin into scaffolds for engineered skin substitutes, none to date have been able to form a fully functional network of mature elastic fibers. This structural omission can lead to mobility and other quality-of-life issues following treatment; a better understanding of elastin synthesis is necessary to facilitate more favorable outcomes post-injury

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