Please use this identifier to cite or link to this item: https://doi.org/10.1007/7651_2018_163
Title: Full-thickness human skin equivalent models of atopic dermatitis
Authors: Sriram, G 
Bigliardi, PL 
Bigliardi-Qi, M
Keywords: 3D tissue constructs
Atopic dermatitis
Fibrin
Full-thickness
Human skin equivalent
Organoids
Organotypic culture
Tissue engineering
Cells, Cultured
Cytokines
Dermatitis, Atopic
Fibrin
Fibroblasts
Humans
Keratinocytes
Models, Biological
Skin
Skin, Artificial
Tissue Engineering
Issue Date: 1-Jan-2019
Publisher: Springer New York
Citation: Sriram, G, Bigliardi, PL, Bigliardi-Qi, M (2019-01-01). Full-thickness human skin equivalent models of atopic dermatitis. Methods in Molecular Biology 1879 : 367-383. ScholarBank@NUS Repository. https://doi.org/10.1007/7651_2018_163
Abstract: Atopic dermatitis is a chronic inflammatory skin disease caused by complex multifactorial etiology. In the recent years, there have been significant advances in tissue engineering and the generation of in vitro skin models representative of healthy and diseased states. This chapter describes the methodology for the fabrication of in vitro human skin equivalent (HSE) from human keratinocytes and fibroblasts using a fibrin-based dermal matrix and serum-free culture conditions. Modification of the culture conditions with the supplementation of Th2 cytokines such as interleukin-4 induces the development of atopic dermatitis-like skin model. The chapter also describes the histological and immunohistochemical tools for characterization of the HSE model. The reconstruction of tissue-engineered HSE models that recapitulate the essential features of atopic dermatitis provides powerful tools for deeper understanding of the underlying pathological mechanisms on epidermal level, identification and testing of novel treatment options, and safety and toxicological evaluation in a pathophysiologically relevant system.
Source Title: Methods in Molecular Biology
URI: https://scholarbank.nus.edu.sg/handle/10635/247531
ISBN: 9781493988693
DOI: 10.1007/7651_2018_163
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