Tissue-engineered human psoriatic skin supplemented with cytokines as an in vitro model to study plaque psoriasis

被引:19
|
作者
Pouliot-Berube, Claudia [1 ,2 ]
Zaniolo, Karine [3 ]
Guerin, Sylvain L. [3 ,4 ]
Pouliot, Roxane [1 ,2 ]
机构
[1] Univ Laval, Ctr Rech FRQS, Genie Tissulaire & Regenerat, Ctr LOEX,CHU Quebec,Axe Med Regeneratrice, Quebec City, PQ, Canada
[2] Univ Laval, Fac Pharm, Quebec City, PQ, Canada
[3] CHU Quebec, Ctr Rech FRQS, Ctr Univ Ophtalmol Rech, Axe Med Regeneratrice, Quebec City, PQ, Canada
[4] Univ Laval, Dept Ophthalmol, Quebec City, PQ, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
cytokines gene ontology analysis; immunology biotechnology; psoriasis transcriptome; skin gene expression profiling; tissue engineering immune response; COMBINED IMMUNODEFICIENCY MOUSE; EPIDERMOLYSIS-BULLOSA; GENE-EXPRESSION; INNATE IMMUNITY; CELL-ADHESION; ANIMAL-MODELS; T-CELL; KERATINOCYTES; TRANSCRIPTOME; FRACTALKINE;
D O I
10.2217/rme-2016-0037
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Aim: Psoriasis is a chronic inflammatory skin disease. To study its complex etiology, a psoriatic skin substitute model supplemented with a cytokine cocktail has been used. Materials & methods: Reconstructed psoriatic skin substitutes were supplemented with a cocktail of four cytokines: TNF-alpha, IL-1 alpha, IL-6 and IL-17A, to monitor their impact on gene expression by DNA microarray. Results: Gene profiling analyses identified several deregulated genes reported as being also deregulated in psoriasis skin in vivo (S100A12, IL-8, DEFB4A and KYNU). The expression of those genes was dramatically increased compared with basal levels of controls (p < 0.005 to < 0.05). Conclusion: Psoriatic substitutes supplemented with a cocktail of TNF-alpha, IL-1 alpha, IL-6 and IL-17A showed similar transcriptome alterations to those found in psoriasis.
引用
收藏
页码:545 / 557
页数:13
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