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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Innate and adaptive immunity gene expression of human keratinocytes cultured of severe burn injury

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Alves Correa de Noronha, Silvana Aparecida [1] ; Ribeiro de Noronha, Samuel Marcos [1] ; Lanziani, Larissa Elias [1] ; Ferreira, Lydia Masako [1] ; Gragnani, Alfredo [1]
Total Authors: 5
[1] Univ Fed Sao Paulo, Div Plast Surg, Burns Treatment Unit, Univ Hosp, Sao Paulo - Brazil
Total Affiliations: 1
Document type: Journal article
Source: Acta Cirurgica Brasileira; v. 29, n. 3, p. 60-67, 2014.
Web of Science Citations: 4

PURPOSE: Evaluate the expression profile of genes related to Innate and Adaptive Immune System (IAIS) of human Primary Epidermal keratinocytes (hPEKP) of patients with severe burns. METHODS: After obtaining viable fragments of skin with and without burning, culture hKEP was initiated by the enzymatic method using Dispase (Sigma-Aldrich). These cells were treated with Trizol(R) (Life Technologies) for extraction of total RNA. This was quantified and analyzed for purity for obtaining cDNA for the analysis of gene expression using specific IAIS PCR Arrays plates (SA Biosciences). RESULTS: After the analysis of gene expression we found that 63% of these genes were differentially expressed, of which 77% were repressed and 23% were hyper-regulated. Among these, the following genes (fold increase or decrease): IL8 (41), IL6 (32), TNF (-92), HLA-E (-86), LYS (-74), CCR6 (-73), CD86 (-41) and HLA-A (-35). CONCLUSIONS: This study contributes to the understanding of the molecular mechanisms underlying wound infection caused by the burn. Furthermore, it may provide new strategies to restore normal expression of these genes and thereby change the healing process and improve clinical outcome. (AU)

FAPESP's process: 11/12945-4 - Keratinocyte growth factor, interleukin 1 beta, 6, 8, 10, 12 and tumor necrosis factor alpha in burned patients
Grantee:Alfredo Gragnani Filho
Support type: Regular Research Grants