Dataset Information

Response of human skin to esthetic scarification.

ABSTRACT: This study was undertaken to investigate changes in RNA expression in previously healthy adult human skin following thermal injury induced by contact with hot metal that was undertaken as part of esthetic scarification, a body modification practice. Subjects were recruited to have pre-injury skin and serial wound biopsies performed. 4 mm punch biopsies were taken prior to branding and 1 h, 1 week, and 1, 2 and 3 months after injury. RNA was extracted and quality assured prior to the use of a whole-genome based bead array platform to describe expression changes in the samples using the pre-injury skin as a comparator. Analysis of the array data was performed using k-means clustering and a hypergeometric probability distribution without replacement and corrections for multiple comparisons were done. Confirmatory q-PCR was performed. Using a k of 10, several clusters of genes were shown to co-cluster together based on Gene Ontology classification with probabilities unlikely to occur by chance alone. OF particular interest were clusters relating to cell cycle, proteinaceous extracellular matrix and keratinization. Given the consistent expression changes at 1 week following injury in the cell cycle cluster, there is an opportunity to intervene early following burn injury to influence scar development.

SUBMITTER: Gabriel VA

PROVIDER: S-EPMC4336194 | biostudies-literature | 2014 Nov

REPOSITORIES: biostudies-literature

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Response of human skin to esthetic scarification.

Gabriel Vincent A VA McClellan Elizabeth A EA Scheuermann Richard H RH

Burns : journal of the International Society for Burn Injuries 20140228 7

This study was undertaken to investigate changes in RNA expression in previously healthy adult human skin following thermal injury induced by contact with hot metal that was undertaken as part of esthetic scarification, a body modification practice. Subjects were recruited to have pre-injury skin and serial wound biopsies performed. 4 mm punch biopsies were taken prior to branding and 1 h, 1 week, and 1, 2 and 3 months after injury. RNA was extracted and quality assured prior to the use of a who ...[more]

PMID: 24582755

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Project description:To study the effects of scarification on gene expression in the skin we performed microarray analysis on intact skin (control) and skin collected 2 h after scarification. Comparison of microarray data between the two groups showed that 451 probe sets (1.0% of a total 45038 probe sets on the arrays) representing 338 known genes were upregulated ≥ 2.0 fold in scarified skin samples when compared to controls. Further analyses of these genes showed that many were associated with an inflammatory immune response. Others were associated with wound-repair, response to stress, apoptosis and transcriptional regulation. The induction of high levels of genes encoding the neutrophil chemoattractants Cxcl1 and Cxcl2, the G-CSF receptor Csf3r, the GM-CSF receptor Csf2rb, the calcium binding proteins S100a8 and a9 (S100a8 and S100a9, respectively) the cytokines Ilb and Il6, and Cd14, Mmp9 and Sell, amongst many others, suggested a significant influx of neutrophillic granulocytes into the skin after scarification. Indeed, the expression of Cxcl2 and Il1b were up-regulated 50 fold in scarified skin when compared to intact skin. C57BL/6 mice (6-12 weeks old), 2-3 per group used. Prior to scarification approximately 1 cm2 area of hair covering the site of scarification was trimmed using curved scissors and then removed completely with an electric razor. Twenty-four hours later a 23-gauge needle was used to create a 5 mm long abrasion in the epidermal layers of the skin at the scarification site. 2 h later, ear skin was collected into RNAlater (Ambion, location) and stored at -80 oC prior to analysis. The quality of RNA for microarray analysis was first determined on an Agilent BioAnalyzer 2100 (Agilent Technologies). RNA was reverse transcribed to cDNA, amplified and labelled using the Genechip 3’ IVT Express Labelling Kit (Affymetrix, Santa Clara, CA, USA) according to the manufacturer’s instructions. Samples were hybridized to HT_MG-430_PM Affymetrix chips (Affymetrix), stained and scanned by ARK Genomics (ARK Genomics, Edinburgh, UK).

Dataset Information

Response of human skin to esthetic scarification.

Publications

Response of human skin to esthetic scarification.

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