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TNF-alpha Expression Patterns as Potential Molecular Biomarker for Human Skin Cells Exposed to Vesicant Chemical Warfare Agents: Sulfur Mustard (HD) and Lewisite (L)

机译:TNF-α表达模式作为人类皮肤细胞的潜在分子生物标志物暴露于Vesicant化学战剂:硫芥子(HD)和Lewisite(L)

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Studies were conducted to examine the effect of two vesicant chemical warfare agents (VCWA), one of them an arsenical, on cytokine gene expression in normal human epidermal keratinocyte (NHEK) cells. We tested 2, 2's -dichlorethylsulfide (sulfur mustard, military designation HD) and 2, chlorovinyldichloroarsine (Lewisite, military designation L), which have significant differences in their chemical, physical, and toxicological properties. Human tumor necrosis factor-alpha (hTNF-alpha cytokine) was detected by using the enzyme-linked immunosorbent assay, a protein multiplex immunoassay, Luminex100(Trade mark), and reverse transcription-polymerase chain reaction (RT- PCR). The messenger RNA expression of hTNF-alpha was determined to provide a semi-quantitative analysis. HD-stimulated NHEK induced secretion of hTNF-alpha in a dose-dependent manner. Dose response effect of Lewisite decreased hTNF- alpha levels. Time-response data indicated that the maximum response for HD occurred at 24 h with an associated cytotoxic concentration of 10(exp -4) mol/L. NHEK cells stimulated with 10(exp -4) mol/ LHD for 24 h at 37 degrees C increased detectable levels of hTNF-alpha from 5 to 28 ng/ml at an index of cell viability between 85 to 93% as detected by Luminex100(Trade Mark). Our results indicated that the increased levels of hTNF-alpha by HD are dependent on the primary cultures, cell densities, and chemical properties of the stimulation. Lewisite under the same conditions as HD caused a reduction of hTNF-alpha from control levels of 1.5 ng/ml to 0.3 ng/ml after stimulation (10 (exp -4) mol/L), with an index of cell viability of approximately 34%. We analyzed the transcriptional of hTNF-alpha gene and found that HD (10(exp -6) to 10(exp -4) mol/L) activates the hTNF-alpha gene in cultured NHEK and that L at 10(exp 6) to 10(exp -4) mol/L markedly reduces the hTNF-alpha gene.

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