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Methods to Evaluate Cytotoxicity and Immunosuppression of Combustible Tobacco Product Preparations
Published on: January 10, 2015
Distinct gene expression changes in human peripheral blood mononuclear cells treated with different tobacco product
Subhashini Arimilli1, Patrudu Makena2, Gang Liu2
1Eurofins Lancaster Laboratories PSS, Winston-Salem, NC 27105, USA.
Abstract:
Cigarette smoking exerts diverse physiological effects including immune suppression. To better characterize the biological effects of different categories of tobacco products, a genome-wide gene expression study was performed. Transcriptomic profiling was performed in PBMCs treated with different equi-nicotine units of aqueous extracts of cigarette smoke (termed Whole Smoke-Conditioned Medium, or WS-CM), or a single dose smokeless tobacco extract (STE) prepared from reference tobacco products. WS-CM induced dose-dependent changes in the expression of several genes. No significant expression differences between low WS-CM and media control were detected. However, transcripts were significantly affected by medium WS-CM (479), high WS-CM (2, 703), and STE (2, 156). The overlap between medium WS-CM and STE, and high WS-CM and STE, was minimal (34 and 65 transcripts, respectively). Hierarchical clustering revealed that gene expression profiles for STE and medium WS-CM co-clustered, while those affected by the high dose of WS-CM clustered distinctly. Functional analysis revealed that WS-CM, but not STE, uniquely affected genes involved in immune cell development and inflammatory response. Cascades of upstream regulators (e.g., TNF, IL1β, NFƙB) were identified for the observed gene expression changes and generally suppressed by WS-CM, but not by STE. Collectively, these findings demonstrate that combustible and non-combustible tobacco products elicit distinct biological effects, which could explain the observed chronic immune suppression in smokers.
Insights
Cigarette smoke and smokeless tobacco have distinct effects on gene expression and immune responses. Whole smoke-conditioned medium (WS-CM) uniquely impacts immune cell development and inflammation, unlike smokeless tobacco extract (STE).
Area of Science:
- Immunology
- Genomics
- Toxicology
Background:
- Cigarette smoking is known to cause immune suppression.
- Understanding the distinct biological effects of various tobacco products is crucial.
Purpose of the Study:
- To compare the genome-wide gene expression changes induced by cigarette smoke extract and smokeless tobacco extract.
- To elucidate the distinct biological pathways affected by different tobacco product categories.
Main Methods:
- Transcriptomic profiling of peripheral blood mononuclear cells (PBMCs).
- Treatment of PBMCs with varying doses of whole smoke-conditioned medium (WS-CM) and a single dose of smokeless tobacco extract (STE).
- Analysis of gene expression patterns, hierarchical clustering, and upstream regulator identification.
Main Results:
- Both WS-CM and STE significantly altered gene expression, with minimal overlap in affected transcripts.
- Gene expression profiles for STE and medium WS-CM co-clustered, distinct from high-dose WS-CM.
- WS-CM uniquely affected genes related to immune cell development and inflammatory response, with suppressed upstream regulators like TNF and NFκB, while STE did not.
Conclusions:
- Combustible and non-combustible tobacco products induce distinct biological effects at the genomic level.
- These differential effects may explain the chronic immune suppression observed in smokers.
- Further research into tobacco product toxicology and immunology is warranted.
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