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Chronic ethanol feeding induces subset loss and hyporesponsiveness in skin T cells.
- Source :
-
Alcoholism, clinical and experimental research [Alcohol Clin Exp Res] 2014 May; Vol. 38 (5), pp. 1356-64. Date of Electronic Publication: 2014 Feb 11. - Publication Year :
- 2014
-
Abstract
- Background: Chronic alcoholism is associated with increased incidence and severity of cutaneous infection. Skin-resident T cells orchestrate numerous immunological functions that are critically involved in both tissue homeostasis and cutaneous immunity. The impact of chronic ethanol (EtOH) exposure on skin T cells has not previously been examined; given their important role in maintaining the immune barrier function of the skin further study is warranted.<br />Methods: Mice were administered EtOH in the drinking water for 12 to 16 weeks. Flow cytometry was used to evaluate impact of EtOH feeding on skin T cell numbers, rates of proliferation, and apoptosis as well as activation marker expression and cytokine production after ex vivo stimulation.<br />Results: Chronic EtOH feeding caused a baseline reduction in dendritic epidermal T cell (DETC) numbers that corresponded with reduced expression of the activation marker JAML following phorbol 12-myristate 13-acetate (PMA)/ionomycin stimulation. Chronic EtOH feeding did not alter total numbers of dermal T cells, but specific subset loss was observed in Foxp3(+) regulatory T cells (Tregs) as well as CD3hi, Vγ3(+) and CD3int, Vγ3(-) dermal γδ T cells. EtOH-induced dysfunction in the latter population, which represents prototypical interleukin-17 (IL-17)-producing dermal γδT17s, was made evident by diminished IL-17 production following anti-CD3 stimulation. Additionally, the capacity of lymph node γδ T cells to produce IL-17 following anti-CD3 and PMA/ionomycin stimulation was impaired by chronic EtOH feeding.<br />Conclusions: Chronic EtOH feeding induced defects in both numbers and function of multiple skin T cell subsets. The decreased density and poor responsiveness of DETCs and γδT17 cells in particular would be expected to compromise immune effector mechanisms necessary to maintain a protective barrier and restrict pathogen invasion. These findings demonstrate the sensitivity of skin T cells to EtOH and provide new mechanisms to help explain the propensity of alcoholics to suffer skin infection.<br /> (Copyright © 2014 by the Research Society on Alcoholism.)
- Subjects :
- Animals
Apoptosis drug effects
Female
Flow Cytometry
Insulin-Like Growth Factor I metabolism
Interleukin-17 metabolism
Mice, Inbred C57BL
Skin cytology
Skin metabolism
T-Lymphocyte Subsets drug effects
T-Lymphocytes metabolism
Tumor Necrosis Factor-alpha metabolism
Ethanol pharmacology
Skin drug effects
T-Lymphocytes drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1530-0277
- Volume :
- 38
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Alcoholism, clinical and experimental research
- Publication Type :
- Academic Journal
- Accession number :
- 24512045
- Full Text :
- https://doi.org/10.1111/acer.12358