期刊
ALCOHOL
卷 21, 期 1, 页码 87-95出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/S0741-8329(00)00087-2
关键词
natural killer cells; ethanol; poly I : C; interferon-alpha; perforin; granzyme B
资金
- NIAAA NIH HHS [AA09505] Funding Source: Medline
We have previously reported that ethanol (EtOH) decreases polyinosinic- polycytidylic acid (poly I:C) and interleukin-2 (IL-2)-induced upregulation of natural killer (NK) cell lytic activity in mice. The present study was designed to determine if decreased production of or response to interferon-alpha (IFN-alpha) is involved and if this is associated with inhibited upregulation of perforin or granzyme B. Treatment of mice with poly I:C upregulated IFN-alpha and granzyme B, but not perforin, in the spleen. Administration of EtOH before poly I:C prevented the upregulation of IFN-alpha and granzyme B and decreased perforin levels. EtOH exposure in vivo rendered splenocytes less able to respond to IFN-alpha upon in vitro exposure to poly I:C. Exogenous IFN-alpha only partially prevented this decreased response. Thus, decreased production of and response to IFN-alpha as well as decreased levels of granzyme B and perforin are implicated in the diminished activation of NK cell lytic function in EtOH-treated mice. (C) 2000 Elsevier Science Inc. All rights reserved.
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