Alcohol
Volume 21, Issue 1 , Pages 87-95, May 2000

Mechanisms of suppression of poly I:C-induced activation of NK cells by ethanol

  • Stephanie D Collier

      Affiliations

    • Current address: USDA Poultry Lab, USDA-REE-ARS-MSA-PR, 810 Hwy 12 West, Mississippi State, MS 39762, USA.
  • ,
  • Stephen B Pruett

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: 318-675-4386; fax: 318-675-5889

Department of Cellular Biology and Anatomy, Louisiana State University Health Sciences Center, 1501 Kings Highway, Sheveport, LA 71130, USA

Received 10 January 2000; received in revised form 28 February 2000; accepted 6 March 2000.

Abstract 

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-α (IFN-α) is involved and if this is associated with inhibited upregulation of perforin or granzyme B. Treatment of mice with poly I:C upregulated IFN-α and granzyme B, but not perforin, in the spleen. Administration of EtOH before poly I:C prevented the upregulation of IFN-α and granzyme B and decreased perforin levels. EtOH exposure in vivo rendered splenocytes less able to respond to IFN-α upon in vitro exposure to poly I:C. Exogenous IFN-α only partially prevented this decreased response. Thus, decreased production of and response to IFN-α 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.

Keywords:  Natural killer cells, Ethanol, Poly I:C, Interferon-α, Perforin, Granzyme B

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0741-8329(00)00087-2

Alcohol
Volume 21, Issue 1 , Pages 87-95, May 2000