Cytokine mRNA levels and lymphocyte infiltration in pancreatic tissue during experimental chronic pancreatitis induced by dibutyltin dichloride

Dig Dis Sci. 2001 Aug;46(8):1647-56. doi: 10.1023/a:1010689117772.

Abstract

There is little information available regarding the role of inflammatory cells in the pathogenesis of chronic pancreatitis. Therefore, we analyzed the local cytokine profile and infiltrating lymphocytes in a rat model of chronic pancreatitis. Experimental pancreatitis was induced by a single intravenous application of dibultyltin dichloride (DBTC). During a time course of two months we observed the mRNA expression of cytokines using competitive RT-PCR. Lymphocytes were characterized by immunohistochemistry, FACS analysis, and the lymphocyte proliferation test. IL-1beta, IL-6, IL-5, and IL-10 were immediately up-regulated in the acute phase of disease, while lymphocyte-restricted expression of IL-2, IL-2R, and IFN-y was only found in the chronic course. Among the infiltrating lymphocytes, CD4+ cells dominated, but during the chronic process there was an increase of CD8+ cells, resulting in a reduced CD4/CD8 ratio. Mitogen-induced activation of isolated mesenteric lymph node cells increased during the chronic inflammation. Our results suggest that in experimental pancreatitis acute inflammatory reactions are followed by a T-lymphocyte-mediated process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD4-CD8 Ratio
  • Chronic Disease
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Immunohistochemistry
  • Interferon-gamma / metabolism
  • Interleukins / metabolism
  • Lymphocyte Activation
  • Lymphocytes / metabolism
  • Lymphocytes / pathology*
  • Male
  • Organotin Compounds
  • Pancreas / metabolism
  • Pancreas / pathology*
  • Pancreatitis / chemically induced
  • Pancreatitis / immunology*
  • Pancreatitis / pathology
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Lew
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocytes / physiology
  • Time Factors
  • Up-Regulation

Substances

  • Cytokines
  • Interleukins
  • Organotin Compounds
  • RNA, Messenger
  • Interferon-gamma
  • dibutyldichlorotin