Increased expression of PI-3K in asthmatic rat T lymphocytes

J Huazhong Univ Sci Technolog Med Sci. 2007 Feb;27(1):34-6. doi: 10.1007/s11596-007-0110-5.

Abstract

In order to explore the expression of PI-3K in T lymphocytes of asthmatic rats and the relationship between PI-3K and activation of T lymphocytes, 24 Wistar rats were randomly divided into 4 groups: normal control group, asthmatic one-week group, asthmatic two-week group and asthmatic four-week group. T cells were purified from blood of each rat and the expression of PI-3K was observed by immunocytochemical fluorescence staining, the semiquantitative fluorescence intensity was measured by HPIAS-2000 analytic software, and the expression of IL-4 in supernatants was detected by ELISA. The results showed that the fluorescence intensity of T lymphocytes in asthmatic groups was significantly higher than that in normal control (P<0.001), indicating that the expression of PI-3K in T lymphocytes of asthmatic rats was significantly higher than that in those of normal controls, and the difference between acute and chronic stage asthmatic groups was significant (P<0.05). The expression levels of IL-4 protein in supernatants of asthmatic T lymphocytes were significantly higher than those in the normal controls (P<0.05). There was a significant positive correlation between the expression of PI-3K in T lymphocytes and the IL-4 protein expression in supernatants (r=0.583, P<0.01). It was suggested that PI-3K signal pathway may participate in the processes of activation and other cytological effects of asthmatic T lymphocytes, thus may play an important roles in the pathogenesis of asthma.

MeSH terms

  • Animals
  • Asthma / chemically induced
  • Asthma / immunology*
  • Asthma / metabolism
  • Asthma / pathology
  • Case-Control Studies
  • Cell Culture Techniques
  • Cells, Cultured
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique, Direct
  • Immunohistochemistry
  • Interleukin-4 / analysis
  • Interleukin-4 / genetics
  • Interleukin-4 / immunology
  • Lymphocyte Activation
  • Male
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Signal Transduction
  • T-Lymphocytes / enzymology*
  • T-Lymphocytes / immunology*
  • Time Factors

Substances

  • Interleukin-4
  • Phosphatidylinositol 3-Kinases