EFFECTS OF MACROPHAGE INFLAMMATORY $PROTEIN-1{\alpha}$ON THE T CELL PROLIFERATION AND THE EXPRESSION OF CD4 AND CD8

Macrophage Inflammatory Protein $1{\alpha}$가 T세포성장 및 CD4, CD8 발현에 미치는 영향

  • Choi, Jong-Sun (Department of Oral and Maxillofacial Surgery, College of Dentistry, Chonbuk National University) ;
  • Kim, Oh-Whan (Department of Oral and Maxillofacial Surgery, College of Dentistry, Chonbuk National University)
  • 최종선 (전북대학교 치과대학 구강악안면외과학 교실) ;
  • 김오환 (전북대학교 치과대학 구강악안면외과학 교실)
  • Published : 1996.03.31

Abstract

Macrophage inflammatory protein $(MIP)-1{\alpha}$ is a cytokine which produces wide range of bioactivities such as proinflammatory, immunomodulatory, and hematopoietic modulatory actions. To determine whether $MIP-1{\alpha}$ acts as a negative regulator on the functions of lymphocyte, $[^3H]$-thymidine incorporation test and flow cytometric analysis were performed by using human tonsil T cell, human peripheral blood T cell, and murine cytolytic T lymphocyte (CTL) line CTLL-2, The results were as follow. 1. When human tonsil T lymphocytes were stimulated with anti-CD3 monoclonal antibody (mAb), rate of T cell proliferation was about four times increased. 200ng/ml of $MIP-1{\alpha}$ inhibited anti-CD3 mAb-mediated T cell growth as much as 60% (P<0.05). 2. The suppression of human peripheral T cell proliferation produced by $MIP-1{\alpha}$ was dramatic, but variable among T cells derived from different individuals $(40%{\sim}90%)$. 3. $MIP-1{\alpha}$inhibited the proliferation of murine CTL line CTLL-2 as much as 75%(P<0.001). 4. When the $MIP-1{\alpha}$ was added to human peripheral T cell, cell proporation of $CD4^+$ helper T cell and $CD8^+$ CTL were not noticeably affected. The expression level of CD4, not of Cd8, however, was down regulated by $MIP-1{\alpha}$ treatment $(27%{\sim}82%)$.

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