IL-2 independent transformation of a unique human T cell line, TY8-3, and its subclones by HTLV-I and -II

Int J Cancer. 2001 Jan 1;91(1):99-108. doi: 10.1002/1097-0215(20010101)91:1<99::aid-ijc1016>3.0.co;2-o.

Abstract

Human T cell leukemia virus type I (HTLV-I) is etiologically associated with adult T cell leukemia (ATL) and chronic neurological disease, tropical spastic paraparesis (TSP). In our study, a unique IL-2 dependent human T cell line, designated TY8-3, was established from a thymoma obtained from a myasthenia gravis patient. The cells were heterogeneous and mainly consisted of those with CD4 , CD8 as well as activation markers and adhesion molecules including IL-2Ralpha,beta,gamma, CD45RO, Tf-R, HLA-DR, LFA-1alpha,beta, LFA-3, ICAM-1 and OX40 but without CD3 surface markers. Furthermore, these cells underwent an efficient and reproducible IL-2 independent transformation upon cocultivation with HTLV-I/II producing cell lines. Interestingly, although the infected cells became IL-2 independent, the growth rate of infected cells was significantly lower than those of parental TY8-3 cells. Clonal HTLV-I proviral DNA and viral particles were detected in the cells. Down-regulation of the lck and fyn genes and activation of the lyn gene was demonstrated in the IL-2 independent HTLV-positive TY8-3 cells. Subclones of TY8-3 cells were again able to be efficiently transformed and became IL-2 independent several months after coculture. Our results thus exhibit that TY8-3 cells and its subclones provide us with a very unique model whereby IL-2 independent transformation events of human T cells by HTLV-I/II in vitro can be studied at a clonal level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD4 Antigens / metabolism
  • CD8 Antigens / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cell Culture Techniques*
  • Cell Division
  • Cell Line
  • Cell Line, Transformed*
  • Coculture Techniques
  • Down-Regulation
  • Flow Cytometry
  • Fluorescent Antibody Technique, Indirect
  • Human T-lymphotropic virus 1 / metabolism*
  • Human T-lymphotropic virus 2 / metabolism*
  • Humans
  • Interleukin-2 / metabolism*
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck) / genetics
  • Microscopy, Electron
  • Myasthenia Gravis / metabolism
  • Phenotype
  • Protein-Tyrosine Kinases / genetics
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-fyn
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocytes / metabolism*
  • Thymoma / metabolism
  • Time Factors
  • src-Family Kinases

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Cell Adhesion Molecules
  • Interleukin-2
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Protein-Tyrosine Kinases
  • FYN protein, human
  • Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
  • Proto-Oncogene Proteins c-fyn
  • lyn protein-tyrosine kinase
  • src-Family Kinases