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Established IL-2-dependent double-negative (CD4- CD8-) TCRαβ/CD3+ ATL cells: induction of CD4 expression
Authors:Yasuaki  Yamada   Masatoshi  Fujita   Haruhiko  Suzuki   Sunao  Atogami   Hisashi  Sohda   Ken  Murata   Kunihiro  Tsukasaki   Saburo  Momita   Tomoko  Kohno   Takahiro  Maeda   Tatsuroh  Joh   Shimeru  Kamihira   Hiroshi  Shiku   Masao  Tomonaga
Affiliation:Department of Haematology, Atomic Disease Institute, Sakamoto-machi, Nagasaki;Department of Oncology, Nagasaki University School of Medicine, Sakamoto-machi, Nagasaki;Department of Blood Transfusion Service, Nagasaki University Hospital, Sakamoto-machi, Nagasaki, Japan
Abstract:Summary. We established IL-2-dependent T cells from an adult T-cell leukaemia (ATL) patient whose leukaemic cells changed from CD4 single-p-positive in the initial phase to double-negative (CD4- CD8-) at the time of exacerbation. The cells termed SO-4 were of ATL cell origin and showed the double-negative TCRαβ/CD3+ T-cell phenotype. SO-4 cells acquired CD4 antigen expression following stimulation with concanavlin A (ConA) or immobilized anti-CD3 antibody. The induction was inhibited by herbimycin A, an inhibitor of protein tyrosine kinase (PTK) activity. No CD4 mRNA was detectable in unstimulated SO-4 cells but a 3.0 kb signal specific for CD4 mRNA was detected after stimulation. These findings indicate that SO-4 cells return to their original phenotype (CD4 single-positive) by stimulation involving PTK. The results indicate that there is a pathway of phenotypic cycling between CD4 single-positive and double-negative T cells.
Keywords:ATL    HTLV-I    phenotype    CD4    IL-2
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