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Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors

Freshly isolated CD8(+) T cells, but not CD4(+) T cells, contained 20–30% of asialo GM1(+) (ASGM1(+)) T cells which were distinct from ASGM1(+)NK1.1(+) natural killer cells. This novel ASGM1(+)CD8(+) T cell subpopulation showed a strong proliferative response to interlenkin‐12 (IL‐12) in the presenc...

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Detalles Bibliográficos
Autores principales: Lee, Ushaku, Santa, Kazuki, Habu, Sonoko, Nishimura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921113/
https://www.ncbi.nlm.nih.gov/pubmed/8641977
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00241.x
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author Lee, Ushaku
Santa, Kazuki
Habu, Sonoko
Nishimura, Takashi
author_facet Lee, Ushaku
Santa, Kazuki
Habu, Sonoko
Nishimura, Takashi
author_sort Lee, Ushaku
collection PubMed
description Freshly isolated CD8(+) T cells, but not CD4(+) T cells, contained 20–30% of asialo GM1(+) (ASGM1(+)) T cells which were distinct from ASGM1(+)NK1.1(+) natural killer cells. This novel ASGM1(+)CD8(+) T cell subpopulation showed a strong proliferative response to interlenkin‐12 (IL‐12) in the presence of IL‐2. Culture of ASGM1(+)CD8(+) T cells with IL‐12 plus IL‐2 allowed the generation of anomalous killer T cells concomitantly with the accumulation of cytolytic molecules. Moreover, ASGM1(+)CD8(+) T cells produced high levels of interferon‐γ (IFN‐γ), but not IL‐4, upon stimulation with IL‐12 plus IL‐2. Such immune responses were not observed in ASGM1(−) CD8(+) T cell snbpopulations constituting the majority of CD8(+) T cells. These results demonstrated that ASGM1(+)CD8(+) T cells are a novel subpopulation of IL‐12‐responsive and IFN‐γ‐producing killer T cell precursors.
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spelling pubmed-59211132018-05-11 Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors Lee, Ushaku Santa, Kazuki Habu, Sonoko Nishimura, Takashi Jpn J Cancer Res Rapid Communication Freshly isolated CD8(+) T cells, but not CD4(+) T cells, contained 20–30% of asialo GM1(+) (ASGM1(+)) T cells which were distinct from ASGM1(+)NK1.1(+) natural killer cells. This novel ASGM1(+)CD8(+) T cell subpopulation showed a strong proliferative response to interlenkin‐12 (IL‐12) in the presence of IL‐2. Culture of ASGM1(+)CD8(+) T cells with IL‐12 plus IL‐2 allowed the generation of anomalous killer T cells concomitantly with the accumulation of cytolytic molecules. Moreover, ASGM1(+)CD8(+) T cells produced high levels of interferon‐γ (IFN‐γ), but not IL‐4, upon stimulation with IL‐12 plus IL‐2. Such immune responses were not observed in ASGM1(−) CD8(+) T cell snbpopulations constituting the majority of CD8(+) T cells. These results demonstrated that ASGM1(+)CD8(+) T cells are a novel subpopulation of IL‐12‐responsive and IFN‐γ‐producing killer T cell precursors. Blackwell Publishing Ltd 1996-05 /pmc/articles/PMC5921113/ /pubmed/8641977 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00241.x Text en
spellingShingle Rapid Communication
Lee, Ushaku
Santa, Kazuki
Habu, Sonoko
Nishimura, Takashi
Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title_full Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title_fullStr Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title_full_unstemmed Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title_short Murine Asialo GM1(+)CD8(+) T Cells as Novel Interleukin‐12‐responsive Killer T Cell Precursors
title_sort murine asialo gm1(+)cd8(+) t cells as novel interleukin‐12‐responsive killer t cell precursors
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921113/
https://www.ncbi.nlm.nih.gov/pubmed/8641977
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00241.x
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