Alternative pathway for the development of Vα 14+ NKT cells directly from CD4-CD8- thymocytes that bypasses the CD4+ CD8+ stage

Nyambayar Dashtsoodol, Tomokuni Shigeura, Minako Aihara, Ritsuko Ozawa, Satoshi Kojo, Michishige Harada, Takaho A. Endo, Takashi Watanabe, Osamu Ohara, Masaru Taniguchi

研究成果: ジャーナルへの寄稿学術誌査読

36 被引用数 (Scopus)

抄録

Although invariant V α 14 + natural killer T cells (NKT cells) are thought to be generated from CD4 + CD8 + double-positive (DP) thymocytes, the developmental origin of CD4 - CD8 - double-negative (DN) NKT cells still remains unresolved. Here we provide definitive genetic evidence obtained, through studies of mice with DP-stage-specific ablation of expression of the gene encoding the recombinase component RAG-2 (Rag2) and by a fate-mapping approach, that supports the proposal of the existence of an alternative developmental pathway through which a fraction of DN NKT cells with strong T-helper-type-1 (T H 1)-biased and cytotoxic characteristics develop from late DN-stage thymocytes, bypassing the DP stage. These findings provide new insight into understanding of the development of NKT cells and propose a role for timing of expression of the invariant T cell antigen receptor in determining the functional properties of NKT cells.

本文言語英語
ページ(範囲)274-282
ページ数9
ジャーナルNature Immunology
18
3
DOI
出版ステータス出版済み - 2月 15 2017
外部発表はい

!!!All Science Journal Classification (ASJC) codes

  • 免疫アレルギー学
  • 免疫学

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