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Updated: Jun 30, 2026

Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
Published on: April 16, 2015
Expression and role of interleukin-2 receptor beta chain on CD4-CD8- T cell receptor alpha beta+ cells [corrected]
Y Takeuchi1, T Tanaka, K Hamamura
1Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Insights
Interleukin-2 receptor beta (IL-2R beta) is expressed on specific mouse thymocytes and its role in CD4-CD8-TCR alpha beta+ cell development is complex, not solely IL-2 dependent.
Area of Science:
- Immunology
- Developmental Biology
- Cell Biology
Background:
- The interleukin-2 receptor beta chain (IL-2R beta) plays a crucial role in immune responses.
- Understanding IL-2R beta expression patterns is key to deciphering T cell development and function.
Purpose of the Study:
- To investigate the expression of IL-2R beta on murine thymocyte subpopulations.
- To determine the functional role of IL-2R beta in the development of CD4-CD8-TCR alpha beta+ cells.
Main Methods:
- Utilized anti-murine IL-2R beta monoclonal antibody (mAb) for expression analysis.
- Employed fetal thymus organ culture and in vivo blockade experiments to assess IL-2/IL-2R pathway function.
Main Results:
- IL-2R beta is constitutively expressed on a small subset of thymocytes, with developmentally regulated expression patterns.
- Expression shifts from T cell receptor gamma delta+ (TcR gamma delta+) cells in fetal mice to CD4-CD8-TcR alpha beta+ thymocytes in adults.
- IL-2R beta is functional in CD4-CD8-TcR alpha beta+ thymocyte expansion in vitro, but in vivo IL-2/IL-2R blockade does not affect their development.
Conclusions:
- IL-2R beta expression is developmentally regulated on murine thymocytes.
- While IL-2R beta is involved in the expansion of CD4-CD8-TcR alpha beta+ cells, IL-2 signaling is not the sole determinant of their development.
Abstract:
Using anti-murine interleukin-2 receptor beta chain (IL-2R beta) monoclonal antibody (mAb), we have examined the expression of IL-2R beta on murine thymocyte subpopulations. We found that it was constitutively expressed on 1%-4% of thymocytes in an almost mutually exclusive fashion with IL-2R alpha. The expression of IL-2R beta is developmentally regulated. While it is expressed mainly on T cell receptor gamma delta+ (TcR gamma delta+) cells during fetal age, the major subpopulation expressing IL-2R beta in adult mouse shifts to CD4-CD8-TcR alpha beta+ thymocytes. A considerable portion of CD4-CD8- TcR alpha beta+ cells in other organs, including spleen, bone marrow and liver, was also found to express IL-2R beta. In fetal thymus organ culture, the above thymocyte subset was induced to expand in response to exogeneous IL-2, and the expansion was inhibited by addition of anti-IL-2R beta mAb, suggesting that IL-2R beta is functional in this subpopulation. However, in vivo blockade of the IL-2/IL-2R pathway with the mAb did not exert any effects on the appearance of CD4-CD8- TcR alpha beta+ cells both in the thymus and the periphery. This indicates that the development of CD4-CD8- TcR alpha beta+ cells is not solely controlled by IL-2 but also by other complex elements.
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