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In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
Published on: December 30, 2016
Aire and Foxp3 expression in a particular microenvironment for T cell differentiation
Isabelle Hansenne1, Céline Louis, Henri Martens
1Center of Immunology, Institute of Pathology, Liege-Sart Tilman, Belgium.
The autoimmune regulator (Aire) and Foxp3 proteins are found within thymic nurse cells (TNCs), suggesting TNCs play a role in natural regulatory T cell (nTreg) development. This study investigated their expression and localization in TNC/thymocyte complexes.
Area of Science:
- Immunology
- Cell Biology
- Developmental Biology
Background:
- The thymus is crucial for T cell development and self-tolerance.
- Thymic nurse cells (TNCs) provide a unique microenvironment for T cell differentiation.
- The autoimmune regulator (Aire) influences self-antigen expression in the thymus.
Purpose of the Study:
- To investigate the expression and localization of Aire and Foxp3 within TNC/thymocyte complexes.
- To explore the potential role of TNCs in natural regulatory T cell (nTreg) development.
Main Methods:
- Quantitative real-time PCR (RT-qPCR) was used to detect Aire and Foxp3 transcripts in isolated TNC/thymocyte complexes.
- Confocal microscopy and immunocytochemistry were employed to determine the protein localization of Aire and Foxp3.
Main Results:
- Both Aire and Foxp3 transcripts were detected in TNC/thymocyte complexes.
- Foxp3 protein was localized to the nucleus of thymocytes within TNCs.
- Aire protein was primarily found in the cytoplasm of TNCs, with some nuclear presence in associated thymocytes.
Conclusions:
- Aire and Foxp3 are present in the TNC microenvironment, which supports thymic selection.
- The distinct cellular localization of Aire and Foxp3 suggests a role for TNCs in nTreg development.
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