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RelB as a master regulator of the thymic medulla: characterization of factors that control RelB expression and the role of the RelB target gene Enpp2/Atx

Applicant Professor Dr. Christoph Englert, since 11/2014
Subject Area Cell Biology
Immunology
Term from 2009 to 2018
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 154810081
 
Final Report Year 2018

Final Report Abstract

The initial goal of this grant was to better understand the regulation of RelB, the master regulator of mTEC development. The data that were generated in the context of this proposal show that classical NF-κB signaling, which leads to the activation of RelA and c-Rel is as essential for mTEC development as the alternative pathway which activates RelB. Furthermore, the results showed that the role of RelA and c-Rel is to upregulate the transcription of RelB by directly binding to the Relb promoter. Analyses of appropriate reporter mice further demonstrated that both NF-κB activity and RelB expression are mainly confined to mature mTECs, corroborating the link between both events in these cells. Thus, these data reveal a crosstalk mechanism between classical and alternative NF-κB pathways that tightly controls the development of mature mTECs to ensure self-tolerance. Analysis of thymic endothelial and mesenchymal cells from RelBnull mice by FACS revealed no further essential role for RelB in the development of the thymic stroma.

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