Furthermore, our results clearly indicate that the regulation of NF-κB activity by CYLD in thymocytes depends primarily on IKK2, and IKK1 cannot compensate for the loss of IKK2 in thymocytes with inactive CYLD. In this respect, our results provide

a definitive proof of the functional association between CYLD and IKK2 and they are consistent with the demonstration of IKK2 hyperactivation in peripheral T cells bearing Selleckchem PF-6463922 null Cyld alleles 11. On the other hand, the LckCre-Cyldflx9/flx9-Ikk2flx/flx mice exhibited a much more severe defect in the representation of peripheral T-cell populations than the one observed in LckCre-Ikk2flx/flx mice, despite the restoration of thymocyte development. Actually, the double mutant mice exhibited a dramatic loss of both CD4+ and CD8+ cells. This finding reflects an IKK2-independent role of CYLD in the establishment of physiological peripheral T-cell populations. CYLD may have an antiapoptotic selleck inhibitor role in peripheral T cells by preventing

their excessive activation. This would be consistent with the reported hyperactive phenotype of peripheral T cells bearing null Cyld alleles 11. Alternatively, a role for functional CYLD in the process of mature thymocyte egress to the periphery cannot be excluded. In summary, our data identified a thymocyte-instrinsic role for the deubiqutinating activity of CYLD in establishing the appropriate level Methamphetamine of IKK2-mediated NF-κB activity and associated physiological thymocyte selection. Furthermore, our experiments revealed an IKK2-independent role for the deubquitinating activity of CYLD in establishing normal peripheral T-cell populations. The generation of mice with loxP-targeted Cyld locus has been described previously 26. The transgenic Lck-Cre27 mice were provided by J. D. Marth (University of California, San Diego, USA). All mice were maintained in mixed C57Bl/6, 129Ola background. The mice were bred and maintained

in the animal facilities of the Biomedical Sciences Research Centre ‘Alexander Fleming’ under specific-pathogen-free conditions. Experiments on live animals were approved by the Hellenic Ministry of Rural Development (Directorate of Veterinary Services, approval ID: 3926/261009) and by Biomedical Sciences Research Center ‘Al. Fleming’s’ Animal Research and Ethics Committee for compliance to FELASA regulations. Screening of tail DNA for inheritance of the floxed Cyld gene was performed by PCR using the following primers: F6: 5′-CGTGAACAGATGTGAAGGC-3′; R6: 5′-CTACCATCCCTGCTAACCAC-3′; F5: 5′-GCAGGCTGTACAGATGGAAC-3′; R1: 5′-CTGCAAATTTCAGGTTGCTGTTG-3′. Inheritance of the LckCre transgene was determined by PCR using the following primers: forward, 5′-ATTACCGGTCGATGCAACGAGT-3′ and reverse, 5′-CAGGTATCTCTGACCAGAGTCA-3′.