Journal article
LMP2 immunoproteasome promotes lymphocyte survival by degrading apoptotic BH3-only proteins
D Zanker, K Pang, S Oveissi, C Lu, P Faou, C Nowell, GW Mbogo, S Carotta, C Quillici, G Karupiah, ML Hibbs, SL Nutt, P Neeson, H Puthalakath, W Chen
Immunology and Cell Biology | WILEY | Published : 2018
DOI: 10.1111/imcb.12163
Abstract
The role of the immunoproteasome is perceived as confined to adaptive immune responses given its ability to produce peptides ideal for MHC Class-I binding. Here, we demonstrate that the immunoproteasome subunit, LMP2, has functions beyond its immunomodulatory role. Using LMP2-deficient mice, we demonstrate that LMP2 is crucial for lymphocyte development and survival in the periphery. Moreover, LMP2-deficient lymphocytes show impaired degradation of key BH3-only proteins, resulting in elevated levels of pro-apoptotic BIM and increased cell death. Interestingly, LMP2 is the sole immunoproteasome subunit required for BIM degradation. Together, our results suggest LMP2 has important housekeeping..
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Grants
Awarded by Australian Research Council
Funding Acknowledgements
This project was partly supported by the NHMRC project grants 433608 and 542508 to WC and the NHMRC program grant 567122. DZ was supported by NHMRC biomedical postgraduate scholarship 487926. SLN, MLH and WC are NHMRC Senior Research Fellows. SC is supported by an NHMRC Career Development Award, SLN by an Australian Research Council Future Fellowship and KP is supported by a Melbourne Children's Clinician Scientist Fellowship. The Walter and Eliza Hall Institute is supported by Victorian State Government Operational Infrastructure Support and an Australian Government NHMRC IRIIS.