4.8 Review

Proteolytic Processing of Interleukin-1 Family Cytokines: Variations on a Common Theme

期刊

IMMUNITY
卷 42, 期 6, 页码 991-1004

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2015.06.003

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资金

  1. Fund for Scientific Research Flanders (FWO) [G028712N, G046612N, G016413N, G027413N, G090914N]
  2. Belgian Foundation Against Cancer
  3. Agency for Innovation by Science and Technology
  4. Interuniversity Attraction Poles [P7/32]
  5. Belgian Science Policy (Belgian Coordinated Collections of Microorganisms [BCCM]/LMBP)
  6. Ghent University [BOF13-GOA-005]
  7. FWO
  8. IWT

向作者/读者索取更多资源

Members of the extended interleukin-1 (IL-1) cytokine family, such as IL-1, IL-18, IL-33, and IL-36, play a pivotal role in the initiation and amplification of immune responses. However, deregulated production and/or activation of these cytokines can lead to the development of multiple inflammatory disorders. IL-1 family members share a broadly similar domain organization and receptor signaling pathways. Another striking similarity between IL-1 family members is the requirement for proteolytic processing in order to unlock their full biological potential. Although much emphasis has been put on the role of caspase-1, another emerging theme is the involvement of neutrophil-and mast cell-derived proteases in IL-1 family cytokine processing. Elucidating the regulation of IL-1 family members by proteolytic processing is of great interest for understanding inflammation and immunity. Here, we review the identity of the proteases involved in the proteolytic processing of IL-1 family cytokines and the therapeutic implications in inflammatory disease.

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