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Mechanisms of unconventional secretion of IL-1 family cytokines.
- Source :
-
Cytokine [Cytokine] 2015 Aug; Vol. 74 (2), pp. 213-8. Date of Electronic Publication: 2015 Apr 25. - Publication Year :
- 2015
-
Abstract
- One of the most poorly understood processes in cell biology is the peculiar ability of specific leaderless proteins to be secreted via ER/Golgi-independent mechanisms ('unconventional protein secretion'). One such leaderless protein is the major immune-activating cytokine, interleukin-1β (IL-1β). Unusual amongst cytokines, IL-1β is expressed in the cytosol as an inactive precursor protein. It requires maturation by the caspase-1 protease, which itself requires activation upon immune cell sensing of infection or cell stress. Despite 25 years of intensive research into IL-1β secretory mechanisms, how it exits the cell is still not well understood. Here we will review the various mechanisms by which macrophages have been proposed to secrete IL-1 family cytokines, and the potential involvement of caspase-1 therein. Since aberrant IL-1β production drives inherited and acquired human diseases (e.g. autoinflammatory diseases, arthritic diseases, gout, Alzheimer's disease), elucidation of the IL-1β secretory pathway may offer new therapeutic opportunities for treatment across this wide range of human conditions.<br /> (Copyright © 2015 Elsevier Ltd. All rights reserved.)
- Subjects :
- Alzheimer Disease metabolism
Alzheimer Disease pathology
Animals
Arthritis metabolism
Arthritis pathology
Caspase 1 metabolism
Gout metabolism
Gout pathology
Humans
Interleukin-1beta metabolism
Macrophages metabolism
Macrophages pathology
Alzheimer Disease immunology
Arthritis immunology
Caspase 1 immunology
Gout immunology
Interleukin-1beta immunology
Macrophages immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0023
- Volume :
- 74
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cytokine
- Publication Type :
- Academic Journal
- Accession number :
- 25922276
- Full Text :
- https://doi.org/10.1016/j.cyto.2015.03.022