Autophagy and cytokines

作者：Harris James^*

来源：Cytokine, 2011, 56(2): 140-144.

DOI：10.1016/j.cyto.2011.08.022

• Inflammasome
• Mycobacteria
• Th1
• Th2
• Th17

Autophagy is a highly conserved homoeostatic mechanism for the lysosomal degradation of cytosolic constituents, including long-lived macromolecules, organelles and intracellular pathogens. Autophagosomes are formed in response to a number of environmental stimuli, including amino acid deprivation, but also by both host- and pathogen-derived molecules, including toll-like receptor ligands and cytokines. In particular, IFN-gamma, TNF-alpha, IL-1, IL-2, IL-6 and TGF-beta have been shown to induce autophagy, while IL-4, IL-10 and IL-13 are inhibitory. Moreover, autophagy can itself regulate the production and secretion of cytokines, including IL-1, IL-18, TNF-alpha, and Type I IFN. This review discusses the potentially pivotal roles of autophagy in the regulation of inflammation and the coordination of innate and adaptive immune responses.

• 出版日期2011-11