Autophagy is an inflammation-related defensive mechanism against disease

• Published in: Advances in experimental medicine and biology Vol. 824; p. 43
• Main Authors: Joven, Jorge, Guirro, Maria, Mariné-Casadó, Roger, Rodríguez-Gallego, Esther, Menéndez, Javier A
• Format: Journal Article
• Language: English
• Published: United States 01.01.2014
• Subjects: Animals; Autophagy - immunology; Cytokines - immunology; Cytokines - metabolism; Humans; Immunity, Innate; Inflammation - immunology; Inflammation - metabolism; Inflammation - pathology; Obesity - immunology; Obesity - metabolism; Obesity - pathology
• ISSN: 0065-2598
• DOI: 10.1007/978-3-319-07320-0_6

The inflammatory response is an energy-intensive process. Consequently, metabolism is closely associated with immune function. The autophagy machinery plays a role in metabolism by providing energy but may also be used to attack invading pathogens (xenophagy). The autophagy machinery may function to protect against not only the threats of infection but also the threats of the host's own response acting on the central immunological tolerance and the negative regulation of innate and inflammatory signaling. The balance between too little and too much autophagy is critical for the survival of immune cells because autophagy is linked to type 2-cell death programmed necrosis and apoptosis. Changes in inflammatory cells are driven by extracellular signals; however, the mechanisms by which cytokines mediate autophagy regulation and govern immune cell function remain unknown. Certain cytokines increase autophagy, whereas others inhibit autophagy. The relationship between autophagy and inflammation is also important in the pathogenesis of metabolic, non-communicable diseases. Inflammation per se is not the cause of obesity-associated diseases, but it is secondary to both the positive energy balance and the specific cellular responses. In metabolic tissues, the suppression of autophagy increases inflammation with the overexpression of cytokines, resulting in an activation of autophagy. The physiological role of these apparently contradictory findings remains uncertain but exemplifies future challenges in the therapeutic modulation of autophagy in the management of disease.