| Literature DB >> 29530410 |
Ulf Andersson1, Huan Yang2, Helena Harris3.
Abstract
Alarmins are preformed, endogenous molecules that can be promptly released to signal cell or tissue stress or damage. The ubiquitous nuclear molecule high-mobility group box 1 protein (HMGB1) is a prototypical alarmin activating innate immunity. HMGB1 serves a dual alarmin function. The protein can be emitted to alert adjacent cells about endangered homeostasis of the HMGB1-releasing cell. In addition to this expected path of an alarmin, extracellular HMGB1 can be internalized via RAGE-receptor mediated endocytosis to the endolysosomal compartment while attached to other extracellular proinflammatory molecules. The endocytosed HMGB1 may subsequently destabilize lysosomal membranes. The HMGB1-bound partner molecules depend on the HMGB1-mediated transport and the induced lysosomal leakage to obtain access to endosomal and cytosolic reciprocal sensors to communicate extracellular threat and to initiate the proper activation pathways.Entities:
Keywords: Alarmins; DAMPs; HMGB1; Inflammation; RAGE; Sepsis; TLR4; Trauma
Mesh:
Substances:
Year: 2018 PMID: 29530410 DOI: 10.1016/j.smim.2018.02.011
Source DB: PubMed Journal: Semin Immunol ISSN: 1044-5323 Impact factor: 11.130