| Literature DB >> 27959619 |
Kajal Hamidzadeh1, Stephen M Christensen1, Elizabeth Dalby1, Prabha Chandrasekaran1, David M Mosser1.
Abstract
In recent years, researchers have devoted much attention to the diverse roles of macrophages and their contributions to tissue development, wound healing, and angiogenesis. What should not be lost in the discussions regarding the diverse biology of these cells is that when perturbed, macrophages are the primary contributors to potentially pathological inflammatory processes. Macrophages stand poised to rapidly produce large amounts of inflammatory cytokines in response to danger signals. The production of these cytokines can initiate a cascade of inflammatory mediator release that can lead to wholesale tissue destruction. The destructive inflammatory capability of macrophages is amplified by exposure to exogenous interferon-γ, which prolongs and heightens inflammatory responses. In simple terms, macrophages can thus be viewed as incendiary devices with hair triggers waiting to detonate. We have begun to ask questions about how these cells can be regulated to mitigate the collateral destruction associated with macrophage activation.Entities:
Keywords: NF-κB; TLR; adenosine; cytokines; prostaglandin; transcription
Mesh:
Substances:
Year: 2016 PMID: 27959619 PMCID: PMC5912892 DOI: 10.1146/annurev-physiol-022516-034348
Source DB: PubMed Journal: Annu Rev Physiol ISSN: 0066-4278 Impact factor: 19.318