Macrophage activation by endogenous danger signals
By X. Zhang, DM Mosser. Journal of Pathology, 2008
610 citations recorded by the source corpus.
Subfields: Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/ddf8c4a4d264738175a223f4d8c340dffa9c2e0f
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In Immunology
In Molecular Biology
Citations in the corpus
- Role of Human Macrophage Polarization in Inflammation during Infectious Diseases (2018, background): “Against danger signals, the innate immune system initiates a protective inflammatory response through different phases, from destroying pathogens and removing cellular debris to repairing tissues and maintaining homeostasis [6].”
- Macrophage Phenotypes Regulate Scar Formation and Chronic Wound Healing (2017, background): “Pro-inflammatory mediators interferon-γ (IFN-γ) and tumour necrosis factor (TNF), and damage associated pattern molecules (DAMPs) activate cells to produce ‘classically activated’ M1 macrophages (Figure 1) [11].”
- Macrophages and Tissue Injury: Agents of Defense or Destruction? (2011, background): “Macrophages are essential cellular effectors of the innate immune response, ridding the body of worn-out cells and debris—as well as viruses, bacteria, apoptotic cells, and some tumor cells—and mounting an inflammatory response following injury or infection (2).”
- Exploring the full spectrum of macrophage activation (2008, background): “In many cases the debris from necrosis is loaded with endogenous danger signals, such as heat-shock proteins, nuclear proteins (including HMGB1; high-mobility group box 1 protein), histones, DNA and other nucleotides, and components of the extracellular matrix that are cleaved by cellular protease”
- The role of defective clearance of apoptotic cells in systemic autoimmunity (2010, background): “Nucleic acids, various proteins, metabolic intermediates and active, inflammatory cytokines are well accepted danger signals released by primary necrotic cells”
- Damage-Associated Molecular Patterns in Inflammatory Diseases (2018, background): “These DAMPs are recognized by macrophages, and inflammatory responses are triggered by different pathways, including TLRs and inflammasomes (10,11).”