Neutrophils / Neutrophilic Granulocytes are the most common immune cells found where there is inflammation. They were once thought to only have the job of attacking and killing harmful invaders using three main methods: swallowing and destroying them with oxidative stress, releasing substances from their granules, and creating structures called neutrophil extracellular traps (NETs)
However, we now understand that neutrophils are more complex. They are active in gene expression and metabolism, playing roles in both promoting and reducing inflammation. The process of releasing Neutrophil extracellular traps (NETs), known as NETosis, shows this complexity. NETs stick to bacteria to stop them from spreading, directly kill bacteria, and help other immune cells called macrophages to kill bacteria more effectively.
But, if there is too much NETosis, it can harm the body's own tissues, especially during conditions like sepsis and autoimmune diseases. A distinct subset of proinflammatory neutrophils, which are isolated from patients with systemic lupus erythematosus, induces vascular damage and synthesizes type I IFNs. Neutrophils that form nets cause damage to the endothelium, infiltrate tissues, and reveal molecules that stimulate the immune system in systemic lupus erythematosus. The impairment of neutrophil extracellular trap degradation is linked to lupus nephritis.
Neutrophils / Neutrophilic Granulocytes have elegant defense mechanisms to eliminate microbes that have translocated across a single layer of mucosal epithelial cells
During the inflammatory response, neutrophils also contribute to the recruitment of other immune cells and facilitate mucosal healing by releasing mediators necessary for the resolution of inflammation
During inflammation, SCFA stimulate the migration of neutrophils by activating GPR43 and modulate their production of reactive oxygen species and phagocytosis
see also:
Adiposity / Obesity & Inflammation / Inflammatory Diseases
Antimicrobial peptides (AMPs)
Defending the Attack of Pathogens by Neutrophils
Defensins
G-Protein Coupled Receptor 43 (GPR43) & Neutrophils / Neutrophilic Granulocytes
Interferons Type I (IFN Type I)
LL-37 / Cathelicidin antimicrobial peptide
NETosis
Pathogenicity & Staphylococcus aureus
Protegrins
Staphylococcus aureus
Systemic Lupus Erythematosus (SLE)