| ID | Sequence | Length | GC content |
|---|---|---|---|
| ACAAACUUUCAGAGACAGCAGAGCACACAAGCUUCUAGGACAAGAGCCA… | 1642 nt | 0.3289 | |
| ACAAACUUUCAGAGACAGCAGAGCACACAAGCUUCUAGGACAAGAGCCA… | 2058 nt | 0.3222 |
The protein encoded by this gene is a member of the CXC chemokine family and is a major mediator of the inflammatory response. The encoded protein is commonly referred to as interleukin-8 (IL-8). IL-8 is secreted by mononuclear macrophages, neutrophils, eosinophils, T lymphocytes, epithelial cells, and fibroblasts. It functions as a chemotactic factor by guiding the neutrophils to the site of infection. Bacterial and viral products rapidly induce IL-8 expression. IL-8 also participates with other cytokines in the proinflammatory signaling cascade and plays a role in systemic inflammatory response syndrome (SIRS). This gene is believed to play a role in the pathogenesis of the lower respiratory tract infection bronchiolitis, a common respiratory tract disease caused by the respiratory syncytial virus (RSV). The overproduction of this proinflammatory protein is thought to cause the lung inflammation associated with csytic fibrosis. This proinflammatory protein is also suspected of playing a role in coronary artery disease and endothelial dysfunction. This protein is also secreted by tumor cells and promotes tumor migration, invasion, angiogenesis and metastasis. This chemokine is also a potent angiogenic factor. The binding of IL-8 to one of its receptors (IL-8RB/CXCR2) increases the permeability of blood vessels and increasing levels of IL-8 are positively correlated with increased severity of multiple disease outcomes (eg, sepsis). This gene and other members of the CXC chemokine gene family form a gene cluster in a region of chromosome 4q. [provided by RefSeq, May 2020]
A study in humans demonstrated that serum CXCL8 levels were significantly increased in patients with sepsis compared to healthy controls and showed a positive correlation with the CXCL8 and other inflammatory markers [Xu et al. DOI:10.3892/mmr.2022.12850]. A study in pigs demonstrated that in a combined trauma model, local IL-8 levels in fracture hematoma were significantly higher than systemic serum levels, but these local levels were attenuated in the hypothermic trauma group compared to the normothermic group, while systemic IL-8 was significantly higher in the hypothermic group at 48 hours [Horst et al. DOI:10.1371/journal.pone.0154788]. In human skin after thermal injury, microarray analysis identified IL-8 as a validated pro-inflammatory cytokine gene that was highly expressed, peaking in the middle wound healing period (4-7 days post-burn) [Greco et al. DOI:10.1016/j.burns.2009.06.211].