Table 1.
PMN effector function | Contribution to IBD pathology | Association with MPs | References |
---|---|---|---|
ROS | Contribute to oxidative stress, base damage/modification, replication errors, and single-strand breaks. | No | Nguyen et al. (2017), Cadet and Wagner (2013), Kellner et al. (2017), Cadet et al. (2017) |
Myeloperoxidase | Generate ROS, promote cells death, and impede wound healing. | Yes | Slater et al. (2017) |
Metalloproteinases | Disrupt tissue integrity, increase epithelial and vascular permeability, and immune cell recruitment. | Yes | Butin-Israeli et al. (2016) |
Cytokines | Immune cells recruitment and inflammatory polarization, impede wound healing. | TBD | Wera et al. (2016), Wright et al. (2010), Wang et al. (2018) |
miRNAs (miR-23a/-155, miR-9) | Posttranscriptionally regulate signaling pathways. | Yes | Butin-Israeli et al. (2019), Distler et al. (2005) |
The table summarizes the pathological effector functions of PMNs and their association with MPs as it relates to IBD.
IBD, inflammatory bowel disease; MP, microparticles; PMN, neutrophil; ROS, reactive oxygen species; TBD, to be determined.