Table 1.
DAMP receptors | DAMPs | Expression pattern | Main effect | Refs |
---|---|---|---|---|
TLR | Ubiquitous, high in immune cells | Promote the expression of pro-inflammatory genes, thus upregulate the production of cytokines, chemokines, and adhesion molecules. | (Yu et al., 2010; Lin et al., 2011; Vidya et al., 2018; Gong et al., 2020) | |
TLR2 | HMGB1, HSP60, HSP70, histone | |||
TLR4 | HMGB1, HSP22, HSP60, HSP70, HSP72, histone | |||
TLR9 | DNA, HMGB1 | |||
NLRP3 | ATP | DCs, neutrophils, monocytes and macrophages | Promote the activation of caspase-1. Increase the secretion of IL-1β and IL-18. Initiate pyroptosis. | (Sutterwala et al., 2006; Jin and Flavell, 2010; Mangan et al., 2018; Gong et al., 2020) |
RAGE | HMGB1 | Ubiquitous, high in T cells, B cells, and macrophages | Promote the expression of pro-inflammatory genes. Mediate cell migrationand apoptosis. | (Chuah et al., 2013; Hudson and Lippman, 2018; Gong et al., 2020) |
P2X7R (G protein-coupled receptor) |
ATP | Ubiquitous | Promote the release of cytokine and chemokine, the activation of NLRP3 inflammasome, transcription factor and T cells. | (Di Virgilio et al., 2017b; Adinolfi et al., 2018; Martínez-García et al., 2019; Gong et al., 2020) |
P2Y2R (ion channel) |
ATP | Ubiquitous, high in immune cells, epithelial and endothelial cells | Promote the migration, and activation of immune cells. Control iron channels. | (Xu et al., 2018; Gong et al., 2020) |