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. Author manuscript; available in PMC: 2019 Jan 2.
Published in final edited form as: Clin Ther. 2016 Apr 22;38(5):1042–1053. doi: 10.1016/j.clinthera.2016.03.021

Table.

Receptors and roles of well-characterized alarmins.

Alarmins and their receptors Biological activities and functions
AMPs Antimicrobial effects
 Defensins (α, β, and θ) CCR2, CCR6, TLR4 Leukocytes recruitment
 Cathelicidins (eg, LL-37 and CRAMP) FPRL1/FPR2,TLR7, 8, 9 Cytokine induction
 EDN and others TLR2 APC/DC activation
Promotion of immune responses
Inflammation
DNA binding proteins Regulation of gene expression
 HMGN1 TLR4 Leukocytes recruitment
 HMGB1 CXCR4, RAGE, Cytokine induction
 IL-1α TLR2, 4, 7, 8, 9 CD24 APC/DC activation
 IL-33 IL-1R
ST2
Promotion of immune responses
Inflammation
HSP Protein protection
 HSP70, 90, 96 CD14, CD40, CD91, TLR2, 4 scavenger receptors (SRA1) APC/DC activation
Treg polarization
Inflammation
Ion-binding proteins Leukocytes recruitment
 Lactoferrin RAGE, TLR2, 4 Cytokine induction
 S100 A8, A9 RAGE, TLR4 APC/DC activation
Promotion of immune responses
Inflammation
Others Leukocytes recruitment
 ATP and others P2Y2, 6, 12, P2X7 Cytokine induction
APC/DC activation
Inflammation

APC/DC = antigen-presenting cells/dendritic cells; AMP = antimicrobial peptides and proteins; ATP = adenosine triphosphate; CCR = CC chemokine receptor; CD = cluster of differentiation; CRAMP = cathelin-related antimicrobial peptide; CXCR = CXC chemokine receptor; EDN = eosinophil-derived neurotoxin; FPR = formyl peptide receptor; HMGB = High-mobility group protein with a ‘Box’ domain; HMGN = High-mobility group protein with a ‘nucleosome-binding’ domain; IL = interleukin; RAGE = receptor for advanced glycation end-products; TLR = Toll-like receptor; Treg = regulatory T cell.