Table 1.
LL-37 functions in innate immunity.
Antimicrobial agent | Protection against gram-positive and negative bacteria. | [15,16] |
Protection to infection | LL-37 lowers the permeability of epithelial cells inhibiting the entry of microorganisms to them. | [5] |
Chemokine function | LL-37 modulates and stimulates the function of monocytes, lymphocytes, neutrophils and mastocytes. | [54] |
Wound healing | Reepithelization and scarring by transactivation of epidermal growth factor receptor, inducing keratinocytes migration. | [19] |
Improves coestimulation | High concentrations of LL-37 induce a higher expression of membrane CD86. | [52] |
Enhance type I IFN response | LL-37 delivers dsRNA to TLR3 with their agonist poly(I:C) which produces the transcription of NF-kB and IRF3 and enhances the type I IFN response. | [22] |
Prevention of sepsis | LL-37 binds to LPS to prevent the activation of TLR4. | [31] |
Delivers plasmids to the nuclei | It prevents the degradation of plasmids from nucleases and form complexes with the DNA to deliver them to the nuclei by lipid rafts to stimulate TLR7 and TLR9. | [55] |
Enhances the function of dendritic cells | Dendritic cells derived from stimuli of LL-37 show a better capacity of endocytic capacity, high concentrations of phagocytic receptors, high concentrations of coestimulation molecules and high levels of type I IFN secretion which stimulates a better Th1 response against viruses and bacteria. | [53,56] |
Abbreviations: Double-stranded ribonucleic acid (dsRNA), Toll-like receptor (TLR), lipopolysaccharide (LPS), nuclear factor K–B (NF-kB), Polyinosinic: polycytidylic acid (poly(I:C)), interferon regulatory factor 3 (IRF3).