A new cryptic cationic antimicrobial peptide from human apolipoprotein E with antibacterial activity and immunomodulatory effects on human cells. (20th April 2016)

• Record Type: Journal Article
• Authors: Pane, Katia; Sgambati, Valeria; Zanfardino, Anna; Smaldone, Giovanni; Cafaro, Valeria; Angrisano, Tiziana; Pedone, Emilia; Di Gaetano, Sonia; Capasso, Domenica; Haney, Evan F.; Izzo, Viviana; Varcamonti, Mario; Notomista, Eugenio; Hancock, Robert E.W.; Di Donato, Alberto; Pizzo, Elio
• Is Part Of: FEBS journal. Volume 283:Number 11(2016)
• Page Start: 2115
• Page End: 2131
• Publication Date: 2016-04-20
• Subjects: antimicrobial peptides -- apolipoprotein E -- immunomodulation -- inflammation -- lipopolysaccharide; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 572
• DOI: 10.1111/febs.13725
• Languages: English
• ISSNs: 1742-464X

Abstract

Abstract : Cationic antimicrobial peptides (AMPs) possess fast and broad‐spectrum activity against both Gram‐negative and Gram‐positive bacteria, as well as fungi. It has become increasingly evident that many AMPs, including those that derive from fragments of host proteins, are multifunctional and able to mediate various immunomodulatory functions and angiogenesis. Among these, synthetic apolipoprotein‐derived peptides are safe and well tolerated in humans and have emerged as promising candidates in the treatment of various inflammatory conditions. Here, we report the characterization of a new AMP corresponding to residues 133–150 of human apolipoprotein E. Our results show that this peptide, produced either by chemical synthesis or by recombinant techniques in Escherichia coli, possesses a broad‐spectrum antibacterial activity. As shown for several other AMPs, ApoE (133–150) is structured in the presence of TFE and of membrane‐mimicking agents, like SDS, or bacterial surface lipopolysaccharide (LPS), and an anionic polysaccharide, alginate, which mimics anionic capsular exo‐polysaccharides of several pathogenic microorganisms. Noteworthy, ApoE (133–150) is not toxic toward several human cell lines and triggers a significant innate immune response, assessed either as decreased expression levels of proinflammatory cytokines in differentiated THP‐1 monocytic cells or by the induction of chemokines released from PBMCs. This novel bioactive AMP also showed a significant anti‐inflammatory effect on human keratinocytes, suggesting its potential use as a model for designing new immunomodulatory therapeutics. Abstract : Antimicrobial peptides (AMPs) mediate various immunomodulatory functions. We report a new AMP corresponding to residues 133–150 of human apolipoprotein E which is structured in the presence of SDS or LPS, possesses broad‐spectrum antibacterial activity, is not toxic toward several human cell lines, and triggers a significant innate immune response. This AMP could thus be used for designing new immunomodulatory therapeutics.