Regulation of macrophage-associated inflammatory responses by species-specific lactoferricin peptides

Alicia Malone, Rikki F. Clark, David W. Hoskin, Melanie R. Power Coombs

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

13 Citas (Scopus)

Resumen

Background: Inflammation is the body’s response to injury or infection and is important for healing and eliminating pathogens; however, prolonged inflammation is damaging and may lead to the development of chronic inflammatory disorders. Recently, there has been interest in exploiting antimicrobial peptides (AMPs) that exhibit immunoregulatory activities to treat inflammatory diseases. Methods: In this study, we investigated the immunomodulatory effects of lactoferrin-derived lactoferricin AMPs from three different species (bovine, mouse, and human) with subtle differences in their amino acid sequences that alter their antimicrobial action; to our knowledge, no other studies have compared their immunomodulatory effects. Macrophages, key players in the induction and propagation of inflammation, were used to investigate the effects of species-specific lactoferricin peptides on inflammatory processes. Results: Bovine lactoferricin was the only one of the three peptides studied that downregulated lipopolysaccharide (LPS)-induced pro-inflammatory cytokines, tumor necrosis factor (TNF)-α and interleukin (IL)-6, in both human and mouse macrophages. Lactoferricin regulated inflammation through targeting LPS-activated nuclear factor (NF)-κB and mitogen-activated protein kinase (MAPK) signaling pathways. Although the immunoregulatory role of lactoferricin during an inflammatory response in vivo is yet to be elucidated, further investigation with the use of animal models is warranted by the current findings. Conclusions: The ability of lactoferricin, especially that of bovine origin, to downregulate macrophage-mediated inflammatory responses suggests potential for the development of this peptide as a novel immunotherapeutic agent in the treatment of chronic inflammatory conditions.

Idioma originalEnglish
Número de artículo043
PublicaciónFrontiers in Bioscience - Landmark
Volumen27
N.º2
DOI
EstadoPublished - feb. 2022

Nota bibliográfica

Funding Information:
This research was funded by a NSERC Discovery Grant (D.H., RGPIN2017-05339)) and the Acadia University Research Fund (M.C.).

Publisher Copyright:
© 2022 The Author(s). Published by IMR Press.

ASJC Scopus Subject Areas

  • General Biochemistry,Genetics and Molecular Biology
  • General Immunology and Microbiology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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