Adamantane Containing Peptidoglycan Fragments Enhance RANTES and IL-6 Production in Lipopolysaccharide-Induced Macrophages

• Published in: Molecules (Basel, Switzerland) Switzerland), 2020-08, Vol.25 (16), p.3707
• Main Authors: Manček-Keber, Mateja, Ribić, Rosana, Chain, Fernando, Sinnaeve, Davy, Martins, José C, Jerala, Roman, Tomić, Srđanka, Fehér, Krisztina
• Format: Article
• Language: English
• Subjects: adamantane; Adamantane - chemistry; Animals; Bone marrow; Cell activation; Cells, Cultured; Chemokine CCL5 - metabolism; Chemokines; Chirality; Communication; Cytokines; Fragments; Immune response; Immune system; Immunology; immunostimulation; Influence; Innate immunity; Interleukin 6; Interleukin-6 - metabolism; Investigations; Life Sciences; Lipid bilayers; lipid incapsulation; Lipids; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Lymphocytes; Lymphocytes T; Macrophages; Macrophages - drug effects; Macrophages - immunology; Macrophages - metabolism; Mannose; Mannose receptors; Mice; Mice, Inbred C57BL; Nanoparticles; peptidoglycan; Peptidoglycan - chemistry; Peptidoglycan - pharmacology; Peptidoglycans; Proteins; RANTES; Tumor necrosis factor-TNF; Vaccinology
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules25163707

We report the enhancement of the lipopolysaccharide-induced immune response by adamantane containing peptidoglycan fragments in vitro. The immune stimulation was detected by Il-6 (interleukine 6) and RANTES (regulated on activation, normal T cell expressed and secreted) chemokine expression using cell assays on immortalized mouse bone-marrow derived macrophages. The most active compound was a α-D-mannosyl derivative of an adamantylated tripeptide with L-chirality at the adamantyl group attachment, whereby the mannose moiety assumed to target mannose receptors expressed on macrophage cell surfaces. The immune co-stimulatory effect was also influenced by the configuration of the adamantyl center, revealing the importance of specific molecular recognition event taking place with its receptor. The immunostimulating activities of these compounds were further enhanced upon their incorporation into lipid bilayers, which is likely related to the presence of the adamantyl group that helps anchor the peptidoglycan fragment into lipid nanoparticles. We concluded that the proposed adamantane containing peptidoglycan fragments act as co-stimulatory agents and are also suitable for the preparation of lipid nanoparticle-based delivery of peptidoglycan fragments.