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Chitosan Polysaccharide Suppress Toll Like Receptor Dependent Immune Response
Date
2015-04-01
Author
Tincer, Gizem
Bayyurt Kocabaş, Banu
Arica, Yakup M.
Gursel, Ihsan
Metadata
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Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
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Chitosan is a widely used vaccine or anti-cancer delivery vehicle. In this study, we investigated the immunomodulatory effect of chitosan/pIC nanocomplexes on mouse immune cells. Materials and methods: Proliferative and cytotoxic features of chitosan were tested via CCK-8 assay on RAW 264.7. IL-1b p roduction was a ssessed v ia E LISA f rom PEC s upernatants. T NF-a, and NO induction from chitosan treated RAW cells detected by ELISA and Griess assay, respectively. mRNA message levels of TLRs and cytokines on macrophages in response to chitosan/pIC nanocomplex treatments were evaluated by RT-PCR. Results: Results revealed that chitosan is non-toxic to cells, however, proliferative capacities of macrophages were reduced by chitosan administration. Mouse PECs treated with chitosan, led to NLRP3 dependent inflammasome activation as evidenced by dose-dependent IL-1b secretion. Chitosan/pIC nanocomplexes did not improve immunostimulatory action of pIC on RAW cells, since TNF-a and NO productions remained unaltered. Expression levels of several TLRs, CXCL-16 and IFN-a messages from mouse splenocytes were down regulated in response to chitosan/pIC nanocomplex treatment. Conclusion: Our results revealed that chitosan is an anti-proliferative and inflammasome triggering macromolecule on immune cells. Utilization of chitosan as a carrier system is of concern for immunotherapeutic applications.
Subject Keywords
Biomaterial
,
chitosan
,
double-stranded ribonucleic acid
,
innate immunity
,
polysaccharide
,
Toll like receptor 3
,
DELIVERY
,
ACTIVATION
,
CHITIN
,
INFLAMMASOME
,
SYSTEMS
URI
https://hdl.handle.net/11511/96121
Journal
TURKISH JOURNAL OF IMMUNOLOGY
Collections
Department of Biology, Article
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G. Tincer, B. Bayyurt Kocabaş, Y. M. Arica, and I. Gursel, “Chitosan Polysaccharide Suppress Toll Like Receptor Dependent Immune Response,”
TURKISH JOURNAL OF IMMUNOLOGY
, vol. 3, no. 1, pp. 15–20, 2015, Accessed: 00, 2022. [Online]. Available: https://hdl.handle.net/11511/96121.