Characterization of Toll-like receptor-4 (TLR-4) in the spleen and thymus of Swiss albino mice and its modulation in experimental endotoxemia.

Abstract

Expression of innate immune receptors varies among organs and species and within different strains among the same species; thus, periodic classification of different pattern recognition receptors in the available strains is necessary to initiate different therapeutic approaches to combat inflammation. On characterization of TLR-4 in spleen and thymus of Swiss albino mice--with no reports of TLR-4 expression--induced with endotoxemia, it was found that the mode of expression varied among the organs at both mRNA and protein level in a time-dependent manner. Their functionality was verified by measuring proinflammatory and anti-inflammatory cytokines. In the in vitro study using isolated macrophages and lymphocytes from the same organs, the expression of TLR-4 after a shorter period of LPS stimulation was verified. The results substantiated the potent role of macrophage on LPS challenge compared to lymphocytes. The diverse pattern of TLR-4 expression on different cell population indicated their distinct functional activity in LPS-endotoxemia. It may be hypothesized that the expression patterns of TLR-4 could be different based on the anatomical localization and the varying bacterial milieu or bacterial endotoxin encountered in each anatomical location. Thus, blocking TLR-4 or administering IL-6 or IL-10 might impart protection against endotoxemia in the clinical field.

• Authors: Chandrayee Ghosh, Biswadev Bishayi
• Journal: Journal of immunology research (J Immunol Res) Vol. 2015 Pg. 137981 ( 2015) ISSN: 2314-7156 [Electronic] Egypt
• PMID: 25759837 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Culture Media, Conditioned
• Cytokines
• Inflammation Mediators
• Lipopolysaccharides
• RNA, Messenger
• Toll-Like Receptor 4
• C-Reactive Protein

Topics

• Animals
• C-Reactive Protein
• Culture Media, Conditioned (metabolism)
• Cytokines (blood)
• Disease Models, Animal
• Endotoxemia (genetics, immunology, metabolism, pathology)
• Gene Expression
• Immunomodulation
• Inflammation Mediators (blood)
• Lipopolysaccharides (immunology)
• Lymphocytes (immunology, metabolism)
• Macrophages (immunology, metabolism)
• Male
• Mice
• RNA, Messenger (genetics, metabolism)
• Spleen (immunology, metabolism, pathology)
• Thymus Gland (immunology, metabolism, pathology)
• Toll-Like Receptor 4 (genetics, metabolism)