Toll-like receptor 2 and 4 ligation results in complex altered cytokine profiles early and late after burn injury

作者：Cairns Bruce A^*; Barnes Carie M; Mlot Stqfan; Meyer Anthony A; Maile Robert

来源：Journal of Trauma-Injury Infection and Critical Care, 2008, 64(4): 1069-1077.

DOI：10.1097/TA.0b013e318166b7d9

• burn injury
• toll-like receptors
• cytokines
• macrophages
• cell death

Background: Toll-like receptors (TLR) 2 and TLR4 expressed on innate immune cells are important mediators of the immune response to pathogens. In this study, we hypothesized that burn injury results in altered cytokine secretion profiles after TLR2 or TLR4 ligation that is associated with altered TLR expression on innate immune cells.
Methods: Female C56BL/6 mice were subjected to 20% full thickness burn or sham injury. Three or 14 days after injury whole splenocytes or purified splenic macrophages were cultured with TLR2 ligand peptidoglycan or TLR4 ligand lipopolysaccharide. Supernatants were assayed for TNF-alpha, MCP-1, IL-6 and IL-10. Cell death was assessed using flow cytometry. Innate CD11b(+) F4/80(+) macrophages were sorted 14 days after burn injury and TLR2 and 4 expression was determined by quantitative reverse-transcriptase polymerase chain reaction and now cytometry.
Results: Burn injury results in a steady accumulation in the periphery of CD11b(+)F4/80(+) macrophages. Macrophages purified early after burn injury upregulated TLR2 and 4, followed by a decrease of TLR2 and TLR4 expression late after burn injury. TLR2 and TLR4 ligation of an equivalent number of purified macrophages 3 days after burn injury revealed no significant differences in cytokine secretion compared with sham. Stimulation 14 days after burn injury revealed a significant reduction in tumor necrosis factor-a secretion by macrophages compared with sham mice. In contrast, interleukin-10 was significantly increased (mean, similar to 1.8-fold) late after burn injury after either TLR2 or TLR4 stimulation. Interleukin-6 and monocyte chemotactic protein-1 secretion was unchanged from sham levels. In contrast, whole splenocyte stimulation resulted in increased cytokine 3 days and 14 days after burn injury. This effect is likely caused by the accumulation of TLRlow macrophages, which are resistant to TLR-induced cell death.
Conclusions: Cytokine secretion profiles after TLR2 and TLR4 ligation after burn injury are altered in a manner not clearly reflective of an anti-inflammatory or proinflammatory state and are associated with unique changes in the macrophage population. TLR2 and TLR4 ligation have complex and varied roles in mediating the immune response to burn injury.

• 出版日期2008-4