Importance of TLR2 on hepatic immune and non-immune cells to attenuate the strong inflammatory liver response during Trypanosoma cruzi acute infection.

BACKGROUND: Toll-like receptors (TLR) and cytokines play a central role in the pathogen clearance as well as in pathological processes. Recently, we reported that TLR2, TLR4 and TLR9 are differentially modulated in injured livers from BALB/c and C57BL/6 (B6) mice during Trypanosoma cruzi infection....

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Main Authors: Eugenio Antonio Carrera-Silva (Author), Natalia Guiñazu (Author), Andrea Pellegrini (Author), Roxana Carolina Cano (Author), Alfredo Arocena (Author), Maria Pilar Aoki (Author), Susana Gea (Author)
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Published: Public Library of Science (PLoS), 2010-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Eugenio Antonio Carrera-Silva  |e author 
700 1 0 |a Natalia Guiñazu  |e author 
700 1 0 |a Andrea Pellegrini  |e author 
700 1 0 |a Roxana Carolina Cano  |e author 
700 1 0 |a Alfredo Arocena  |e author 
700 1 0 |a Maria Pilar Aoki  |e author 
700 1 0 |a Susana Gea  |e author 
245 0 0 |a Importance of TLR2 on hepatic immune and non-immune cells to attenuate the strong inflammatory liver response during Trypanosoma cruzi acute infection. 
260 |b Public Library of Science (PLoS),   |c 2010-01-01T00:00:00Z. 
500 |a 1935-2735 
500 |a 10.1371/journal.pntd.0000863 
520 |a BACKGROUND: Toll-like receptors (TLR) and cytokines play a central role in the pathogen clearance as well as in pathological processes. Recently, we reported that TLR2, TLR4 and TLR9 are differentially modulated in injured livers from BALB/c and C57BL/6 (B6) mice during Trypanosoma cruzi infection. However, the molecular and cellular mechanisms involved in local immune response remain unclear. METHODOLOGY/PRINCIPAL FINDINGS: In this study, we demonstrate that hepatic leukocytes from infected B6 mice produced higher amounts of pro-inflammatory cytokines than BALB/c mice, whereas IL10 and TGFβ were only released by hepatic leukocytes from BALB/c. Strikingly, a higher expression of TLR2 and TLR4 was observed in hepatocytes of infected BALB/c mice. However, in infected B6 mice, the strong pro-inflammatory response was associated with a high and sustained expression of TLR9 and iNOS in leukocytes and hepatic tissue respectively. Additionally, co-expression of gp91- and p47-phox NADPH oxidase subunits were detected in liver tissue of infected B6 mice. Notably, the pre-treatment previous to infection with Pam3CSK4, TLR2-agonist, induced a significant reduction of transaminase activity levels and inflammatory foci number in livers of infected B6 mice. Moreover, lower pro-inflammatory cytokines and increased TGFβ levels were detected in purified hepatic leukocytes from TLR2-agonist pre-treated B6 mice. CONCLUSIONS/SIGNIFICANCE: Our results describe some of the main injurious signals involved in liver immune response during the T. cruzi acute infection. Additionally we show that the administration of Pam3CSk4, previous to infection, can attenuate the exacerbated inflammatory response of livers in B6 mice. These results could be useful to understand and design novel immune strategies in controlling liver pathologies. 
546 |a EN 
690 |a Arctic medicine. Tropical medicine 
690 |a RC955-962 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n PLoS Neglected Tropical Diseases, Vol 4, Iss 11, p e863 (2010) 
787 0 |n http://europepmc.org/articles/PMC2970533?pdf=render 
787 0 |n https://doaj.org/toc/1935-2735 
856 4 1 |u https://doaj.org/article/1cb46684468c44d4864f8b9d25a076c9  |z Connect to this object online.