Local and remote tissue injury upon intestinal ischemia and reperfusion depends on the TLR/MyD88 signaling pathway


Autoria(s): VICTONI, Tatiana; COELHO, Fernando Rodrigues; SOARES, Alexandre Learth; FREITAS, Andressa de; SECHER, Thomas; GUABIRABA, Rodrigo; ERARD, Francois; OLIVEIRA-FILHO, Ricardo Martins de; VARGAFTIG, B. Boris; LAUVAUX, Gregoire; KAMAL, Mamdouh A.; RYFFEL, Bernhard; MOSER, Rene; TAVARES-DE-LIMA, Wothan
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Innate immune responses against microorganisms may be mediated by Toll-like receptors (TLRs). Intestinal ischemia-reperfusion (i-I/R) leads to the translocation of bacteria and/or bacterial products such as endotoxin, which activate TLRs leading to acute intestinal and lung injury and inflammation observed upon gut trauma. Here, we investigated the role of TLR activation by using mice deficient for the common TLR adaptor protein myeloid differentiation factor 88 (MyD88) on local and remote inflammation following intestinal ischemia. Balb/c and MyD88(-/-) mice were subjected to occlusion of the superior mesenteric artery (45 min) followed by intestinal reperfusion (4 h). Acute neutrophil recruitment into the intestinal wall and the lung was significantly diminished in MyD88(-/-) after i-I/R, which was confirmed microscopically. Diminished neutrophil recruitment was accompanied with reduced concentration of TNF-alpha and IL-1 beta level. Furthermore, diminished microvascular leak and bacteremia were associated with enhanced survival of MyD88(-/-) mice. However, neither TNF-alpha nor IL-1 beta neutralization prevented neutrophil recruitment into the lung but attenuated intestinal inflammation upon i-I/R. In conclusion, our data demonstrate that disruption of the TLR/MyD88 pathway in mice attenuates acute intestinal and lung injury, inflammation, and endothelial damage allowing enhanced survival.

Fondation pour la Recherche Medicale

Fondation pour la Recherche Medicale

European Community

European Community, EC[ndegree 028190]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[02/06606-3]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[04/14128-0]

Conselho Nacional de Pesquisa (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

MEDICAL MICROBIOLOGY AND IMMUNOLOGY, v.199, n.1, p.35-42, 2010

0300-8584

http://producao.usp.br/handle/BDPI/28175

10.1007/s00430-009-0134-5

http://dx.doi.org/10.1007/s00430-009-0134-5

Idioma(s)

eng

Publicador

SPRINGER

Relação

Medical Microbiology and Immunology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Intestinal ischemia #MyD88 #TLR #Lung inflammation #LUNG INJURY #TNF-ALPHA #ISCHEMIA/REPERFUSION INJURY #NEUTROPHIL SEQUESTRATION #AIRWAY RESPONSE #NITRIC-OXIDE #ENDOTOXIN #MICE #PERMEABILITY #RATS #Immunology #Microbiology
Tipo

article

original article

publishedVersion