Th2-Associated Alternative Kupffer Cell Activation Promotes Liver Fibrosis without Inducing Local Inflammation


Por: López-Navarrete G., Ramos-Martínez E., Suárez-Álvarez K., Aguirre-García J., Ledezma-Soto Y., León-Cabrera S., Gudino-Zayas, M, Guzmán C., Gutiér-rez-Reyes G., Hernández-Ruíz J., Camacho-Arroyo I., Robles-Díaz G., Kershenobich D., Terrazas L.I., Escobedo G.

Publicada: 1 ene 2011
Resumen:
Cirrhosis is the final outcome of liver fibrosis. Kupffer cell-mediated hepatic inflammation is considered to aggravate liver injury and fibrosis. Alternatively-activated macrophages are able to control chronic inflammatory events and trigger wound healing processes. Nevertheless, the role of alternative Kupffer cell activation in liver harm is largely unclear. Thus, we evaluated the participation of alternatively-activated Kupffer cells during liver inflammation and fibrosis in the murine model of carbon tetrachloride-induced hepatic damage. To stimulate alternative activation in Kupffer cells, 20 Taenia crassiceps (Tc) larvae were inoculated into BALBc/AnN female mice. Six weeks post-inoculation, carbon tetrachloride or olive oil were orally administered to Tc-inoculated and non-inoculated mice twice per week during other six weeks. The initial exposure of animals to T. crassiceps resulted in high serum concentrations of IL-4 accompanied by a significant increase in the hepatic mRNA

Filiaciones:
López-Navarrete G.:
 Unidad de Medicina Experimental, Hospital General de México, Dr. Balmis #148, Col. Doc-tores, C.P. 06726, México D.F., Mexico

Ramos-Martínez E.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Dept Expt Med, Mexico City 06726, DF, Mexico

Suárez-Álvarez K.:
 Unidad de Medicina Experimental, Hospital General de México, Dr. Balmis #148, Col. Doc-tores, C.P. 06726, México D.F., Mexico

Aguirre-García J.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Unidad Patol, Mexico City 06726, DF, Mexico

Ledezma-Soto Y.:
 Univ Nacl Autonoma Mexico, Fac Estudios Super Iztacala, Unidad Biomed, Mexico City 54090, Estado De Mexic, Mexico

León-Cabrera S.:
 Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Mexico City 04510, DF, Mexico

Gudino-Zayas, M:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Dept Expt Med, Mexico City 06726, DF, Mexico

Guzmán C.:
 Unidad de Medicina Experimental, Hospital General de México, Dr. Balmis #148, Col. Doc-tores, C.P. 06726, México D.F., Mexico

Gutiér-rez-Reyes G.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Dept Expt Med, Mexico City 06726, DF, Mexico

Hernández-Ruíz J.:
 Unidad de Medicina Experimental, Hospital General de México, Dr. Balmis #148, Col. Doc-tores, C.P. 06726, México D.F., Mexico

Camacho-Arroyo I.:
 Univ Nacl Autonoma Mexico, Fac Quim, Dept Biol, Mexico City 04510, DF, Mexico

Robles-Díaz G.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Dept Expt Med, Mexico City 06726, DF, Mexico

Kershenobich D.:
 Univ Nacl Autonoma Mexico, Hosp Gen Mexico, Fac Med, Dept Expt Med, Mexico City 06726, DF, Mexico

Terrazas L.I.:
 Univ Nacl Autonoma Mexico, Fac Estudios Super Iztacala, Unidad Biomed, Mexico City 54090, Estado De Mexic, Mexico

Escobedo G.:
 Unidad de Medicina Experimental, Hospital General de México, Dr. Balmis #148, Col. Doc-tores, C.P. 06726, México D.F., Mexico
ISSN: 14492288
Editorial
IVYSPRING INT PUBL, PO BOX 4546, LAKE HAVEN, NSW 2263, AUSTRALIA, Australia
Tipo de documento: Article
Volumen: 7 Número: 9
Páginas: 1273-1286
WOS Id: 000298011000006
ID de PubMed: 22110380
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