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Heme Oxygenase-1 Is an Anti-Inflammatory Host Factor that Promotes Murine Plasmodium Liver Infection

2008; Cell Press; Volume: 3; Issue: 5 Linguagem: Inglês

10.1016/j.chom.2008.04.003

1934-6069

Sabrina Epiphânio, Sebastian A. Mikolajczak, Lígia Antunes Gonçalves, Ana Pamplona, Sílvia Portugal, Sônia Sousa Melo Cavalcanti de Albuquerque, Michael S. Goldberg, Sofia Rebelo, Daniel G. Anderson, Akin Akinc, Hans‐Peter Vornlocher, Stefan H. I. Kappe, Miguel P. Soares, Maria M. Mota,

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The clinically silent Plasmodium liver stage is an obligatory step in the establishment of malaria infection and disease. We report here that expression of heme oxygenase-1 (HO-1, encoded by Hmox1) is upregulated in the liver following infection by Plasmodium berghei and Plasmodium yoelii sporozoites. HO-1 overexpression in the liver leads to a proportional increase in parasite liver load, and treatment of mice with carbon monoxide and with biliverdin, each an enzymatic product of HO-1, also increases parasite liver load. Conversely, mice lacking Hmox1 completely resolve the infection. In the absence of HO-1, the levels of inflammatory cytokines involved in the control of liver infection are increased. These findings suggest that, while stimulating inflammation, the liver stage of Plasmodium also induces HO-1 expression, which modulates the host inflammatory response, protecting the infected hepatocytes and promoting the liver stage of infection.