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HGF Secreted by Activated Kupffer Cells Induces Apoptosis of Plasmodium-Infected Hepatocytes

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Gonçalves_Front.Immunol.2017_pdfmain article3.67 MBAdobe PDF Ver/Abrir
es_Front.Immunol.2017_SM_.pdfsupplementary material60.42 KBAdobe PDF Ver/Abrir

Orientador(es)

Resumo(s)

Malaria liver stage infection is an obligatory parasite development step and represents a population bottleneck in Plasmodium infections, providing an advantageous target for blocking parasite cycle progression. Parasite development inside hepatocytes implies a gross cellular insult evoking innate host responses to counteract intra-hepatocytic infection. Using primary hepatocyte cultures, we investigated the role of Kupffer cell-derived hepatocyte growth factor (HGF) in malaria liver stage infection. We found that Kupffer cells from Plasmodium-infected livers produced high levels of HGF, which trigger apoptosis of infected hepatocytes through a mitochondrial-independent apoptosis pathway. HGF action in infected hepatocyte primary cultures results in a potent reduction of parasite yield by specifically sensitizing hepatocytes carrying established parasite exo-erythrocytic forms to undergo apoptosis. This apoptosis mechanism is distinct from cell death that is spontaneously induced in infected cultures and is governed by Fas signaling modulation through a mitochondrial-dependent apoptosis pathway. This work indicates that HGF and Fas signaling pathways are part of an orchestrated host apoptosis response that occurs during malaria liver stage infection, decreasing the success of infection of individual hepatocytes. Our results raise the hypothesis that paracrine signals derived from Kupffer cell activation are implicated in directing death of hepatocytes infected with the malaria parasite.

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Palavras-chave

Plasmodium Kupffer cells hepatocytes HGF apoptosis malaria liver

Contexto Educativo

Citação

Gonçalves LA, Rodo J, Rodrigues- Duarte L, de Moraes LV and Penha-Gonçalves C (2017) HGF Secreted by Activated Kupffer Cells Induces Apoptosis of Plasmodium- Infected Hepatocytes. Front. Immunol. 8:90. doi: 10.3389/fimmu.2017.00090

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Fascículo

Editora

Frontiers Media

Licença CC

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