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Mitochondrial Reactive Oxygen Species Participate in Signaling Triggered by Heme in Macrophages and upon Hemolysis

Prestes, Elisa B ; Alves, Letícia S ; Rodrigues, Danielle A S ; Dutra, Fabianno F ; Fernandez, Patricia L ; Paiva, Claudia N ; Kagan, Jonathan C ; Bozza, Marcelo T

The Journal of immunology (1950), 2020-11, Vol.205 (10), p.2795-2805 [Periódico revisado por pares]

United States

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Título:
Mitochondrial Reactive Oxygen Species Participate in Signaling Triggered by Heme in Macrophages and upon Hemolysis
Autor: Prestes, Elisa B ; Alves, Letícia S ; Rodrigues, Danielle A S ; Dutra, Fabianno F ; Fernandez, Patricia L ; Paiva, Claudia N ; Kagan, Jonathan C ; Bozza, Marcelo T
Assuntos: Animals ; Chemokine CXCL1 - metabolism ; Disease Models, Animal ; Heme - metabolism ; Hemolysis - immunology ; Humans ; Macrophages - cytology ; Macrophages - immunology ; Mice ; Mice, Knockout ; Mitochondria - immunology ; Mitochondria - metabolism ; Mitogen-Activated Protein Kinase 1 - metabolism ; Mitogen-Activated Protein Kinase 3 - metabolism ; Phosphorylation - immunology ; Reactive Oxygen Species - metabolism ; Receptors, Tumor Necrosis Factor, Type I - genetics ; Receptors, Tumor Necrosis Factor, Type I - metabolism ; Signal Transduction - immunology ; Syk Kinase - metabolism ; Toll-Like Receptor 4 - genetics ; Toll-Like Receptor 4 - metabolism ; Tumor Necrosis Factor-alpha - metabolism
É parte de: The Journal of immunology (1950), 2020-11, Vol.205 (10), p.2795-2805
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
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Descrição: Hemolysis causes an increase of intravascular heme, oxidative damage, and inflammation in which macrophages play a critical role. In these cells, heme can act as a prototypical damage-associated molecular pattern, inducing TLR4-dependent cytokine production through the MyD88 pathway, independently of TRIF. Heme promotes reactive oxygen species (ROS) generation independently of TLR4. ROS and TNF production contribute to heme-induced necroptosis and inflammasome activation; however, the role of ROS in proinflammatory signaling and cytokine production remains unknown. In this study, we demonstrate that heme activates at least three signaling pathways that contribute to a robust MAPK phosphorylation and cytokine expression in mouse macrophages. Although heme did not induce a detectable Myddosome formation, the TLR4/MyD88 axis was important for phosphorylation of p38 and secretion of cytokines. ROS generation and spleen tyrosine kinase (Syk) activation induced by heme were critical for most proinflammatory signaling pathways, as the antioxidant -acetyl-l-cysteine and a Syk inhibitor differentially blocked heme-induced ROS, MAPK phosphorylation, and cytokine production in macrophages. Early generated mitochondrial ROS induced by heme was Syk dependent, selectively promoted the phosphorylation of ERK1/2 without affecting JNK or p38, and contributed to CXCL1 and TNF production. Finally, lethality caused by sterile hemolysis in mice required TLR4, TNFR1, and mitochondrial ROS, supporting the rationale to target these pathways to mitigate tissue damage of hemolytic disorders.
Editor: United States
Idioma: Inglês

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Mitochondrial Reactive Oxygen Species Participate in Signaling Triggered by Heme in Macrophages and upon Hemolysis

Prestes, Elisa B ; Alves, Letícia S ; Rodrigues, Danielle A S ; Dutra, Fabianno F ; Fernandez, Patricia L ; Paiva, Claudia N ; Kagan, Jonathan C ; Bozza, Marcelo T

United States

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