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Xenophagic pathways and their bacterial subversion in cellular self-defense - παντα ρει - everything is in flux.
Radomski, Nadine; Rebbig, Annica; Leonhardt, Ralf M; Knittler, Michael R.
Afiliação
  • Radomski N; Institute of Immunology, Friedrich-Loeffler-Institut, Institute of Immunology, Federal Research Institute of Animal Health, D-17493 Greifswald, Isle of Riems, Germany.
  • Rebbig A; Institute of Immunology, Friedrich-Loeffler-Institut, Institute of Immunology, Federal Research Institute of Animal Health, D-17493 Greifswald, Isle of Riems, Germany.
  • Leonhardt RM; Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
  • Knittler MR; Institute of Immunology, Friedrich-Loeffler-Institut, Institute of Immunology, Federal Research Institute of Animal Health, D-17493 Greifswald, Isle of Riems, Germany. Electronic address: michael.knittler@fli.de.
Int J Med Microbiol ; 308(1): 185-196, 2018 Jan.
Article em En | MEDLINE | ID: mdl-29126745
ABSTRACT
Autophagy is an evolutionarily ancient and highly conserved eukaryotic mechanism that targets cytoplasmic material for degradation. Autophagic flux involves the formation of autophagosomes and their degradation by lysosomes. The process plays a crucial role in maintaining cellular homeostasis and responds to various environmental conditions. While autophagy had previously been thought to be a non-selective process, it is now clear that it can also selectively target cellular organelles, such as mitochondria (referred to as mitophagy) and/or invading pathogens (referred to as xenophagy). Selective autophagy is characterized by specific substrate recognition and requires distinct cellular adaptor proteins. Here we review xenophagic mechanisms involved in the recognition and autolysosomal or autophagolysosomal degradation of different intracellular bacteria. In this context, we also discuss a recently discovered cellular self-defense pathway, termed mito-xenophagy, which occurs during bacterial infection of dendritic cells and depends on a TNF-α-mediated metabolic switch from oxidative phosphorylation to glycolysis.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Bactérias / Autofagossomos / Lisossomos Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Bactérias / Autofagossomos / Lisossomos Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article