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Autophagy. 2021 Jun;17(6):1448-1457. doi: 10.1080/15548627.2020.1765521. Epub 2020 Jun 19.

Neutrophils use selective autophagy receptor Sqstm1/p62 to target .

Autophagy

Josie F Gibson, Tomasz K Prajsnar, Christopher J Hill, Amy K Tooke, Justyna J Serba, Rebecca D Tonge, Simon J Foster, Andrew J Grierson, Philip W Ingham, Stephen A Renshaw, Simon A Johnston

Affiliations

  1. Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, Sheffield, UK.
  2. The Bateson Centre, University of Sheffield, Sheffield, UK.
  3. Institute of Molecular and Cell Biology, Agency of Science, Technology and Research (A-star), Singapore.
  4. Florey Institute, University of Sheffield, Sheffield, UK.
  5. Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield, UK.
  6. Institute Biology Leiden, Leiden University, Leiden, The Netherlands.
  7. Sheffield Institute for Translational Neuroscience, Department of Neuroscience, University of Sheffield, Sheffield, UK.
  8. Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.

PMID: 32559122 PMCID: PMC8204994 DOI: 10.1080/15548627.2020.1765521

Abstract

Macroautophagy/autophagy functions to degrade cellular components and intracellular pathogens. Autophagy receptors, including SQSTM1/p62, target intracellular pathogens.

Keywords: Autophagy; bacterial infection; host-pathogen interactions; neutrophil; sqstm1/p62; staphylococcus aureus; xenophagy; zebrafish

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