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Necrotic, Apoptotic and Autophagic Cell Fates Triggered by Nanoparticles Publisher Pubmed



Mohammadinejad R1 ; Moosavi MA2 ; Tavakol S3 ; Vardar DO4 ; Hosseini A5 ; Rahmati M6 ; Dini L7 ; Hussain S8 ; Mandegary A9 ; Klionsky DJ10
Authors
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Authors Affiliations
  1. 1. Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
  2. 2. Department of Molecular Medicine, Institute of Medical Biotechnology, National Institute for Genetic Engineering and Biotechnology, Tehran, Iran
  3. 3. Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Sungurlu Vocational High School, Health Programs, Hitit University, Corum, Turkey
  5. 5. Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
  6. 6. Cancer Biology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. CNR Nanotec, Lecce, Italy
  8. 8. Department of Physiology, Pharmacology and Neuroscience, West Virginia University, School of Medicine, Morgantown, WV, United States
  9. 9. Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
  10. 10. Life Sciences Institute, University of Michigan, Ann Arbor, MI, United States

Source: Autophagy Published:2019


Abstract

Nanomaterials have gained a rapid increase in use in a variety of applications that pertain to many aspects of human life. The majority of these innovations are centered on medical applications and a range of industrial and environmental uses ranging from electronics to environmental remediation. Despite the advantages of NPs, the knowledge of their toxicological behavior and their interactions with the cellular machinery that determines cell fate is extremely limited. This review is an attempt to summarize and increase our understanding of the mechanistic basis of nanomaterial interactions with the cellular machinery that governs cell fate and activity. We review the mechanisms of NP-induced necrosis, apoptosis and autophagy and potential implications of these pathways in nanomaterial-induced outcomes. Abbreviations: Ag, silver; CdTe, cadmium telluride; CNTs, carbon nanotubes; EC, endothelial cell; GFP, green fluorescent protein; GO, graphene oxide; GSH, glutathione; HUVECs, human umbilical vein endothelial cells; NP, nanoparticle; PEI, polyethylenimine; PVP, polyvinylpyrrolidone; QD, quantum dot; ROS, reactive oxygen species; SiO2, silicon dioxide; SPIONs, superparamagnetic iron oxide nanoparticles; SWCNT, single-walled carbon nanotubes; TiO2, titanium dioxide; USPION, ultra-small super paramagnetic iron oxide; ZnO, zinc oxide. © 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
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