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Targeting Autophagy, Oxidative Stress, and Er Stress for Neurodegenerative Disease Treatment Publisher Pubmed



Esmaeili Y1 ; Yarjanli Z2 ; Pakniya F3 ; Bidram E1 ; Los MJ4 ; Eshraghi M5 ; Klionsky DJ6 ; Ghavami S5, 7, 8 ; Zarrabi A9
Authors
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Authors Affiliations
  1. 1. Biosensor Research Center, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  3. 3. Department of Biotechnology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran
  4. 4. Biotechnology Center, Silesian University of Technology, 8 Krzywousty St., Gliwice, 44-100, Poland
  5. 5. Department of Human Anatomy and Cell Science, Rady Faculty of Health Sciences, Max Rady College of Medicine, University of Manitoba, Winnipeg, R3E 0J9, MB, Canada
  6. 6. Life Sciences Institute, University of Michigan, Ann Arbor, MI, United States
  7. 7. Faculty of Medicine, Katowice School of Technology, ul. Rolna 43, Katowice, 40-555, Poland
  8. 8. Research Institute of Oncology and Hematology, Cancer Care Manitoba, University of Manitoba, Winnipeg, R3E 0V9, MB, Canada
  9. 9. Department of Biomedical Engineering, Faculty of Engineering and Natural Sciences, Istinye University, Sariyer, Istanbul, 34396, Turkey

Source: Journal of Controlled Release Published:2022


Abstract

Protein homeostasis is a vital process for cell function and, therefore, disruption of the molecular mechanisms involved in this process, such as autophagy, may contribute to neurodegenerative diseases (NDs). Apart from autophagy disruption, excess oxidative stress and endoplasmic reticulum (ER) stress are additional main molecular mechanisms underlying neurodegeneration, leading to protein aggregation, and mitochondrial dysfunction. Notably, these primary molecular processes are interconnected pathways, which have synergistic effects on each other. Therefore, we propose that targeting of the crosstalk between autophagy, oxidative stress and ER stress simultaneously may play a critical role in healing NDs. NeuroNanoTechnology, as a revolutionized approach, in combination with an in-silico strategy, holds great promise for developing de-novo structures for targeting and modulating neuro-molecular pathways. Accordingly, this review outlines the contributions of autophagy, oxidative stress, and ER stress in neurodegenerative conditions along with a particular focus on the crosstalk among these pathways. Furthermore, we provide a comprehensive discussion on the potential of nanomaterials to target this crosstalk and suggest this potential as a promising opportunity in neuroprotection. © 2022
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