中国神经再生研究(英文版) ›› 2024, Vol. 19 ›› Issue (3): 505-506.doi: 10.4103/1673-5374.377609

• 观点:神经损伤修复保护与再生 • 上一篇    下一篇

神经元对星形胶质细胞的应激信号应答

  

  • 出版日期:2024-03-15 发布日期:2023-09-02

Neuron-to-astrocyte proteostatic stress signaling in response to tau pathology

Kevin Llewelyn Batenburg, Wiep Scheper*#br#   

  1. Amsterdam UMC location Vrije Universiteit Amsterdam, Department of Human Genetics, Amsterdam Neuroscience - Neurodegeneration, Amsterdam, The Netherlands (Batenburg KL, Scheper W)
    Department of Functional Genomics, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, Amsterdam Neuroscience - Neurodegeneration, Amsterdam, The Netherlands (Batenburg KL, Scheper W)
  • Online:2024-03-15 Published:2023-09-02
  • Contact: Wiep Scheper, PhD, w.scheper@amsterdamumc.nl.
  • Supported by:
    The experimental work from our group described in this perspective was supported by ZonMW and Stichting Proefdiervrij (#114022506), PPP Allowance made available by Health~Holland, Top Sector Life Sciences & Health, to stimulate public-private partnerships (#LSHM17014 and LSHM18024), Alzheimer Nederland (grant WE.03-2017-10), European Commission (Joint Programming Initiative Neurodegenerative Diseases/JPco-fuND (ZonMW #733051062), Weston Brain Institute (#NR160014) and ZonMW Memorabel/Alzheimer Nederland (#733050101) (to WS).

摘要: https://orcid.org/0000-0002-1431-4559 (Wiep Scheper)

Abstract: Maintenance of protein homeostasis or “proteostasis” is essential for the functioning and viability of cells. This is in particular the case for cells like neurons that cannot self-renew and acquire unique functional properties during their lifetime. Cellular proteostatic stress responses are in place to protect cells from damage in case of proteostatic challenges. The integrated stress response (ISR) is one of the key proteostatic stress responses in the cell (Costa-Mattioli and Walter, 2020). The ISR is the downstream convergence point for the four stress-induced eIF2α kinases (EIF2AK1–4) that control stress-regulated protein translation via phosphorylation of the translation factor eIF2α. ISR activation results in a transient reduction of global translation while it concomitantly enhances the translation of specific mRNAs, including that encoding the activating transcription factor 4 (ATF4). Together, the translational control mediated by the ISR results in a temporary reduction of the overall protein load and the selectively increased expression of proteins that contribute to restoration of the proteostatic balance.