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Small heat shock proteins in neurodegenerative diseases

期刊

CELL STRESS & CHAPERONES
卷 25, 期 4, 页码 679-699

出版社

SPRINGER
DOI: 10.1007/s12192-020-01101-4

关键词

Small heat shock proteins; Hereditary peripheral neuropathies; Diseases of the central nervous system; Neurodegeneration; Protein aggregation

资金

  1. Flanders Fund for Scientific Research (FWO)
  2. FWO research grant [G041416N]
  3. Rotary Hope in Head program
  4. American Muscular Dystrophy Association (MDA) [577497]
  5. Association Francaise contre les Myopathies (AFM) [21533]
  6. Association Belge contre les Maladies Neuromusculaires (ABMM)
  7. Medical Foundation Queen Elisabeth (GSKE)
  8. EC 7th Framework Programme NEUROMICS, Integrated Europeanomics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases [2012-305121]
  9. H2020 grant Solve-RD programme Solving the unsolved rare diseases [2017-779257]

向作者/读者索取更多资源

Small heat shock proteins are ubiquitously expressed chaperones, yet mutations in some of them cause tissue-specific diseases. Here, we will discuss how small heat shock proteins give rise to neurodegenerative disorders themselves while we will also highlight how these proteins can fulfil protective functions in neurodegenerative disorders caused by protein aggregation. The first half of this paper will be focused on how mutations in HSPB1, HSPB3, and HSPB8 are linked to inherited peripheral neuropathies like Charcot-Marie-Tooth (CMT) disease and distal hereditary motor neuropathy (dHMN). The second part of the paper will discuss how small heat shock proteins are linked to neurodegenerative disorders like Alzheimer's, Parkinson's, and Huntington's disease.

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