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  • Han, JM (author)

Inhibition of colony stimulating factor-1 receptor (CSF-1R) as a potential therapeutic strategy for neurodegenerative diseases: opportunities and challenges

  • Article/chapterEnglish2022

Publisher, publication year, extent ...

  • 2022-04-02
  • Springer Science and Business Media LLC,2022

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:149259241
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:149259241URI
  • https://doi.org/10.1007/s00018-022-04225-1DOI

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  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Microglia are specialized dynamic immune cells in the central nervous system (CNS) that plays a crucial role in brain homeostasis and in disease states. Persistent neuroinflammation is considered a hallmark of many neurodegenerative diseases, including Alzheimer’s disease (AD), Parkinson's disease (PD), Huntington’s disease (HD), amyotrophic lateral sclerosis (ALS) and primary progressive multiple sclerosis (MS). Colony stimulating factor 1-receptor (CSF-1R) is predominantly expressed on microglia and its expression is significantly increased in neurodegenerative diseases. Cumulative findings have indicated that CSF-1R inhibitors can have beneficial effects in preclinical neurodegenerative disease models. Research using CSF-1R inhibitors has now been extended into non-human primates and humans. This review article summarizes the most recent advances using CSF-1R inhibitors in different neurodegenerative conditions including AD, PD, HD, ALS and MS. Potential challenges for translating these findings into clinical practice are presented.

Added entries (persons, corporate bodies, meetings, titles ...)

  • Chitu, V (author)
  • Stanley, ER (author)
  • Wszolek, ZK (author)
  • Karrenbauer, VDKarolinska Institutet (author)
  • Harris, RAKarolinska Institutet (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Cellular and molecular life sciences : CMLS: Springer Science and Business Media LLC79:4, s. 219-1420-90711420-682X

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