4.7 Review

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

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 79, Issue 4, Pages -

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-022-04225-1

Keywords

Colony stimulating factor-1 receptor; Alzheimer's disease; Parkinson's disease; Huntington's disease; Amyotrophic lateral sclerosis; Multiple sclerosis

Funding

  1. Karolinska Institute
  2. Swedish Medical Research Council
  3. Neuroforbundet
  4. Alltid Lite Sterkere
  5. HjarnFonden
  6. AlzheimerFonden
  7. BarnCancerFonden
  8. Mayo Clinic Center for Regenerative Medicine
  9. Donald G. and Jodi P. Heeringa Family
  10. Haworth Family Professorship in Neurodegenerative Diseases Fund
  11. The Albertson Parkinson's Research Foundation
  12. NIH [R01NS091519, U54 HD090260, P30CA013330]

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This review article summarizes the recent advances in the use of CSF-1R inhibitors for treating neurodegenerative diseases and discusses potential challenges for clinical application.
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.

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