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1000 Titel
  • Id proteins: emerging roles in CNS disease and targets for modifying neural stemcell behavior
1000 Autor/in
  1. Chu, Yu-Hsuan |
  2. Lin, Jia-di |
  3. Nath, Suvra |
  4. Schachtrup, Christian |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-24
1000 Erschienen in
1000 Quellenangabe
  • 387(3):433-449
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00441-021-03490-z |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975794/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Neural stem/progenitor cells (NSPCs) are found in the adult brain and spinal cord, and endogenous or transplanted NSPCs contribute to repair processes and regulate immune responses in the CNS. However, the molecular mechanisms of NSPC survival and integration as well as their fate determination and functionality are still poorly understood. Inhibitor of DNA binding (Id) proteins are increasingly recognized as key determinants of NSPC fate specification. Id proteins act by antagonizing the DNA-binding activity of basic helix-loop-helix (bHLH) transcription factors, and the balance of Id and bHLH proteins determines cell fate decisions in numerous cell types and developmental stages. Id proteins are central in responses to environmental changes, as they occur in CNS injury and disease, and cellular responses in adult NSPCs implicate Id proteins as prime candidates for manipulating stemcell behavior. Here, we outline recent advances in understanding Id protein pleiotropic functions in CNS diseases and propose an integrated view of Id proteins and their promise as potential targets in modifying stemcell behavior to ameliorate CNS disease.
1000 Sacherschließung
lokal Multiple sclerosis
lokal Extracellular matrix
lokal Helix-loop-helix transcription factor
lokal Neural Stem Cells/metabolism [MeSH]
lokal Humans [MeSH]
lokal Small molecule inhibitors
lokal Review
lokal Fibrinogen
lokal Cell Differentiation/genetics [MeSH]
lokal Adult Stem Cells/metabolism [MeSH]
lokal Basic Helix-Loop-Helix Transcription Factors/metabolism [MeSH]
lokal Central Nervous System Diseases/therapy [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Q2h1LCBZdS1Ic3Vhbg==|https://frl.publisso.de/adhoc/uri/TGluLCBKaWEtZGk=|https://frl.publisso.de/adhoc/uri/TmF0aCwgU3V2cmE=|https://orcid.org/0000-0001-9851-6299
1000 Hinweis
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1000 Erstellt am 2023-04-28T14:04:31.071+0200
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1000 Zuletzt bearbeitet 2023-10-20T18:55:22.958+0200
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