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1000 Titel
  • Diversity of Reactive Astrogliosis in CNS Pathology: Heterogeneity or Plasticity?
1000 Autor/in
  1. Moulson, Aaron J. |
  2. Squair, Jordan W. |
  3. Franklin, Robin J. M. |
  4. Tetzlaff, Wolfram |
  5. Assinck, Peggy |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-26
1000 Erschienen in
1000 Quellenangabe
  • 15
1000 Copyrightjahr
  • 2021
1000 Embargo
  • 2022-01-28
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fncel.2021.703810 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349991/ |
1000 Publikationsstatus
1000 Abstract/Summary
  • Astrocytes are essential for the development and homeostatic maintenance of the central nervous system (CNS). They are also critical players in the CNS injury response during which they undergo a process referred to as 'reactive astrogliosis.' Diversity in astrocyte morphology and gene expression, as revealed by transcriptional analysis, is well-recognized and has been reported in several CNS pathologies, including ischemic stroke, CNS demyelination, and traumatic injury. This diversity appears unique to the specific pathology, with significant variance across temporal, topographical, age, and sex-specific variables. Despite this, there is limited functional data corroborating this diversity. Furthermore, as reactive astrocytes display significant environmental-dependent plasticity and fate-mapping data on astrocyte subsets in the adult CNS is limited, it remains unclear whether this diversity represents heterogeneity or plasticity. As astrocytes are important for neuronal survival and CNS function post-injury, establishing to what extent this diversity reflects distinct established heterogeneous astrocyte subpopulations vs. environmentally dependent plasticity within established astrocyte subsets will be critical for guiding therapeutic development. To that end, we review the current state of knowledge on astrocyte diversity in the context of three representative CNS pathologies: ischemic stroke, demyelination, and traumatic injury, with the goal of identifying key limitations in our current knowledge and suggesting future areas of research needed to address them. We suggest that the majority of identified astrocyte diversity in CNS pathologies to date represents plasticity in response to dynamically changing post-injury environments as opposed to heterogeneity, an important consideration for the understanding of disease pathogenesis and the development of therapeutic interventions.
1000 Sacherschließung
lokal spinal cord injury (SCI)
lokal Neuroscience
lokal ischemic stroke
lokal single-cell RNA sequencing
lokal reactive astrocytes
lokal traumatic brain injury (TBI)
lokal CNS demyelination
lokal plasticity
lokal heterogeneity
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TW91bHNvbiwgQWFyb24gSi4=|https://frl.publisso.de/adhoc/uri/U3F1YWlyLCBKb3JkYW4gVy4=|https://frl.publisso.de/adhoc/uri/RnJhbmtsaW4sIFJvYmluIEouIE0u|https://frl.publisso.de/adhoc/uri/VGV0emxhZmYsIFdvbGZyYW0=|https://frl.publisso.de/adhoc/uri/QXNzaW5jaywgUGVnZ3k=
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1000 Erstellt am 2024-04-11T11:33:33.011+0200
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1000 Objekt bearb. Tue May 07 13:26:23 CEST 2024
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