Cited by 275Neuroinflammation and Neurodegeneration MechanismsNeuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanisms

Questions and (some) answers on reactive astrocytes

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Escartin, Carole, Guillemaud, Océane, Carrillo‐de Sauvage, Maria‐Angeles·2019·Glia

Abstract

Astrocytes are key cellular partners for neurons in the central nervous system. Astrocytes react to virtually all types of pathological alterations in brain homeostasis by significant morphological and molecular changes. This response was classically viewed as stereotypical and is called astrogliosis or astrocyte reactivity. It was long considered as a nonspecific, secondary reaction to pathological conditions, offering no clues on disease‐causing mechanisms and with little therapeutic value. However, many studies over the last 30 years have underlined the crucial and active roles played by astrocytes in physiology, ranging from metabolic support, synapse maturation, and pruning to fine regulation of synaptic transmission. This prompted researchers to explore how these new astrocyte functions were changed in disease, and they reported alterations in many of them (sometimes beneficial, mostly deleterious). More recently, cell‐specific transcriptomics revealed that astrocytes undergo massive changes in gene expression when they become reactive. This observation further stressed that reactive astrocytes may be very different from normal, nonreactive astrocytes and could influence disease outcomes. To make the picture even more complex, both normal and reactive astrocytes were shown to be molecularly and functionally heterogeneous. Very little is known about the specific roles that each subtype of reactive astrocytes may play in different disease contexts. In this review, we have interrogated researchers in the field to identify and discuss points of consensus and controversies about reactive astrocytes, starting with their very name. We then present the emerging knowledge on these cells and future challenges in this field.

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  • The degree of GFAP upregulation in reactive astrocytes often parallels the severity of injury, but this correlation is not always proportional, perhaps due to regional differences of astrocytes including basal GFAP content.

    “However, while the degree of GFAP upregulation in reactive astrocytes often parallels the severity of the injury6, this correlation is not always proportional, perhaps due to regional differences of astrocytes, including basal GFAP content13,14.”

    From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [6]

    The passages available from our copy are repository metadata and navigation text, not the paper’s discussion; they have no section or page labels. Searches for GFAP upregulation, injury severity, regional differences, and basal GFAP content returned no passage addressing the claim, so it cannot be assessed from this copy. (LLM, conf=0.72)

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  • Responses of reactive astrocytes may be maladaptive and result in malfunctional astrocytes, which, in addition to losing homeostatic functions, may gain detrimental functions, thus exacerbating ongoing pathology.

    “Lastly, responses of reactive astrocytes may be maladaptive and result in malfunctional astrocytes, which, in addition to losing homeostatic functions, may also gain detrimental functions, thus exacerbating ongoing pathology6.”

    From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [6]

    The indexed passages are a HAL repository listing and site navigation, with no section or page of the paper’s substantive text. Searches for maladaptive responses, loss of homeostatic functions, detrimental functions, and worsening pathology returned no passage addressing the claim. (LLM, conf=0.72)

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References 217 · Cited by 275

Authors
Escartin, C., Guillemaud, O., & Carrillo‐de Sauvage, M.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Commissariat à l'Energie Atomique et aux Energies Alternatives, Département de la Recherche Fondamentale Institut de Biologie François Jacob, MIRCen Fontenay‐aux‐Roses France
Corresponding author
Escartin, Carole
Venue
Glia
Publisher
Wiley
Published
2019-08-19
Volume
67
Issue
12
Pages
2221-2247
ISSN
  • 0894-1491 (ISSN-L)
  • 1098-1136
OpenAlex
W2969998884
Cited by
275
References
217
Citations by year
2026: 16 · 2025: 16 · 2024: 41 · 2023: 47 · 2022: 50 · 2021: 67 · 2020: 30 · 2019: 6
FWCI
3.97
Type
journal article
Language
en
Open access
Locations
  • Glia (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
Funders
  • Agence Nationale de la Recherche (2010‐JCJC‐1402‐1, 2011‐BSV4‐021‐03, ANR‐16‐TERC‐00)
  • Centre National de la Recherche Scientifique
  • Commissariat à l'Énergie Atomique et aux Énergies Alternatives
  • Fondation Vaincre Alzheimer (FR‐15015)
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords
reactive astrocytes, astrocyte activation, astrocyte heterogeneity, astrocyte subtypes, astrocyte function, astrocyte gene expression, astrocyte-neuron interaction, brain homeostasis, neurodegenerative diseases
MeSH terms
Animals, Astrocytes, Brain, Central Nervous System Diseases, Gliosis, Humans

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