Astrocyte morphology: Diversity, plasticity, and role in neurological diseases
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Summary: Astrocytes are the most abundant glial cells in the central nervous system (CNS) and participate in synaptic, circuit, and behavioral functions. The well‐developed protoplasmic astrocytes contain numerous processes forming well‐delineated bushy territories that overlap by as little as 5% at their boundaries. This highly complex morphology, with up to approximately 80% of the cell's membrane constituted by fine processes with dimensions on the tens of nanometer scale and high surface area to volume ratios, comes in contact with synapses, blood vessels, and other glial cells. Recent progress is challenging the conventional view that astrocytes are morphologically homogeneous throughout the brain; instead, they display circuit‐ and region‐specific morphological diversity that may contribute to the heterogeneous astrocyte‐neuron spatiotemporal interplay in different brain areas. Further, the fine structure of astrocytes is found to be highly plastic and activity‐dependent. We are beginning to understand how astrocyte structural plasticity contributes to brain functions. The change/loss of astrocyte morphology, traditionally known as a hallmark for reactive astrogliosis, is a common pathological feature in many neurological disorders. However, recent data suggest the fine structural deficits preceding reactive astrogliosis may drive disease progression. This review summarizes recent advances in astrocyte morphological diversity, plasticity, and disease‐related deficits.
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Under pathological conditions, astrocytes undergo reactive astrogliosis characterized by morphological and functional changes such as hypertrophy, process elongation, up-regulation of GFAP, or dynamic relocalization of proteins such as aquaporin-4.
“Under pathological conditions, they undergo reactive astrogliosis, characterized by morphological and functional changes such as hypertrophy, process elongation, up-regulation of glial fibrillary acidic protein (GFAP) (2–5), or dynamic relocalization of proteins such as aquaporin-4 (6, 7).”
From Varicose projection astrocytes: Conserved reactive cells in brain pathology (2026) · cites this paper as [2]
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Varicose projection astrocytes: Conserved reactive cells in brain pathology
Ciani, C., Pistorio, G., Giancola, S., Mearelli, M., Mongelli, F. E., Forouzeh, D., Campos Soares, L., Gonzalez Martin, M., Lichtenstein, M. E., Mio, L., et al. (2026) · Science Advances · doi:10.1126/sciadv.ady8204 · Cited by 4 · see citing works
- Authors
- Zhou, B., Zuo, Y., & Jiang, R.
- Affiliations
- Sichuan University (CN)
- Laboratory of Anesthesia and Critical Care Medicine, Department of Anesthesiology, Translational Neuroscience Center West China Hospital, Sichuan University Chengdu China
- Venue
- CNS Neuroscience & Therapeutics
- Publisher
- Wiley
- Published
- 2019-03-30
- Volume
- 25
- Issue
- 6
- Pages
- 665-673
- ISSN
- 1755-5930 (ISSN-L)
- 1755-5949
- PMC
- PMC6515705
- OpenAlex
- W2925613754
- Cited by
- 417
- References
- 9
- Citations by year
- 2026: 44 · 2025: 89 · 2024: 87 · 2023: 80 · 2022: 63 · 2021: 33 · 2020: 13 · 2019: 8
- FWCI
- 3.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- CNS Neuroscience & Therapeutics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Thousand Talents Plan in Sichuan Province
- The National Natural Science Foundation of China (31600832, 8187051920)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- astrocyte morphology, protoplasmic astrocyte, astrocyte heterogeneity, astrocyte-neuron interaction, reactive astrogliosis, neurological disorders, astrocyte dysfunction
- MeSH terms
- Animals, Astrocytes, Brain, Humans, Neuronal Plasticity, Neurodegenerative Diseases
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