New Insights into Astrocytes in Health and Disease

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Neuroscience".

Deadline for manuscript submissions: closed (20 June 2026) | Viewed by 2230

Editor

Salk Institute for Biological Studies, 10010 N Torrey Pine Rd, La Jolla, CA 92037, USA
Interests: astrocyte; neuronal development; AAV; crispr; Alzheimer's disease; neurodegeneration; rho GTPase

Special Issue Information

Dear Colleagues,

Astrocytes are a type of glial cell in the nervous system that perform a wide range of functions in both health and disease. Recent advances in astrocyte research have highlighted their critical roles in synaptic modulation and interactions with other cell types, including microglia and oligodendrocytes. Astrocytes are also essential for maintaining the blood–brain barrier (BBB) and controlling the exchange of ions and molecules between the bloodstream and the brain parenchyma. Furthermore, astrocytes play a central role in brain metabolism and neuroinflammation. Bulk and single-cell transcriptomic analyses from both human and mouse brains have identified novel astrocyte subtypes in health and disease, as well as common transcriptomic changes across diseases and disease-specific alterations, further highlighting their diverse and dynamic functions in the central nervous system. The objective of this Special Issue is to provide new insights into astrocyte function in health and diseases, with topics including, but not limited to, the following:

  • Astrocyte heterogeneity;
  • Blood–brain barrier (BBB);
  • Synaptic modulation;
  • Metabolic support;
  • Neuroinflammation;
  • Ageing;
  • Neurodegenerative disorders;
  • Neurodevelopmental disorders;
  • Stress response.

Dr. Tao Tao
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as communications are invited. For planned papers, a title and short abstract (about 250 words) can be sent to the Editorial Office for assessment.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-anonymized peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cells is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • astrocytes heterogeneity
  • blood-brain barrier (BBB)
  • synaptic modulation
  • metabolic support
  • neuroinflammation
  • ageing
  • neurodegenerative disorders
  • neurodevelopmental disorders
  • stress response

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

27 pages, 18962 KB  
Article
Astrocyte Diversity and Alcohol-Related Gliovascular Alterations in the Human Dorsal Striatum Revealed by Combined Morphometric and Ultrastructural Analyses
by Evalds Viguls, Anita Ilze Gulbe, Simons Svirskis, Valerija Groma and Sandra Skuja
Cells 2026, 15(10), 892; https://doi.org/10.3390/cells15100892 - 14 May 2026
Viewed by 1072
Abstract
Astrocytes are key regulators of neuronal, metabolic, and vascular homeostasis, yet their morphological diversity and involvement in alcohol-related brain pathology remain incompletely characterized. In this study, we investigated astrocytic morphology in the human striatum of control individuals and subjects with short- and long-term [...] Read more.
Astrocytes are key regulators of neuronal, metabolic, and vascular homeostasis, yet their morphological diversity and involvement in alcohol-related brain pathology remain incompletely characterized. In this study, we investigated astrocytic morphology in the human striatum of control individuals and subjects with short- and long-term alcohol exposure using immunohistochemistry combined with Sholl-based morphometric analysis, and ultrastructural assessment. GFAP immunohistochemistry was used to identify astrocytes, assess their morphology, and manually quantify GFAP+ cells in gray and white matter, followed by Sholl-based morphometric analysis to characterize astrocytic branching architecture and spatial organization. The number of GFAP+ astrocytes differed between tissue compartments, with a significant increase in white matter in alcohol-exposed individuals and no detectable change in gray matter. Morphometric analysis revealed pronounced astrocytic heterogeneity across all study groups. Sholl-derived metrics supported the distinction of six recurrent astrocytic morphometric profiles in the human striatum, distinguished by soma size, branching complexity, process length, and cell territory size. These profiles were present across gray and white matter, indicating intrinsic astrocytic structural diversity. Ultrastructural analysis further revealed alcohol-associated alterations at the astrocyte–vascular interface, including swelling of perivascular astrocytic endfeet, accumulation of intermediate filaments, and focal reductions in vascular wall coverage. Together, these findings demonstrate substantial astrocytic structural diversity in the human striatum accompanied by alcohol-related gliovascular remodeling. Full article
(This article belongs to the Special Issue New Insights into Astrocytes in Health and Disease)
Show Figures

Graphical abstract

27 pages, 17496 KB  
Article
Running Exercise Promotes Astrocyte-Mediated Structural Plasticity in the Amygdalar BLA and CeA to Alleviate Anhedonia-like Behavior Alterations
by Xinyan Ren, Yanmin Luo, Qian Xiao, Jing Li, Yuning Zhou, Yuhui Deng, Xingyu Wu, Huifang Luo, Yue Li, Lin Jiang, Chunni Zhou, Dujuan Huang, Xiaoyun Dou, Fenglei Chao, Lei Zhang, Xin Liang, Yong Tang and Jing Tang
Cells 2026, 15(8), 693; https://doi.org/10.3390/cells15080693 - 14 Apr 2026
Viewed by 597
Abstract
Amygdala dysfunction is implicated in stress-related affective disorders, and astrocytes are key regulators of amygdalar neuroplasticity. Here, we examined whether running exercise modulates astrocyte number, morphology, proliferation, and excitatory synaptic contacts in the basolateral amygdala (BLA) and central amygdala (CeA) in rats exposed [...] Read more.
Amygdala dysfunction is implicated in stress-related affective disorders, and astrocytes are key regulators of amygdalar neuroplasticity. Here, we examined whether running exercise modulates astrocyte number, morphology, proliferation, and excitatory synaptic contacts in the basolateral amygdala (BLA) and central amygdala (CeA) in rats exposed to chronic unpredictable stress (CUS). Anhedonia-like behaviors were evaluated using the sucrose preference test, while anxiety-related behaviors were assessed using the elevated plus maze and open field tests. Unbiased stereological three-dimensional quantification was used to assess amygdalar volume and estimate astrocyte numbers in BLA and CeA, and immunofluorescence with morphological reconstruction was performed to quantify astrocytic complexity, proliferation, and astrocyte-associated PSD95+ puncta. Running exercise significantly increased sucrose preference in CUS rats, whereas elevated plus maze and open field measures were not significantly changed. CUS reduced astrocyte number and proliferation, and induced astrocytic morphological atrophy in both subregions. These alterations were reversed by running. Moreover, running increased the number of excitatory synapses contacted by astrocytes in the BLA and CeA of CUS rats. These findings suggest that running promotes astrocyte-mediated structural remodeling in amygdalar subregions, which may contribute to the regulation of anhedonia-like behavioral alterations associated with chronic stress. Full article
(This article belongs to the Special Issue New Insights into Astrocytes in Health and Disease)
Show Figures

Figure 1

Back to TopTop