Evidence map›Paper›PMID 42032208›Full record

ReviewExperimental & molecular medicine2026

Curing the brain: in search for new astrocyte-specific therapies.

Alexei Verkhratsky, C Justin Lee, Heejung Chun, Christian Göritz, Tibor Harkany, Jae-Hun Lee, Sangkyu Lee, Maria Lindskog, Wuhyun Koh, Jan Mulder and 16 more

Erratum issuedAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors.

Alexei VerkhratskyFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK. Alexej.Verkhratsky@manchester.ac.uk.
C Justin LeeCenter for Memory and Glioscience, Institute for Basic Science, Daejeon, Republic of Korea. cjl@ibs.re.kr.ORCID http://orcid.org/0000-0002-3555-0980
Heejung ChunCollage of Pharmacy, Yonsei-SL Institute, Yonsei University, Incheon, Republic of Korea.ORCID http://orcid.org/0000-0002-6451-1542
Christian GöritzDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0799-766X
Tibor HarkanyDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Jae-Hun LeeCenter for Memory and Glioscience, Institute for Basic Science, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0003-2317-9958
Sangkyu LeeCenter for Memory and Glioscience, Institute for Basic Science, Daejeon, Republic of Korea.
Maria LindskogDepartment of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Wuhyun KohCenter for Memory and Glioscience, Institute for Basic Science, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-4398-1094
Jan MulderDepartment of Neuroscience, Karolinska Institutet, Solna, Sweden.
Min-Ho NamCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-6191-1268
Ole Petter OttersenInstitute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Marcela PeknaDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Milos PeknyDepartment of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Aleksandra PękowskaDioscuri Centre for Chromatin Biology and Epigenomics, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Hoon RyuCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Chang Ho SohnGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
Evgenii O TretiakovDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Verena UntietDivision of Astrocyte Driven Ionostasis, Center for Translational Neuromedicine, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-1888-6378
Tim J VineyDepartment of Pharmacology, University of Oxford, Oxford, UK.
Wongu YounCenter for Memory and Glioscience, Institute for Basic Science, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0001-6807-141X
Chenju YiDepartment of Geriatrics, Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.
Robert ZorecCelica, BIOMEDICAL, Ljubljana, Slovenia.
Mijin YunDepartment of Nuclear Medicine, Yonsei Univserity College of Medicine, Seoul, Republic of Korea.
Eunji CheongDepartment of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea. eunjicheong@yonsei.ac.kr.
Agneta NordbergDepartment of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Karolinska institutet, Stockholm, Sweden. agneta.k.nordberg@ki.se.

Funding

Alzheimerfonden AF-994908Forskningsrådet om Hälsa, Arbetsliv och Välfärd (Swedish Research Council for Health, Working Life and Welfare) VR-2023-02656Institute for Basic Science (IBS) IBS-R001-Y4National Research Foundation of Korea (NRF) 2021R1A2C3007164 and 2022M3E5E8016325National Research Foundation of Korea (NRF) RS-2021-NR061245National Research Foundation of Korea (NRF) RS-2024-00397737
6 · The paper itself

Abstract

Astroglia, an extended class of homeostatic and defensive cells of the central nervous system (CNS), contribute to the pathogenesis of all known neurological and neuropsychiatric disorders. The pathophysiology of astrocytes is complex, mutable, disease and disease-stage specific. In neuroinflammatory lesions and in various chronic conditions, astrocytes undergo an evolutionary conserved defensive remodeling known as reactive astrogliosis, which produces highly heterogeneous reactive astrocytic phenotypes. Broadly, reactive astrogliosis can be classified into proliferative anysomorphic barrier-forming astrogliosis characteristic of traumatic CNS lesions and nonproliferative isomorphic gliosis widely manifested in chronic neuropathologies. In addition, in many pathologies, astrocytes undergo atrophy and asthenia with resulting loss of homeostatic support and neuroprotection precipitating neuronal damage. Reactive and atrophic astrocytes may coexist or emerge in sequence in a disease-stage-dependent manner. Several classes of astrocyte-specific molecules and processes implicated in various diseases of the CNS represent therapeutic targets. Astrocyte-specific therapeutic strategies may improve both disease-preventing and disease-modifying therapeutic outcomes.

Indexed as

AstrocytesBrainAnimalsGliosisHumans

Identifiers

PMID42032208
PMCPMC13144692

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.