Evidence map›Paper›PMID 41639424›Full record

ReviewExperimental & molecular medicine2026

The rise of astrocytes: are they guardians or troublemakers of the brain disorder?

Hee Yeon Kim, Seungchan Kim, Asli Nur Akaydin, Suhyun Kim, Seung Jae Hyeon, Junghee Lee, Hoon Ryu

Abstract 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. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hee Yeon Kim *Brain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Seungchan Kim *Brain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0000-1645-6422
Asli Nur Akaydin *Brain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0009-7888-6992
Suhyun KimBrain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Seung Jae HyeonBrain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Junghee LeeBoston University Alzheimer's Disease Research Center and Department of Neurology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA. junghee@bu.edu.ORCID http://orcid.org/0000-0002-9530-9806
Hoon RyuBrain Gene Regulation and Epigenetics Laboratory, Center for Brain Disorders, Brain Science Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea. hoonryu@kist.re.kr.ORCID http://orcid.org/0000-0001-6544-3732

Funding

Modulation of neuronal atrophy in Huntington's diseaseR01NS109537 · NINDS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LEE, JUNGHEE · 2018 to 2022
$1.4M
Korea Institute of Science and Technology (KIST) 2E33411Korea Institute of Science and Technology (KIST) 2E33701National Research Foundation of Korea (NRF) NRF-2020M3E5D9079742National Research Foundation of Korea (NRF) NRF2021R1C1C2095827National Research Foundation of Korea (NRF) NRF-2022R1A2C3013138National Research Foundation of Korea (NRF) NRF-2022R1A6A3A01086375National Research Foundation of Korea (NRF) RS-2024-00461291NINDS NIH HHS R01 NS109537U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01NS109537
6 · The paper itself

Abstract

The brain is a highly complex, multicellular organ composed of diverse neuronal and nonneuronal cell types that function in concert to maintain central nervous system homeostasis. Among the glial populations, astrocytes are critical regulators of neuronal function. Under physiological conditions, astrocytes provide essential metabolic support, modulate neurotransmitter release and maintain neuronal health. Traditionally viewed as passive and supporting cells, astrocytes are now recognized as dynamic and responsive elements within the central nervous system. In response to pathological insults, astrocytes undergo significant changes in function, morphology and gene expression-a process known as reactive astrogliosis. Reactive astrocytes acquire heterogeneous characteristics that can contribute to brain disorders via the non-cell-autonomous mechanisms. However, the drivers of this transformation-and their shift from neuronal guardians to potential contributors to pathology-remain incompletely understood. Here we explore the complex, multidimensional roles of astrocytes and how reactive states alter their primary functions. We focus on the dual protective and pathological roles of astrocytes, particularly the transition from healthy to heterogeneous reactive forms, with the aim of understanding their overall impact on the progression of neurodegenerative diseases.

Indexed as

AstrocytesBrain DiseasesAnimalsBrainHumansNeurodegenerative Diseases

Identifiers

PMID41639424
PMCPMC12992555

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.