Evidence map›Paper›PMID 29227284›Full record

ArticleThe Journal of clinical investigation2018

Cografting astrocytes improves cell therapeutic outcomes in a Parkinson's disease model.

Jae-Jin Song, Sang-Min Oh, Oh-Chan Kwon, Noviana Wulansari, Hyun-Seob Lee, Mi-Yoon Chang, Eunsoo Lee, Woong Sun, Sang-Eun Lee, Sunghoe Chang and 3 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

57 citing papers in PubMed, 76 citations in OpenAlex.

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  12. Characterization of Isolated Human Astrocytes from Aging Brain.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 4 countries.

Jae-Jin SongDepartment of Biochemistry and Molecular Biology, College of Medicine.
Sang-Min OhDepartment of Biochemistry and Molecular Biology, College of Medicine.
Oh-Chan KwonDepartment of Biochemistry and Molecular Biology, College of Medicine.
Noviana WulansariDepartment of Biochemistry and Molecular Biology, College of Medicine.
Hyun-Seob LeeGenomic Core Facility, Transdisciplinary Research and Collaboration Division, Translational Research Institute, and.
Mi-Yoon ChangDepartment of Biochemistry and Molecular Biology, College of Medicine.
Eunsoo LeeDepartment of Anatomy and Division of Brain Korea 21 PLUS Program for Biomedical Science, Korea University College of Medicine, Seoul, South Korea.
Woong SunDepartment of Anatomy and Division of Brain Korea 21 PLUS Program for Biomedical Science, Korea University College of Medicine, Seoul, South Korea.
Sang-Eun LeeDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Sunghoe ChangDepartment of Physiology and Biomedical Sciences, Seoul National University College of Medicine, Seoul, South Korea.
Heeyoung AnCenter for Neuroscience and.
C Justin LeeCenter for Neuroscience and.
Sang-Hun LeeDepartment of Biochemistry and Molecular Biology, College of Medicine.
Biomedical Research Institute · USSeoul National University · KRKorea University · JPKorea University · KRTranslational Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transplantation of neural progenitor cells (NPCs) is a potential therapy for treating neurodegenerative disorders, but this approach has faced many challenges and limited success, primarily because of inhospitable host brain environments that interfere with enriched neuron engraftment and function. Astrocytes play neurotrophic roles in the developing and adult brain, making them potential candidates for helping with modification of hostile brain environments. In this study, we examined whether astrocytic function could be utilized to overcome the current limitations of cell-based therapies in a murine model of Parkinson's disease (PD) that is characterized by dopamine (DA) neuron degeneration in the midbrain. We show here that cografting astrocytes, especially those derived from the midbrain, remarkably enhanced NPC-based cell therapeutic outcomes along with robust DA neuron engraftment in PD rats for at least 6 months after transplantation. We further show that engineering of donor astrocytes with Nurr1 and Foxa2, transcription factors that were recently reported to polarize harmful immunogenic glia into the neuroprotective form, further promoted the neurotrophic actions of grafted astrocytes in the cell therapeutic approach. Collectively, these findings suggest that cografting astrocytes could be a potential strategy for successful cell therapeutic outcomes in neurodegenerative disorders.

Indexed as

AnimalsAstrocytesDisease Models, AnimalHepatocyte Nuclear Factor 3-betaMesencephalonMiceNeural Stem CellsNuclear Receptor Subfamily 4, Group A, Member 2Parkinson Disease, SecondaryRatsRats, Sprague-DawleyFoxa2 protein, mouseFoxa2 protein, ratHepatocyte Nuclear Factor 3-betaNr4a2 protein, mouseNr4a2 protein, ratNuclear Receptor Subfamily 4, Group A, Member 2Neuronal stem cellsNeuroscienceParkinson’s diseaseTransplantation

Identifiers

PMID29227284
PMCPMC5749514
OpenAlexW2774430083

What OpenQuestion holds

Textmetadata
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.