Evidence map›Paper›PMID 34749773›Full record

ArticleMolecular brain2021

Olig2-astrocytes express neutral amino acid transporter SLC7A10 (Asc-1) in the adult brain.

Kouko Tatsumi, Kaoru Kinugawa, Ayami Isonishi, Masahiro Kitabatake, Hiroaki Okuda, Shoko Takemura, Tatsuhide Tanaka, Eiichiro Mori, Akio Wanaka

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Genes · 2025
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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

9 authors at 2 institutions in 1 country.

Kouko Tatsumi *Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan. radha815@naramed-u.ac.jp.ORCID 0000-0001-6230-2803
Kaoru Kinugawa *Department of Neurology, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Ayami IsonishiDepartment of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Masahiro KitabatakeDepartment of Immunology, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Hiroaki OkudaDepartment of Anatomy, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa, 920-1192, Japan.
Shoko TakemuraDepartment of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Tatsuhide TanakaDepartment of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Eiichiro MoriDepartment of Future Basic Medicine, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Akio WanakaDepartment of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.
Nara Medical University · JPKanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have reported that the transcription factor Olig2 labels a subpopulation of astrocytes (Olig2-astrocytes), which show distribution patterns different from those of GFAP-expressing astrocytes (GFAP-astrocytes) in the adult brain. Here, to uncover the specific functions of Olig2-astrocytes, we first analyzed public single-cell RNA-seq databases of adult mouse brains. Unbiased classification of gene expression profiles and subsequent gene ontology analyses revealed that the majority of Olig2-astrocytes belonged to an astrocytic cluster that is enriched for transporter-related genes. SLC7A10 (also known as ASC-1) was one of the representative neutral amino acid transporter genes in the cluster. To complement the in silico data analyses, we differentially isolated Olig2- and GFAP-astrocytes from the same frozen section of the lateral globus pallidus using laser microdissection and compared their gene expression by quantitative reverse transcription PCR. We confirmed that Olig2 and GFAP mRNAs were preferentially expressed in the Olig2- and GFAP-astrocytes, respectively, indicating that the laser microdissection method yielded minimal cross-contamination between two types of cells. The Olig2-astrocytes expressed significantly higher levels of SLC7A10 mRNA than the GFAP-astrocytes, corroborating the in silico data. We next localized SLC7A10 protein by immunohistochemistry in the lateral globus pallidus, which was also genetically labeled for Olig2. SLC7A10 co-localized with Olig2-genetic labeling, especially on the fine processes of Olig2-astrocytes. These results are consistent with the recent discovery that SLC7A10 is expressed not only in neurons but also in a subset of astrocytes. Taken together, our findings suggest that SLC7A10 exerts specific functions in Olig2-astrocytes of the adult brain.

Indexed as

Amino Acid Transport Systems, NeutralBrain InjuriesAmino Acid Transport System y+AnimalsAstrocytesBrainGlial Fibrillary Acidic ProteinMiceNeuronsOligodendrocyte Transcription Factor 2Amino Acid Transport Systems, NeutralAmino Acid Transport System y+Glial Fibrillary Acidic ProteinOlig2 protein, mouseOligodendrocyte Transcription Factor 2Slc7a10 protein, mouse

Identifiers

PMID34749773
PMCPMC8573876
OpenAlexW3213855297

What OpenQuestion holds

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Registered trials

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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.