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


Journal

Molecular brain
ISSN: 1756-6606
Titre abrégé: Mol Brain
Pays: England
ID NLM: 101468876

Informations de publication

Date de publication:
08 11 2021
Historique:
received: 14 09 2021
accepted: 28 10 2021
entrez: 9 11 2021
pubmed: 10 11 2021
medline: 5 4 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34749773
doi: 10.1186/s13041-021-00874-8
pii: 10.1186/s13041-021-00874-8
pmc: PMC8573876
doi:

Substances chimiques

Amino Acid Transport System y+ 0
Amino Acid Transport Systems, Neutral 0
Glial Fibrillary Acidic Protein 0
Olig2 protein, mouse 0
Oligodendrocyte Transcription Factor 2 0
Slc7a10 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

163

Informations de copyright

© 2021. The Author(s).

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Auteurs

Kouko Tatsumi (K)

Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan. radha815@naramed-u.ac.jp.

Kaoru Kinugawa (K)

Department of Neurology, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Ayami Isonishi (A)

Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Masahiro Kitabatake (M)

Department of Immunology, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Hiroaki Okuda (H)

Department of Anatomy, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa, 920-1192, Japan.

Shoko Takemura (S)

Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Tatsuhide Tanaka (T)

Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Eiichiro Mori (E)

Department of Future Basic Medicine, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

Akio Wanaka (A)

Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University, Kashihara, Nara, 634-8521, Japan.

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