Glucose transporter expression in brain. cDNA sequence of mouse GLUT3, the brain facilitative glucose transporter isoform, and identification of sites of expression by in situ hybridization.
Open accessAbstract
Complementary DNAs encoding the mouse GLUT3/brain facilitative glucose transporter have been isolated and sequenced. The predicted amino acid sequence indicates that mouse GLUT3 is composed of 493 amino acids and has 83 and 89% identity and similarity, respectively, to the sequence of human GLUT3. In contrast to human GLUT3 mRNA, which can be readily detected by RNA blotting in all human tissues that have been examined, mouse GLUT3 mRNA was only present at significant levels in brain. In situ hybridization showed differential expression of GLUT3 mRNA in several regions of adult mouse brain. Specific expression was observed in the hippocampus, with GLUT3 mRNA levels being higher in areas CA1 to CA3 than in the dentate gyrus. It was also detected in the Purkinje cell layer of the cerebellum and in the cerebral cortex, with higher expression in the piriform cortex than in other regions of the cortex. Antisera to mouse GLUT3 immunoblotted a series of proteins of 45-50 kDa in mouse brain plasma membranes. These results are consistent with GLUT3 being a neuronal glucose transporter.
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GLUT3 is the predominant isoform in neuron populations.
“GLUT3 is the predominant isoform in the neuron populations (Nagamatsu et al., 1992)”
From Human ApoE Isoforms Differentially Modulate Brain Glucose and Ketone Body Metabolism: Implications for Alzheimer's Disease Risk Reduction and Early Intervention (2018) · cites this paper as Nagamatsu et al., 1992
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- Authors
- Nagamatsu, S., Kornhauser, J. M., Burant, C. F., Seino, S., Mayo, K. E., & Bell, G. I.
- Affiliations
- Northwestern University (US)
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1992-01
- Volume
- 267
- Issue
- 1
- Pages
- 467-472
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1543414021
- Cited by
- 262
- References
- 1
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 5 · 2023: 3 · 2022: 5 · 2021: 1 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 4 · 2016: 2 · 2015: 5 · 2014: 4 · 2013: 3 · 2012: 2
- FWCI
- 9.27
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 20595, DK42086, P30DK042086)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (P01HD021921, HD 21921)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- GLUT3, glucose transporters, brain glucose transport, cDNA sequence, hippocampus, cerebellum, cerebral cortex, piriform cortex, plasma membrane
- MeSH terms
- Amino Acid Sequence, Animals, Base Sequence, Brain, Cell Membrane, DNA, Glucose, Humans, Molecular Sequence Data, Monosaccharide Transport Proteins, Nerve Tissue Proteins, Nucleic Acid Hybridization, RNA, Messenger, Sequence Homology, Nucleic Acid, Blotting, Western, Gene Expression, Glucose Transporter Type 3, Mice
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