The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Vesicular Neurotransmitter Transporter Expression in Developing Postnatal Rodent Retina: GABA and Glycine Precede Glutamate
Open accessAbstract
Vesicular transporters regulate the amount and type of neurotransmitter sequestered into synaptic vesicles and, hence, the kind of signal transmitted to postsynaptic neurons. Glutamate is the prominent excitatory neurotransmitter in retina; GABA and glycine are the main inhibitory neurotransmitters. Little is known about the ontogeny of vesicular neurotransmission in retina. We investigated expression of glutamatergic [vesicular glutamate transporter 1 (VGLUT1)] and GABA/glycinergic [vesicular GABA/glycine transporter (VGAT)] vesicular transporters in postnatal retina. VGLUT1 labels glutamatergic synapses. VGLUT1 and synaptic vesicle 2 colocalized to photoreceptor terminals. VGLUT1 colocalized with PKC to rod bipolar terminals and to ON bipolar terminals in metabotropic glutamate receptor 6+/- mice. Developmentally, VGAT expression precedes VGLUT1. In rat and mouse retina, VGAT occurred in the inner retina by postnatal day 1 (P1). In rat retina, VGLUT1 was in the outer retina by P5-P7 and the inner retina by P7. In the mouse retina, VGLUT1 expression was in the outer retina by P3 and the inner retina by P5. Both rat and mouse retina had an adult pattern of VGLUT1 expression by P14. VGLUT1 expression precedes ribbon synapses, which are first observed in the inner retina at P11 (Fisher, 1979) in mouse and P13 (Horsburgh and Sefton, 1987) in rat. The ribbon synapse marker RIBEYE was not detected in inner retina of P5 or P7 rat. Spontaneous EPSCs in mouse ganglion cells were recorded as early as P7. Together, these findings indicate that vesicular GABA and glycine transmission precedes vesicular glutamate transmission in developing rodent retina. Furthermore, vesicular glutamate transmission likely occurs before ribbon synapse formation in the inner retina.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“We examined changes in endogenous vesicular glutamate transporter 1 (VGLUT-1), a presynaptic protein expressed at bipolar ribbon synapses [37], and postsynaptic density protein 95 (PSD95) in the inner plexiform layer, where RGC dendrites are located.”
From AMPK hyperactivation promotes dendrite retraction, synaptic loss, and neuronal dysfunction in glaucoma (2021) · cites this paper as [37]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The Expression of Vesicular Glutamate Transporters Defines Two Classes of Excitatory Synapse
Fremeau, R. T., Troyer, M. D., Pahner, I., Nygaard, G. O., Tran, C. H., Reimer, R. J., Bellocchio, E. E., Fortin, D. L., Storm‐Mathisen, J., & Edwards, R. H. (2001) · Neuron · doi:10.1016/s0896-6273(01)00344-0 · Cited by 1,266
Self-citationIdentification and characterization of the vesicular GABA transporter
McIntire, S. L., Reimer, R. J., Schuske, K., Edwards, R. H., & Jørgensen, E. M. (1997) · Nature · doi:10.1038/39908 · Cited by 886
Self-citationTakamori, S., Rhee, J. S., Rosenmund, C., & Jahn, R. (2000) · Nature · doi:10.1038/35025070 · Cited by 862
Uptake of Glutamate into Synaptic Vesicles by an Inorganic Phosphate Transporter
Bellocchio, E. E., Reimer, R. J., Fremeau, R. T., & Edwards, R. H. (2000) · Science · doi:10.1126/science.289.5481.957 · Cited by 795
Self-citationBuckley, K. M., & Kelly, R. B. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.4.1284 · Cited by 713
Chaudhry, F. A., Reimer, R. J., Bellocchio, E. E., Danbolt, N. C., Osen, K. K., Edwards, R. H., & Storm‐Mathisen, J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-23-09733.1998 · Cited by 640
Self-citationRIBEYE, a Component of Synaptic Ribbons
Schmitz, F., Königstorfer, A., & Südhof, T. C. (2000) · Neuron · doi:10.1016/s0896-6273(00)00159-8 · Cited by 581
Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals
von Gersdorff, H., & Mathews, G. (1994) · Nature · doi:10.1038/367735a0 · Cited by 457
Rod bipolar cells in the mammalian retina show protein kinase C‐like immunoreactivity
Greferath, U., Grünert, U., & Wässle, H. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010308 · Cited by 420
Lee, R., Sawin, E. R., Chalfie, M., Horvitz, H. R., & Avery, L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00159.1999 · Cited by 351
Immunocytochemical identification of cone bipolar cells in the rat retina
Euler, T., & Wässle, H. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903610310 · Cited by 347
Bellocchio, E. E., Hu, H., Pohorille, A., Chan, J., Pickel, V. M., & Edwards, R. H. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08648.1998 · Cited by 337
Self-citationNi, B., Rosteck, P. R., Nadi, N. S., & Paul, S. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.12.5607 · Cited by 316
Evidence That Vesicles on the Synaptic Ribbon of Retinal Bipolar Neurons Can Be Rapidly Released
von Gersdorff, H., Vardi, E., Matthews, G., & Sterling, P. (1996) · Neuron · doi:10.1016/s0896-6273(00)80148-8 · Cited by 300
The Cone Pedicle, a Complex Synapse in the Retina
Haverkamp, S., Grünert, U., & Wässle, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00011-8 · Cited by 262
Release of endogenous excitatory amino acids from turtle photoreceptors
Copenhagen, D. R., & Jahr, C. E. (1989) · Nature · doi:10.1038/341536a0 · Cited by 252
Self-citationImmunocytochemical Localization of the Postsynaptic Density Protein PSD-95 in the Mammalian Retina
Koulen, P., Fletcher, E. L., Craven, S. E., Bredt, D. S., & Wässle, H. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-23-10136.1998 · Cited by 230
Synaptic Vesicle Transporter Expression Regulates Vesicle Phenotype and Quantal Size
Pothos, E. N., Larsen, K. E., Krantz, D. E., Liu, Y., Haycock, J. W., Setlik, W., Gershon, M. D., Edwards, R. H., & Sulzer, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07297.2000 · Cited by 211
Self-citationDevelopmentally Regulated Spontaneous Activity in the Embryonic Chick Retina
Wong, W. T., Sanes, J. R., & Wong, R. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08839.1998 · Cited by 189
Cellular degeneration and synaptogenesis in the developing retina of the rat
Horsburgh, G. M., & Sefton, A. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902630407 · Cited by 179
Takamori, S., Riedel, D., & Jahn, R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-13-04904.2000 · Cited by 177
The rod bipolar cell of the mammalian retina
Wässle, H., Yamashita, M., Greferath, U., Grünert, U., & Müller, F. U. (1991) · Visual Neuroscience · doi:10.1017/s095252380001097x · Cited by 170
Rieke, F., & Schwartz, E. A. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021360 · Cited by 161
Development of synaptic arrays in the inner plexiform layer of neonatal mouse retina
Fisher, L. J. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870207 · Cited by 158
Visual Deprivation Alters Development of Synaptic Function in Inner Retina after Eye Opening
Tian, N., & Copenhagen, D. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00470-6 · Cited by 156
Self-citationVu, T. Q., Payne, J. A., & Copenhagen, D. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-04-01414.2000 · Cited by 142
Self-citationZhou, Z., & Zhao, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06570.2000 · Cited by 113
von Kriegstein, K., Schmitz, F., Link, E., & Südhof, T. C. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00542.x · Cited by 113
Tachibana, M., & Okada, T. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-07-02199.1991 · Cited by 113
Exaggerated astrocyte reactivity after nigrostriatal deafferentation in the aged rat
Gordon, M. N., Schreier, W. A., Ou, X., Holcomb, L. A., & Morgan, D. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971110)388:1 · Cited by 111
Tagawa, Y., Sawai, H., Ueda, Y., Tauchi, M., & Nakanishi, S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-07-02568.1999 · Cited by 95
Vesicular γ‐aminobutyric acid transporter expression in amacrine and horizontal cells
Cueva, J. G., Haverkamp, S., Reimer, R. J., Edwards, R. H., Wässle, H., & Brecha, N. C. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10166 · Cited by 84
Self-citationAnalysis of excitatory and inhibitory spontaneous synaptic activity in mouse retinal ganglion cells.
Tian, N., Hwang, T. N., & Copenhagen, D. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1327 · Cited by 81
Self-citationNeurotransmitter release at ribbon synapses in the retina
Morgans, C. W. (2000) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2000.00923.x · Cited by 66
Presynaptic proteins of ribbon synapses in the retina
Morgans, C. W. (2000) · Microscopy Research and Technique · doi:10.1002/1097-0029(20000715)50:2 · Cited by 54
Rörig, B., & Grantyn, R. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90088-r · Cited by 52
GABA-induced increases in [Ca2+]i in retinal neurons of postnatal rabbits
Huang, B., & Redburn, D. A. (1996) · Visual Neuroscience · doi:10.1017/s0952523800008117 · Cited by 46
Zhou, Z. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05158.2001 · Cited by 41
Regulation of transmitter release from retinal bipolar cells
Tachibana, M. (1999) · Progress in Biophysics and Molecular Biology · doi:10.1016/s0079-6107(99)00003-6 · Cited by 39
Bähring, R., Standhardt, H., Martelli, E. A., & Grantyn, R. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00606.x · Cited by 26
Developmental expression of a synaptic ribbon antigen (B16) in mouse retina
Bachman, K. M., & Balkema, G. W. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903330109 · Cited by 18
Huang, B., Mitchell, C. K., & REDBURN-JOHNSON, D. A. (2000) · Visual Neuroscience · doi:10.1017/s0952523800176126 · Cited by 16
Cited by
Sorted by citations
Functional architecture of the retina: Development and disease
Hoon, M., Okawa, H., Santina, L. D., & Wong, R. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2014.06.003 · Cited by 628
Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3
Seal, R. P., Akil, O., Yi, E., Weber, C. M., Grant, L. M., Yoo, J. W., Clause, A. R., Kandler, K., Noebels, J. L., Glowatzki, E., et al. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.032 · Cited by 414
Self-citationTypes of bipolar cells in the mouse retina
Ghosh, K. K., Bujan, S., Haverkamp, S., Feigenspan, A., & Wässle, H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10985 · Cited by 378
Visual Stimulation Is Required for Refinement of ON and OFF Pathways in Postnatal Retina
Tian, N., & Copenhagen, D. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00389-1 · Cited by 304
Self-citationLateral interactions in the outer retina
Thoreson, W. B., & Mangel, S. C. (2012) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2012.04.003 · Cited by 253
Metadata
- Authors
- Johnson, J., Tian, N., Caywood, M. S., Reimer, R. J., Edwards, R. H., & Copenhagen, D. R.
- Affiliations
- Yale University (US)
- Stanford Medicine (US)
- University of California, San Francisco (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2003-01-15
- Volume
- 23
- Issue
- 2
- Pages
- 518-529
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6741860
- OpenAlex
- W1545065700
- Cited by
- 197
- References
- 42
- Citations by year
- 2025: 4 · 2024: 5 · 2023: 8 · 2022: 9 · 2021: 11 · 2020: 5 · 2019: 3 · 2018: 7 · 2017: 6 · 2016: 8 · 2015: 5 · 2014: 7 · 2013: 17 · 2012: 13
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Research to Prevent Blindness
- That Man May See
- National Institutes of Health
- National Eye Institute (R01EY001869)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- VGLUT1, vesicular GABA transporter, glutamatergic synapses, GABAergic synapses, photoreceptor terminals, rod bipolar cells, ON bipolar cells, mGluR6, protein kinase C, ribeye, spontaneous EPSCs, retinal ganglion cells
- MeSH terms
- Age Factors, Animals, Carrier Proteins, gamma-Aminobutyric Acid, Glycine, Heterozygote, Membrane Glycoproteins, Membrane Proteins, Mice, Inbred C57BL, Mice, Mutant Strains, Nerve Tissue Proteins, Neurons, Retina, Retinal Ganglion Cells, Presynaptic Terminals, Patch-Clamp Techniques, Glutamic Acid, Excitatory Postsynaptic Potentials, Rats, Long-Evans, Photoreceptor Cells, Vertebrate, Membrane Transport Proteins, Organic Anion Transporters, Vesicular Transport Proteins, GABA Plasma Membrane Transport Proteins, Vesicular Glutamate Transport Protein 1, Mice, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review