The neuronal form of adaptor protein-3 is required for synaptic vesicle formation from endosomes
Open accessAbstract
Heterotetrameric adaptor complexes vesiculate donor membranes. One of the adaptor protein complexes, AP-3, is present in two forms; one form is expressed in all tissues of the body, whereas the other is restricted to brain. Mice lacking both the ubiquitous and neuronal forms of AP-3 exhibit neurological disorders that are not observed in mice that are mutant only in the ubiquitous form. To begin to understand the role of neuronal AP-3 in neurological disease, we investigated its function in in vitro assays as well as its localization in neural tissue. In the presence of GTPgammaS both ubiquitous and neuronal forms of AP-3 can bind to purified synaptic vesicles. However, only the neuronal form of AP-3 can produce synaptic vesicles from endosomes in vitro. We also identified that the expression of neuronal AP-3 is limited to varicosities of neuronal-like processes and is expressed in most axons of the brain. Although the AP-2/clathrin pathway is the major route of vesicle production and the relatively minor neuronal AP-3 pathway is not necessary for viability, the absence of the latter could lead to the neurological abnormalities seen in mice lacking the expression of AP-3 in brain. In this study we have identified the first brain-specific function for a neuronal adaptor complex.
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
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?
Ap3b2 is a neuron-specific gene involved in synaptic vesicle formation, transfer of membrane proteins to lysosomes, and endocytosis.
“Interestingly, the most significantly down-regulated gene, Ap3b2, is a neuron-specific gene and is involved in the formation of synaptic vesicles, transfer of membrane proteins to lysosomes, and endocytosis (42, 43).”
From The effect of Abi3 locus deletion on the progression of Alzheimer’s disease-related pathologies (2023) · cites this paper as [42]
The Localization of β3B section (page not provided) describes β3B-containing AP-3 as neuronal-specific, and the Discussion (Fig. 8; page not provided) supports its role in forming synaptic vesicles from endosomes. The Discussion does not establish that neuronal AP-3 transfers membrane proteins to lysosomes; it instead proposes that AP-3 may rescue some proteins from lysosomal degradation. It assigns endocytosis from the plasma membrane primarily to the separate AP-2/clathrin pathway. (LLM, conf=0.87)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Kirchhausen, T. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.699 · Cited by 560 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
v-SNARE composition distinguishes synaptic vesicle pools
Hua, Z., Leal-Ortiz, S., Foss, S. M., Waites, C. L., Garner, C. C., Voglmaier, S. M., & Edwards, R. H. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.010 · Cited by 168 · see citing works
The effect of Abi3 locus deletion on the progression of Alzheimer’s disease-related pathologies
Karahan, H., Smith, D. C., Kim, B., McCord, B., Mantor, J., John, S. K., Al-Amin, M. M., Dabin, L. C., & Kim, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1102530 · Cited by 20 · see citing works
“Interestingly, the most significantly down-regulated gene, Ap3b2, is a neuron-specific gene and is involved in the formation of synaptic vesicles, transfer of membrane proteins to lysosomes, and endocytosis (42, 43).”
Background
- Authors
- Blumstein, J., Faundez, V., Nakatsu, F., Saito, T., Ohno, H., & Kelly, R. B.
- Affiliations
- University of California, San Francisco (US)
- Kanazawa University (JP)
- Chiba University (JP)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2001-10-15
- Volume
- 21
- Issue
- 20
- Pages
- 8034-8042
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6763874
- OpenAlex
- W2163046615
- Cited by
- 98
- References
- 1
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 4 · 2023: 4 · 2022: 3 · 2021: 1 · 2020: 3 · 2019: 2 · 2018: 2 · 2017: 3 · 2016: 3 · 2015: 5 · 2014: 3 · 2013: 5 · 2012: 8
- FWCI
- 2.16
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Uehara Memorial Foundation
- National Institutes of Health (5r01ns009878-31, NS09878, DA10154)
- National Institute on Drug Abuse (P01DA010154, DA-10154)
- National Institute of Neurological Disorders and Stroke (NS 09878)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- synaptic vesicle formation, endosomes, vesicle formation, clathrin-mediated endocytosis, AP-2, axons, varicosities, neurological disorders, GTP gamma S
- MeSH terms
- Adenosine Triphosphate, Animals, Antibodies, Axons, Brain, Brain Chemistry, Carrier Proteins, Cell Line, Cell-Free System, Cytosol, Female, Humans, Membrane Proteins, Mice, Mutant Strains, Neurons, Organ Specificity, Endosomes, Synaptic Vesicles, Guanosine 5'-O-(3-Thiotriphosphate), PC12 Cells, Rats, Sprague-Dawley, Protein Isoforms, Adaptor Proteins, Vesicular Transport, Monomeric Clathrin Assembly Proteins, R-SNARE Proteins, Mice, Rats
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