The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
Cholesterol reduction impairs exocytosis of synaptic vesicles
Open accessAbstract
Cholesterol and sphingolipids are abundant in neuronal membranes, where they help the organisation of the membrane microdomains involved in major roles such as axonal and dendritic growth, and synapse and spine stability. The aim of this study was to analyse their roles in presynaptic physiology. We first confirmed the presence of proteins of the exocytic machinery (SNARES and Ca(v)2.1 channels) in the lipid microdomains of cultured neurons, and then incubated the neurons with fumonisin B (an inhibitor of sphingolipid synthesis), or with mevastatin or zaragozic acid (two compounds that affect the synthesis of cholesterol by inhibiting HMG-CoA reductase or squalene synthase). The results demonstrate that fumonisin B and zaragozic acid efficiently decrease sphingolipid and cholesterol levels without greatly affecting the viability of neurons or the expression of synaptic proteins. Electron microscopy showed that the morphology and number of synaptic vesicles in the presynaptic boutons of cholesterol-depleted neurons were similar to those observed in control neurons. Zaragozic acid (but not fumonisin B) treatment impaired synaptic vesicle uptake of the lipophilic dye FM1-43 and an antibody directed against the luminal epitope of synaptotagmin-1, effects that depended on the reduction in cholesterol because they were reversed by cholesterol reloading. The time-lapse confocal imaging of neurons transfected with ecliptic SynaptopHluorin showed that cholesterol depletion affects the…
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“One mechanism that might contribute to these effects is the restoration of membrane lipid rafts, cholesterol-enriched microdomains that organize signaling molecules and synaptic proteins and are required for efficient synaptic transmission (Korinek et al., 2020;Linetti et al., 2010).”
From Impaired astrocyte-to-neuron cholesterol trafficking drives synaptic dysfunction in Rett syndrome (2026) · cites this paper as Linetti et al., 2010
In the citing paper
“Cholesterol is essential for neurons, because a lack of cholesterol leads to synapse degeneration, impaired synaptic vesicle exocytosis and neurotransmission, and overall decreased neuronal activity.[42][43][44]”
From Canonical Wnt pathway and the LDL receptor superfamily in neuronal cholesterol homeostasis and function (2024) · cites this paper as [43]
In the citing paper
“These findings also suggest that within the striatum, the astrocyte-neuron signaling may be synapse-and cell-specific by acting at least on the DRD2-MSNs, as recently proposed 53 .”
From SREBP2 gene therapy targeting striatal astrocytes ameliorates Huntington’s disease phenotypes (2021) · cites this paper as [53]
Citations
Cites
Functional rafts in cell membranes
Simons, K., & Ikonen, E. (1997) · Nature · doi:10.1038/42408 · Cited by 9,757 · cited 4×
“…in neurons in order to distinguish the proteins associated with lipid or non-lipid microdomains on the basis of the operational definition of lipid microdomains as membrane regions that are insoluble in cold anionic detergents (Simons and Ikonen, 1997; Brown and London, 1998; Hering et al., 2003).”
BackgroundMethodInfluentialFunctions of lipid rafts in biological membranes.
Brown, D. A., & London, E. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.111 · Cited by 3,027
Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins
Miesenböck, G., Angelis, D. A. D., & Rothman, J. E. (1998) · Nature · doi:10.1038/28190 · Cited by 2,569
Wilschut, J. (1990) · Cited by 2,407
Molecular anatomy of a trafficking organelle
Takamori, S., Holt, M., Stenius, K., Lemke, E. A., Grønborg, M., Riedel, D., Urlaub, H., Schenck, S., Brügger, B., Ringler, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.10.030 · Cited by 2,373
Structure and Regulation of Voltage-Gated Ca 2+ Channels
Catterall, W. A. (2000) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.16.1.521 · Cited by 2,344
Model Systems, Lipid Rafts, and Cell Membranes
Simons, K., & Vaz, W. L. C. (2004) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.32.110601.141803 · Cited by 1,695
Rafts defined: a report on the Keystone symposium on lipid rafts and cell function
PIKE, L. J. (2006) · Journal of Lipid Research · doi:10.1194/jlr.e600002-jlr200 · Cited by 1,500
Jahn, R., Lang, T., & Südhof, T. C. (2003) · Cell · doi:10.1016/s0092-8674(03)00112-0 · Cited by 1,364
Cholesterol depletion inhibits the generation of β-amyloid in hippocampal neurons
Simons, M., Keller, P., Strooper, B. D., Beyreuther, K. T., Dotti, C. G., & Simons, K. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6460 · Cited by 1,177
Zidovetzki, R., & Levitan, I. (2007) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2007.03.026 · Cited by 1,141
Definition of the readily releasable pool of vesicles at hippocampal synapses.
Rosenmund, C., & Stevens, C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80146-4 · Cited by 1,084
Lipid raft microdomains and neurotransmitter signalling
Allen, J., Halverson-Tamboli, R. A., & Rasenick, M. M. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn2059 · Cited by 880
Optical Analysis of Synaptic Vesicle Recycling at the Frog Neuromuscular Junction
Betz, W. J., & Bewick, G. S. (1992) · Science · doi:10.1126/science.1553547 · Cited by 763
Lipid rafts: heterogeneity on the high seas
PIKE, L. J. (2004) · Biochemical Journal · doi:10.1042/bj20031672 · Cited by 705
Lang, T., Bruns, D., Wenzel, D., Riedel, D., Holroyd, P., Thiele, C., & Jahn, R. (2001) · The EMBO Journal · doi:10.1093/emboj/20.9.2202 · Cited by 686
Subunit-specific temporal and spatial patterns of AMPA receptor exocytosis in hippocampal neurons
Passafaro, M., Piëch, V., & Sheng, M. (2001) · Nature Neuroscience · doi:10.1038/nn0901-917 · Cited by 655
Self-citationLipid Rafts in the Maintenance of Synapses, Dendritic Spines, and Surface AMPA Receptor Stability
Hering, H., Lin, C.-C., & Sheng, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03262.2003 · Cited by 622
Cholesterol binds to synaptophysin and is required for biogenesis of synaptic vesicles
Thiele, C., Hannah, M. J., Fahrenholz, F., & Huttner, W. B. (2000) · Nature Cell Biology · doi:10.1038/71366 · Cited by 498
Klein, U., Gimpl, G., & Fahrenholz, F. (1995) · Biochemistry · doi:10.1021/bi00042a009 · Cited by 481
Chamberlain, L. H., Burgoyne, R. D., & Gould, G. W. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091502398 · Cited by 432
Lipid rafts in neuronal signaling and function.
Tsui-Pierchala, B. A., Encinas, M., Milbrandt, J., & Johnson, E. M. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02215-4 · Cited by 420
Rho GTPases, dendritic structure, and mental retardation
Newey, S. E., Velamoor, V., Govek, E., & Van Aelst, L. (2005) · Journal of Neurobiology · doi:10.1002/neu.20153 · Cited by 351
Three-Dimensional Architecture of Presynaptic Terminal Cytomatrix
Siksou, L., Rostaing, P., Lechaire, J., Boudier, T., Ohtsuka, T., Fejtová, A., Kao, H., Greengard, P., Gundelfinger, E. D., Triller, A., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1773-07.2007 · Cited by 340
Bergstrom, J. D., Kurtz, M. M., Rew, D. J., Amend, A. M., Karkas, J. D., Bostedor, R., Bansal, V. S., Dufresne, C., VanMiddlesworth, F. L., & Hensens, O. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.1.80 · Cited by 335
Matteoli, M., Takei, K., Perin, M., Südhof, T., & Camilli, P. D. (1992) · Journal of Cell Biology · doi:10.1083/jcb.117.4.849 · Cited by 326
Self-citationInduction of dendritic spines by an extracellular domain of AMPA receptor subunit GluR2
Passafaro, M., Nakagawa, T., Sala, C., & Sheng, M. (2003) · Nature · doi:10.1038/nature01781 · Cited by 306
Self-citationLipid Rafts and the Regulation of Exocytosis
Salaün, C., James, D. J., & Chamberlain, L. H. (2004) · Traffic · doi:10.1111/j.1600-0854.2004.0162.x · Cited by 301
Effects of membrane lipids on ion channel structure and function
Tillman, T. S., & Cascio, M. (2003) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:38:2:161 · Cited by 265
Molecular determinants of presynaptic active zones
Garner, C. C., Kindler, S., & Gundelfinger, E. D. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00093-3 · Cited by 221
Neuronal polarity: Essential role of protein–lipid complexes in axonal sorting
Ledesma, M. D., Simons, K., & Dotti, C. G. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3966 · Cited by 219
Rab proteins in regulated exocytosis
von Mollard, G. F., Stahl, B., Li, C., Südhof, T. C., & Jahn, R. (1994) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(94)90278-x · Cited by 197
Cholesterol facilitates the native mechanism of Ca2+-triggered membrane fusion
Churchward, M. A., Rogasevskaia, T. P., Höfgen, J., Bau, J. T., & Coorssen, J. R. (2005) · Journal of Cell Science · doi:10.1242/jcs.02601 · Cited by 178
Churchward, M. A., Rogasevskaia, T. P., Brandman, D. M., Khosravani, H., Nava, P., Atkinson, J. K., & Coorssen, J. R. (2008) · Biophysical Journal · doi:10.1529/biophysj.107.123984 · Cited by 159
Sphingosine Facilitates SNARE Complex Assembly and Activates Synaptic Vesicle Exocytosis
Darios, F., Wasser, C. R., Shakirzyanova, A., Giniatullin, A., Goodman, K., Muñoz-Bravo, J. L., Raingo, J., Jorgačevski, J., Kreft, M., Zorec, R., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.024 · Cited by 157
Golub, T., & Caroni, P. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200407058 · Cited by 154
Cholesterol‐dependent balance between evoked and spontaneous synaptic vesicle recycling
Wasser, C. R., Ertunç, M., Liu, X., & Kavalali, E. T. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.123133 · Cited by 150
SNARE-Mediated Lipid Mixing Depends on the Physical State of the Vesicles
Chen, X., Araç, D., Wang, T.-M., Gilpin, C. J., Zimmerberg, J. J., & Rizo, J. (2005) · Biophysical Journal · doi:10.1529/biophysj.105.071415 · Cited by 142
Taverna, E., Saba, E., Rowe, J., Francolini, M., Clementi, F., & Rosa, P. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m308798200 · Cited by 139
Self-citationLipid raft heterogeneity: an enigma
Mishra, S., & Joshi, P. G. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04720.x · Cited by 117
A scissors mechanism for stimulation of SNARE-mediated lipid mixing by cholesterol
Tong, J., Borbat, P. P., Freed, J. H., & Shin, Y. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813138106 · Cited by 111
Ceramidase Regulates Synaptic Vesicle Exocytosis and Trafficking
Rohrbough, J. C., Rushton, E., Musselman, L. P., Woodruff, E. A., Matthies, H. J. G., Acharya, U. R., Acharya, J., & Broadie, K. S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1146-04.2004 · Cited by 104
Schulz, J. G., Bösel, J., Stoeckel, M., Megow, D., Dirnagl, U., & Endres, M. (2004) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02305.x · Cited by 104
Cholesterol effects on nicotinic acetylcholine receptor
Barrantes, F. J. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04719.x · Cited by 99
Cholesterol and lipid microdomains stabilize the postsynapse at the neuromuscular junction
Willmann, R., Pun, S., Stallmach, L., Sadasivam, G., Santos, A. F., Caroni, P., & Fuhrer, C. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601288 · Cited by 99
The region‐specific activities of lipid rafts during axon growth and guidance
Kamiguchi, H. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03888.x · Cited by 98
Cholesterol and synaptic transmitter release at crayfish neuromuscular junctions
Zamir, O., & Charlton, M. P. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.098319 · Cited by 97
Pechlivanis, M., & Kuhlmann, J. (2006) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2006.09.017 · Cited by 92
Repko, E. M., & Maltese, W. A. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)81751-3 · Cited by 90
Rowe, J., Calegari, F., Taverna, E., Longhi, R., & Rosa, P. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.18.3323 · Cited by 89
Self-citationQuantitative Proteomics Analysis of Detergent-resistant Membranes from Chemical Synapses
Jia, J.-Y., Lamer, S., Schümann, M., Schmidt, M. R., Krause, E., & Haucke, V. (2006) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m600161-mcp200 · Cited by 73
Vesicle turnover in developing neurons: how to build a presynaptic terminal
Matteoli, M. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.01.007 · Cited by 43
Self-citationLocalization of synaptic proteins involved in neurosecretion in different membrane microdomains
Taverna, E., Saba, E., Linetti, A., Longhi, R., Jeromin, A., Righi, M., Clementi, F., & Rosa, P. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04225.x · Cited by 34
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Metadata
- Authors
- Linetti, A., Fratangeli, A., Taverna, E., Valnegri, P., Francolini, M., Cappello, V., Matteoli, M., Passafaro, M., & Rosa, P.
- Affiliations
- University of Milan (IT)
- Corresponding author
- Rosa, Patrizia
- ORCID
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2010-02-15
- Volume
- 123
- Issue
- 4
- Pages
- 595-605
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W2160339294
- Cited by
- 209
- References
- 53
- Citations by year
- 2026: 6 · 2025: 16 · 2024: 13 · 2023: 14 · 2022: 15 · 2021: 12 · 2020: 17 · 2019: 15 · 2018: 13 · 2017: 11 · 2016: 11 · 2015: 14 · 2014: 19 · 2013: 16 · 2012: 5
- FWCI
- 4.61
- Type
- journal article
- Language
- en
- Open access
- green
- zenodo.org
- Licence
- cc-by
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed (publishedVersion)
- INFM-OAR (INFN Catania) (submittedVersion, cc-by)
- Funders
- Compagnia di San Paolo (2005.1964)
- Università degli Studi di Milano
- Fondazione Cariplo
- Ministero dell’Istruzione, dell’Università e della Ricerca
- Consiglio Nazionale delle Ricerche
- Università degli Studi di Genova
- 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 › Lipid Membrane Structure and Behavior
- Keywords
- cholesterol, sphingolipids, synaptic vesicle exocytosis, presynaptic terminals, lipid rafts, fumonisin B, zaragozic acid, mevastatin, HMG-CoA reductase inhibition, squalene synthase inhibition, SNARE proteins, synaptotagmin-1, cholesterol depletion
- MeSH terms
- Animals, Anticholesteremic Agents, Cells, Cultured, Cholesterol, Exocytosis, Immunoglobulin G, Lovastatin, Models, Neurological, Neurons, Sphingolipids, Synaptic Vesicles, Tricarboxylic Acids, Presynaptic Terminals, Bridged Bicyclo Compounds, Heterocyclic, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Calcium Channels, N-Type, Membrane Microdomains, Fumonisins, Microscopy, Electron, Transmission, SNARE Proteins, Synaptotagmin I, Rats
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