Synaptic Vesicle Generation from Central Nerve Terminal Endosomes
Central nerve terminals contain a small number of synaptic vesicles (SVs) that must sustain the fidelity of neurotransmission across a wide range of stimulation intensities. For this to be achieved, nerve terminals integrate a number of complementary endocytosis modes whose activation spans the brea...
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Veröffentlicht in: | Traffic (Copenhagen, Denmark) Denmark), 2015-03, Vol.16 (3), p.229-240 |
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description | Central nerve terminals contain a small number of synaptic vesicles (SVs) that must sustain the fidelity of neurotransmission across a wide range of stimulation intensities. For this to be achieved, nerve terminals integrate a number of complementary endocytosis modes whose activation spans the breadth of these neuronal stimulation patterns. Two such modes are ultrafast endocytosis and activity‐dependent bulk endocytosis, which are triggered by stimuli at either end of the physiological range. Both endocytosis modes generate endosomes directly from the nerve terminal plasma membrane, before the subsequent production of SVs from these structures. This review will discuss the current knowledge relating to the molecular mechanisms involved in the generation of SVs from nerve terminal endosomes, how this relates to other mechanisms of SV production and the functional role of such SVs.
Studies investigating the direct generation of endosomes during endocytosis in central nerve terminals have enjoyed a renaissance in the past 5 years. However, relatively little is known regarding the molecular basis of subsequent synaptic vesicle (SV) generation from these endosomes. This article discusses potential mechanisms and how endosome‐derived SVs contribute to central nerve terminal function. |
doi_str_mv | 10.1111/tra.12235 |
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Studies investigating the direct generation of endosomes during endocytosis in central nerve terminals have enjoyed a renaissance in the past 5 years. However, relatively little is known regarding the molecular basis of subsequent synaptic vesicle (SV) generation from these endosomes. This article discusses potential mechanisms and how endosome‐derived SVs contribute to central nerve terminal function.</description><identifier>ISSN: 1398-9219</identifier><identifier>EISSN: 1600-0854</identifier><identifier>DOI: 10.1111/tra.12235</identifier><identifier>PMID: 25346420</identifier><language>eng</language><publisher>Former Munksgaard: John Wiley & Sons A/S</publisher><subject>Animals ; Cell Membrane - physiology ; Central Nervous System - physiology ; clathrin ; dynamin ; Endocytosis ; Endocytosis - physiology ; endosome ; Endosomes - physiology ; Nerve Endings - physiology ; presynapse ; Synaptic Vesicles - physiology ; vesicle</subject><ispartof>Traffic (Copenhagen, Denmark), 2015-03, Vol.16 (3), p.229-240</ispartof><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4195-19c524df217f6ba21814122a63780d8b4fd609dfe0be3e9c49f9e713984f9e13</citedby><cites>FETCH-LOGICAL-c4195-19c524df217f6ba21814122a63780d8b4fd609dfe0be3e9c49f9e713984f9e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftra.12235$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftra.12235$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25346420$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kokotos, Alexandros C.</creatorcontrib><creatorcontrib>Cousin, Michael A.</creatorcontrib><title>Synaptic Vesicle Generation from Central Nerve Terminal Endosomes</title><title>Traffic (Copenhagen, Denmark)</title><addtitle>Traffic</addtitle><description>Central nerve terminals contain a small number of synaptic vesicles (SVs) that must sustain the fidelity of neurotransmission across a wide range of stimulation intensities. For this to be achieved, nerve terminals integrate a number of complementary endocytosis modes whose activation spans the breadth of these neuronal stimulation patterns. Two such modes are ultrafast endocytosis and activity‐dependent bulk endocytosis, which are triggered by stimuli at either end of the physiological range. Both endocytosis modes generate endosomes directly from the nerve terminal plasma membrane, before the subsequent production of SVs from these structures. This review will discuss the current knowledge relating to the molecular mechanisms involved in the generation of SVs from nerve terminal endosomes, how this relates to other mechanisms of SV production and the functional role of such SVs.
Studies investigating the direct generation of endosomes during endocytosis in central nerve terminals have enjoyed a renaissance in the past 5 years. However, relatively little is known regarding the molecular basis of subsequent synaptic vesicle (SV) generation from these endosomes. This article discusses potential mechanisms and how endosome‐derived SVs contribute to central nerve terminal function.</description><subject>Animals</subject><subject>Cell Membrane - physiology</subject><subject>Central Nervous System - physiology</subject><subject>clathrin</subject><subject>dynamin</subject><subject>Endocytosis</subject><subject>Endocytosis - physiology</subject><subject>endosome</subject><subject>Endosomes - physiology</subject><subject>Nerve Endings - physiology</subject><subject>presynapse</subject><subject>Synaptic Vesicles - physiology</subject><subject>vesicle</subject><issn>1398-9219</issn><issn>1600-0854</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFLwzAYhoMobk4P_gEpeNFDtyRNs-Y4xpzCUNDiNaTtF-hom5m0Sv-92To9COaS74OHh-99EbomeEr8m7VWTQmlUXyCxoRjHOIkZqd-jkQSCkrECF04t8UY05ixczSiccQ4o3iMFm99o3ZtmQfv4Mq8gmANDVjVlqYJtDV1sITG-6vgGewnBCnYumz8umoK40wN7hKdaVU5uDr-E5Q-rNLlY7h5WT8tF5swZ0TEIRF5TFmhKZlrnilKEsL8zYpH8wQXScZ0wbEoNOAMIhA5E1rAfJ-A-YFEE3Q3aHfWfHTgWlmXLoeqUg2YzknC48QnIj7aBN3-Qbems_7oA8VpxAVOPHU_ULk1zlnQcmfLWtleEiz3tUofWx5q9ezN0dhlNRS_5E-PHpgNwFdZQf-_Saavi0H5DYAwf2I</recordid><startdate>201503</startdate><enddate>201503</enddate><creator>Kokotos, Alexandros C.</creator><creator>Cousin, Michael A.</creator><general>John Wiley & Sons A/S</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201503</creationdate><title>Synaptic Vesicle Generation from Central Nerve Terminal Endosomes</title><author>Kokotos, Alexandros C. ; Cousin, Michael A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4195-19c524df217f6ba21814122a63780d8b4fd609dfe0be3e9c49f9e713984f9e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Cell Membrane - physiology</topic><topic>Central Nervous System - physiology</topic><topic>clathrin</topic><topic>dynamin</topic><topic>Endocytosis</topic><topic>Endocytosis - physiology</topic><topic>endosome</topic><topic>Endosomes - physiology</topic><topic>Nerve Endings - physiology</topic><topic>presynapse</topic><topic>Synaptic Vesicles - physiology</topic><topic>vesicle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kokotos, Alexandros C.</creatorcontrib><creatorcontrib>Cousin, Michael A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Traffic (Copenhagen, Denmark)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kokotos, Alexandros C.</au><au>Cousin, Michael A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synaptic Vesicle Generation from Central Nerve Terminal Endosomes</atitle><jtitle>Traffic (Copenhagen, Denmark)</jtitle><addtitle>Traffic</addtitle><date>2015-03</date><risdate>2015</risdate><volume>16</volume><issue>3</issue><spage>229</spage><epage>240</epage><pages>229-240</pages><issn>1398-9219</issn><eissn>1600-0854</eissn><abstract>Central nerve terminals contain a small number of synaptic vesicles (SVs) that must sustain the fidelity of neurotransmission across a wide range of stimulation intensities. For this to be achieved, nerve terminals integrate a number of complementary endocytosis modes whose activation spans the breadth of these neuronal stimulation patterns. Two such modes are ultrafast endocytosis and activity‐dependent bulk endocytosis, which are triggered by stimuli at either end of the physiological range. Both endocytosis modes generate endosomes directly from the nerve terminal plasma membrane, before the subsequent production of SVs from these structures. This review will discuss the current knowledge relating to the molecular mechanisms involved in the generation of SVs from nerve terminal endosomes, how this relates to other mechanisms of SV production and the functional role of such SVs.
Studies investigating the direct generation of endosomes during endocytosis in central nerve terminals have enjoyed a renaissance in the past 5 years. However, relatively little is known regarding the molecular basis of subsequent synaptic vesicle (SV) generation from these endosomes. This article discusses potential mechanisms and how endosome‐derived SVs contribute to central nerve terminal function.</abstract><cop>Former Munksgaard</cop><pub>John Wiley & Sons A/S</pub><pmid>25346420</pmid><doi>10.1111/tra.12235</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Cell Membrane - physiology Central Nervous System - physiology clathrin dynamin Endocytosis Endocytosis - physiology endosome Endosomes - physiology Nerve Endings - physiology presynapse Synaptic Vesicles - physiology vesicle |
title | Synaptic Vesicle Generation from Central Nerve Terminal Endosomes |
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