Synapses, spines and kinases in mammalian learning and memory, and the impact of aging
Synapses are the building blocks of neuronal networks. Spines, the postsynaptic elements, are morphologically the most plastic part of the synapse. It is thought that spine plasticity underlies learning and memory processes, driven by kinases and cytoskeleton protein reorganization. Spine strength d...
Gespeichert in:
Veröffentlicht in: | Neuroscience and biobehavioral reviews 2015-03, Vol.50, p.77-85 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 85 |
---|---|
container_issue | |
container_start_page | 77 |
container_title | Neuroscience and biobehavioral reviews |
container_volume | 50 |
creator | van der Zee, Eddy A |
description | Synapses are the building blocks of neuronal networks. Spines, the postsynaptic elements, are morphologically the most plastic part of the synapse. It is thought that spine plasticity underlies learning and memory processes, driven by kinases and cytoskeleton protein reorganization. Spine strength depends primarily on the number of incorporated glutamatergic receptors, which are more numerous in larger spines. Intrinsic and circadian fluctuations, occurring independently of presynaptic stimulation, demonstrate the native instability of spines. Despite innate spine instability some spines remain intact lifelong. Threats to spine survival are reduced by physical and mental activity, and declining sensory input, conditions characteristic for aging. Large spines are considered less vulnerable than thin spines, and in the older brain large spines are more abundant, whereas the thin spines are functionally weaker. It can be speculated that this shift towards memory spines contributes to enhanced retention of remote memories typically seen in the elderly. Gaining further insight in spine plasticity regulation, its homeostatic nature and how to maintain spine health will be important future research topics in Neuroscience. |
doi_str_mv | 10.1016/j.neubiorev.2014.06.012 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1675871721</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1675871721</sourcerecordid><originalsourceid>FETCH-LOGICAL-c395t-9cebb3502a37c23fce4d3006d269000fc83fe0879ff1a1dad19611f746377dbe3</originalsourceid><addsrcrecordid>eNo9kMlOwzAQQC0EoqXwC-AjhyZ4SezkiCo2qRIHlqvlJOPiEjshTpD696QLPc1o5s2ih9ANJTElVNytYw9DYZsOfmNGaBITERPKTtCUZpJHMmXZKZqOjTySgicTdBHCmhDCCE_P0YQleZ4lJJuiz7eN122AMMehtR4C1r7C39brsYatx047p2urPa5Bd9761Y5w4JpuM9_l_Rdg61pd9rgxWK9G5hKdGV0HuDrEGfp4fHhfPEfL16eXxf0yKnme9lFeQlHwlDDNZcm4KSGpOCGiYiIfvzVlxg2QTObGUE0rXdFcUGpkIriUVQF8hm73e9uu-Rkg9MrZUEJdaw_NEBQVMs0klYyOqNyjZdeE0IFRbWed7jaKErWVqtbqKFVtpSoi1Ch1nLw-HBkKB9Vx7t8i_wONQXZg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1675871721</pqid></control><display><type>article</type><title>Synapses, spines and kinases in mammalian learning and memory, and the impact of aging</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>van der Zee, Eddy A</creator><creatorcontrib>van der Zee, Eddy A</creatorcontrib><description>Synapses are the building blocks of neuronal networks. Spines, the postsynaptic elements, are morphologically the most plastic part of the synapse. It is thought that spine plasticity underlies learning and memory processes, driven by kinases and cytoskeleton protein reorganization. Spine strength depends primarily on the number of incorporated glutamatergic receptors, which are more numerous in larger spines. Intrinsic and circadian fluctuations, occurring independently of presynaptic stimulation, demonstrate the native instability of spines. Despite innate spine instability some spines remain intact lifelong. Threats to spine survival are reduced by physical and mental activity, and declining sensory input, conditions characteristic for aging. Large spines are considered less vulnerable than thin spines, and in the older brain large spines are more abundant, whereas the thin spines are functionally weaker. It can be speculated that this shift towards memory spines contributes to enhanced retention of remote memories typically seen in the elderly. Gaining further insight in spine plasticity regulation, its homeostatic nature and how to maintain spine health will be important future research topics in Neuroscience.</description><identifier>ISSN: 0149-7634</identifier><identifier>EISSN: 1873-7528</identifier><identifier>DOI: 10.1016/j.neubiorev.2014.06.012</identifier><identifier>PMID: 24998408</identifier><language>eng</language><publisher>United States</publisher><subject>Aging ; Animals ; Brain - enzymology ; Brain - physiology ; Dendritic Spines - enzymology ; Humans ; Learning - physiology ; Mammals ; Memory - physiology ; Neuronal Plasticity ; Phosphotransferases - physiology ; Synapses - enzymology</subject><ispartof>Neuroscience and biobehavioral reviews, 2015-03, Vol.50, p.77-85</ispartof><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-9cebb3502a37c23fce4d3006d269000fc83fe0879ff1a1dad19611f746377dbe3</citedby><cites>FETCH-LOGICAL-c395t-9cebb3502a37c23fce4d3006d269000fc83fe0879ff1a1dad19611f746377dbe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24998408$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Zee, Eddy A</creatorcontrib><title>Synapses, spines and kinases in mammalian learning and memory, and the impact of aging</title><title>Neuroscience and biobehavioral reviews</title><addtitle>Neurosci Biobehav Rev</addtitle><description>Synapses are the building blocks of neuronal networks. Spines, the postsynaptic elements, are morphologically the most plastic part of the synapse. It is thought that spine plasticity underlies learning and memory processes, driven by kinases and cytoskeleton protein reorganization. Spine strength depends primarily on the number of incorporated glutamatergic receptors, which are more numerous in larger spines. Intrinsic and circadian fluctuations, occurring independently of presynaptic stimulation, demonstrate the native instability of spines. Despite innate spine instability some spines remain intact lifelong. Threats to spine survival are reduced by physical and mental activity, and declining sensory input, conditions characteristic for aging. Large spines are considered less vulnerable than thin spines, and in the older brain large spines are more abundant, whereas the thin spines are functionally weaker. It can be speculated that this shift towards memory spines contributes to enhanced retention of remote memories typically seen in the elderly. Gaining further insight in spine plasticity regulation, its homeostatic nature and how to maintain spine health will be important future research topics in Neuroscience.</description><subject>Aging</subject><subject>Animals</subject><subject>Brain - enzymology</subject><subject>Brain - physiology</subject><subject>Dendritic Spines - enzymology</subject><subject>Humans</subject><subject>Learning - physiology</subject><subject>Mammals</subject><subject>Memory - physiology</subject><subject>Neuronal Plasticity</subject><subject>Phosphotransferases - physiology</subject><subject>Synapses - enzymology</subject><issn>0149-7634</issn><issn>1873-7528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMlOwzAQQC0EoqXwC-AjhyZ4SezkiCo2qRIHlqvlJOPiEjshTpD696QLPc1o5s2ih9ANJTElVNytYw9DYZsOfmNGaBITERPKTtCUZpJHMmXZKZqOjTySgicTdBHCmhDCCE_P0YQleZ4lJJuiz7eN122AMMehtR4C1r7C39brsYatx047p2urPa5Bd9761Y5w4JpuM9_l_Rdg61pd9rgxWK9G5hKdGV0HuDrEGfp4fHhfPEfL16eXxf0yKnme9lFeQlHwlDDNZcm4KSGpOCGiYiIfvzVlxg2QTObGUE0rXdFcUGpkIriUVQF8hm73e9uu-Rkg9MrZUEJdaw_NEBQVMs0klYyOqNyjZdeE0IFRbWed7jaKErWVqtbqKFVtpSoi1Ch1nLw-HBkKB9Vx7t8i_wONQXZg</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>van der Zee, Eddy A</creator><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>7X8</scope></search><sort><creationdate>20150301</creationdate><title>Synapses, spines and kinases in mammalian learning and memory, and the impact of aging</title><author>van der Zee, Eddy A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-9cebb3502a37c23fce4d3006d269000fc83fe0879ff1a1dad19611f746377dbe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aging</topic><topic>Animals</topic><topic>Brain - enzymology</topic><topic>Brain - physiology</topic><topic>Dendritic Spines - enzymology</topic><topic>Humans</topic><topic>Learning - physiology</topic><topic>Mammals</topic><topic>Memory - physiology</topic><topic>Neuronal Plasticity</topic><topic>Phosphotransferases - physiology</topic><topic>Synapses - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Zee, Eddy 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>MEDLINE - Academic</collection><jtitle>Neuroscience and biobehavioral reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Zee, Eddy A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synapses, spines and kinases in mammalian learning and memory, and the impact of aging</atitle><jtitle>Neuroscience and biobehavioral reviews</jtitle><addtitle>Neurosci Biobehav Rev</addtitle><date>2015-03-01</date><risdate>2015</risdate><volume>50</volume><spage>77</spage><epage>85</epage><pages>77-85</pages><issn>0149-7634</issn><eissn>1873-7528</eissn><abstract>Synapses are the building blocks of neuronal networks. Spines, the postsynaptic elements, are morphologically the most plastic part of the synapse. It is thought that spine plasticity underlies learning and memory processes, driven by kinases and cytoskeleton protein reorganization. Spine strength depends primarily on the number of incorporated glutamatergic receptors, which are more numerous in larger spines. Intrinsic and circadian fluctuations, occurring independently of presynaptic stimulation, demonstrate the native instability of spines. Despite innate spine instability some spines remain intact lifelong. Threats to spine survival are reduced by physical and mental activity, and declining sensory input, conditions characteristic for aging. Large spines are considered less vulnerable than thin spines, and in the older brain large spines are more abundant, whereas the thin spines are functionally weaker. It can be speculated that this shift towards memory spines contributes to enhanced retention of remote memories typically seen in the elderly. Gaining further insight in spine plasticity regulation, its homeostatic nature and how to maintain spine health will be important future research topics in Neuroscience.</abstract><cop>United States</cop><pmid>24998408</pmid><doi>10.1016/j.neubiorev.2014.06.012</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0149-7634 |
ispartof | Neuroscience and biobehavioral reviews, 2015-03, Vol.50, p.77-85 |
issn | 0149-7634 1873-7528 |
language | eng |
recordid | cdi_proquest_miscellaneous_1675871721 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Aging Animals Brain - enzymology Brain - physiology Dendritic Spines - enzymology Humans Learning - physiology Mammals Memory - physiology Neuronal Plasticity Phosphotransferases - physiology Synapses - enzymology |
title | Synapses, spines and kinases in mammalian learning and memory, and the impact of aging |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T01%3A42%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synapses,%20spines%20and%20kinases%20in%20mammalian%20learning%20and%20memory,%20and%20the%20impact%20of%20aging&rft.jtitle=Neuroscience%20and%20biobehavioral%20reviews&rft.au=van%20der%20Zee,%20Eddy%20A&rft.date=2015-03-01&rft.volume=50&rft.spage=77&rft.epage=85&rft.pages=77-85&rft.issn=0149-7634&rft.eissn=1873-7528&rft_id=info:doi/10.1016/j.neubiorev.2014.06.012&rft_dat=%3Cproquest_cross%3E1675871721%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1675871721&rft_id=info:pmid/24998408&rfr_iscdi=true |