Loading…

Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins

Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusi...

Full description

Saved in:
Bibliographic Details
Published in:Neurochemistry international 2006-08, Vol.49 (3), p.270-275
Main Authors: Trikash, I.O., Kolchinskaya, L.I.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853
cites cdi_FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853
container_end_page 275
container_issue 3
container_start_page 270
container_title Neurochemistry international
container_volume 49
creator Trikash, I.O.
Kolchinskaya, L.I.
description Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca 2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca 2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.
doi_str_mv 10.1016/j.neuint.2006.01.014
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68627818</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0197018606000830</els_id><sourcerecordid>68627818</sourcerecordid><originalsourceid>FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</originalsourceid><addsrcrecordid>eNqFkUGLFDEQhYMo7uzqPxDJRW89pjLpJH0RZHFdYcGLnmM6XY0Z0snY1b2w_34zzMDcFArq8r1XxXuMvQOxBQH6036bcY152Uoh9FZAHfWCbcAa2XSmVS_ZRkBnGgFWX7Fror0QwnSifc2uQLcWoNUb9vtupVgyLyOnp-wPSwz8ESmGhMR9HvgheZo8n3DqZ5-Rx8yXP8gPMxLmgBdhoTL5xKmktU9HoCwYM71hr0afCN-e9w37dff15-198_Dj2_fbLw9NUBKWRhoFdthZiVZZDQPAOHZ6FzwOaLS3IrS69RZ6bUeQ3lSkFwP0KGzQYNvdDft48q2H_65Ii5siBUypPl1WctpqaSzY_4JgpFJG7SqoTmCYC9GMozvMcfLzkwPhjhW4vTtV4I4VOAF1VJW9P_uv_YTDRXTOvAIfzoCn4NNYYw2RLpzplNIgK_f5xGGN7THi7CjEY-ZDnDEsbijx3588A-3Ap0k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17244743</pqid></control><display><type>article</type><title>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</title><source>ScienceDirect Journals</source><creator>Trikash, I.O. ; Kolchinskaya, L.I.</creator><creatorcontrib>Trikash, I.O. ; Kolchinskaya, L.I.</creatorcontrib><description>Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca 2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca 2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</description><identifier>ISSN: 0197-0186</identifier><identifier>EISSN: 1872-9754</identifier><identifier>DOI: 10.1016/j.neuint.2006.01.014</identifier><identifier>PMID: 16581156</identifier><identifier>CODEN: NEUIDS</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; Cell Membrane - metabolism ; Cell-free model system ; Exocytosis ; Fundamental and applied biological sciences. Psychology ; Membrane fusion ; Membrane Fusion - physiology ; Membrane Proteins - metabolism ; Rats ; Rats, Wistar ; SNARE proteins ; SNARE Proteins - metabolism ; Solubility ; Synaptic Membranes - metabolism ; Synaptic Vesicles - metabolism ; Synaptosomes - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Neurochemistry international, 2006-08, Vol.49 (3), p.270-275</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</citedby><cites>FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17944612$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16581156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trikash, I.O.</creatorcontrib><creatorcontrib>Kolchinskaya, L.I.</creatorcontrib><title>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</title><title>Neurochemistry international</title><addtitle>Neurochem Int</addtitle><description>Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca 2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca 2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Membrane - metabolism</subject><subject>Cell-free model system</subject><subject>Exocytosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Membrane fusion</subject><subject>Membrane Fusion - physiology</subject><subject>Membrane Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>SNARE proteins</subject><subject>SNARE Proteins - metabolism</subject><subject>Solubility</subject><subject>Synaptic Membranes - metabolism</subject><subject>Synaptic Vesicles - metabolism</subject><subject>Synaptosomes - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0197-0186</issn><issn>1872-9754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkUGLFDEQhYMo7uzqPxDJRW89pjLpJH0RZHFdYcGLnmM6XY0Z0snY1b2w_34zzMDcFArq8r1XxXuMvQOxBQH6036bcY152Uoh9FZAHfWCbcAa2XSmVS_ZRkBnGgFWX7Fror0QwnSifc2uQLcWoNUb9vtupVgyLyOnp-wPSwz8ESmGhMR9HvgheZo8n3DqZ5-Rx8yXP8gPMxLmgBdhoTL5xKmktU9HoCwYM71hr0afCN-e9w37dff15-198_Dj2_fbLw9NUBKWRhoFdthZiVZZDQPAOHZ6FzwOaLS3IrS69RZ6bUeQ3lSkFwP0KGzQYNvdDft48q2H_65Ii5siBUypPl1WctpqaSzY_4JgpFJG7SqoTmCYC9GMozvMcfLzkwPhjhW4vTtV4I4VOAF1VJW9P_uv_YTDRXTOvAIfzoCn4NNYYw2RLpzplNIgK_f5xGGN7THi7CjEY-ZDnDEsbijx3588A-3Ap0k</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Trikash, I.O.</creator><creator>Kolchinskaya, L.I.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20060801</creationdate><title>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</title><author>Trikash, I.O. ; Kolchinskaya, L.I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Membrane - metabolism</topic><topic>Cell-free model system</topic><topic>Exocytosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Membrane fusion</topic><topic>Membrane Fusion - physiology</topic><topic>Membrane Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>SNARE proteins</topic><topic>SNARE Proteins - metabolism</topic><topic>Solubility</topic><topic>Synaptic Membranes - metabolism</topic><topic>Synaptic Vesicles - metabolism</topic><topic>Synaptosomes - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trikash, I.O.</creatorcontrib><creatorcontrib>Kolchinskaya, L.I.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurochemistry international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trikash, I.O.</au><au>Kolchinskaya, L.I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</atitle><jtitle>Neurochemistry international</jtitle><addtitle>Neurochem Int</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>49</volume><issue>3</issue><spage>270</spage><epage>275</epage><pages>270-275</pages><issn>0197-0186</issn><eissn>1872-9754</eissn><coden>NEUIDS</coden><abstract>Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca 2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca 2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16581156</pmid><doi>10.1016/j.neuint.2006.01.014</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0197-0186
ispartof Neurochemistry international, 2006-08, Vol.49 (3), p.270-275
issn 0197-0186
1872-9754
language eng
recordid cdi_proquest_miscellaneous_68627818
source ScienceDirect Journals
subjects Animals
Biological and medical sciences
Cell Membrane - metabolism
Cell-free model system
Exocytosis
Fundamental and applied biological sciences. Psychology
Membrane fusion
Membrane Fusion - physiology
Membrane Proteins - metabolism
Rats
Rats, Wistar
SNARE proteins
SNARE Proteins - metabolism
Solubility
Synaptic Membranes - metabolism
Synaptic Vesicles - metabolism
Synaptosomes - metabolism
Vertebrates: nervous system and sense organs
title Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T12%3A24%3A28IST&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=Fusion%20of%20synaptic%20vesicles%20and%20plasma%20membrane%20in%20the%20presence%20of%20synaptosomal%20soluble%20proteins&rft.jtitle=Neurochemistry%20international&rft.au=Trikash,%20I.O.&rft.date=2006-08-01&rft.volume=49&rft.issue=3&rft.spage=270&rft.epage=275&rft.pages=270-275&rft.issn=0197-0186&rft.eissn=1872-9754&rft.coden=NEUIDS&rft_id=info:doi/10.1016/j.neuint.2006.01.014&rft_dat=%3Cproquest_cross%3E68627818%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=17244743&rft_id=info:pmid/16581156&rfr_iscdi=true