Loading…
Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures
The axolemma is associated structurally and functionally with the axoplasm, forming an axolemma-ectoplasm complex. To study the structure of this complex, a new technique was developed for removing the Schwann sheath from a portion of the giant nerve fiber. An isolated fiber was treated, without los...
Saved in:
Published in: | Cell and tissue research 1981-01, Vol.221 (1), p.1-15 |
---|---|
Main Authors: | , , , |
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-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3 |
container_end_page | 15 |
container_issue | 1 |
container_start_page | 1 |
container_title | Cell and tissue research |
container_volume | 221 |
creator | Metuzals, J Tasaki, I Terakawa, S Clapin, D.F |
description | The axolemma is associated structurally and functionally with the axoplasm, forming an axolemma-ectoplasm complex. To study the structure of this complex, a new technique was developed for removing the Schwann sheath from a portion of the giant nerve fiber. An isolated fiber was treated, without loss of excitability, with trypsin dissolved in natural seawater. Next, the fiber was treated with a mild fixative and then was placed in a hypertonic solution of sucrose in seawater. The elevated sheath was transected and everted, thus exposing the surface of the axon. Desheathed axons were examined by scanning and transmission electron microscopy. The surface of the axon has a ridge-and-groove pattern, reflecting an underlying helical arrangement of filaments which bundle and unbundle. Both left and right axons of the squid possess right-handed helical twists with a tilt angle of 10 degrees. Hemispherical protuberances about 1.5 microns at their base are observed along the ridges. Thin sections of the desheathed axons reveal that the desheathing procedure leaves the axolemma intact. Desheathed axons display electron-dense bodies associated with the axolemma and with the filaments of the ectoplasm similar to the dense bodies observed in whole fibers fixed in the presence of 10 mM Co(II) ions. Axons perfused for 40 min with a solution containing 2 mM Co(II) ions retain their excitability and display a smooth inner ectoplasmic face. A portion of the axolemma, together with adhering ectoplasm, was removed from desheathed axons, mounted between folding double grids, stained, and critical-point dried. Through this novel method a network of 10 nm filaments spaced 40 nm apart and cross-linked by filaments 5 to 7 nm in diameter was demonstrated. |
doi_str_mv | 10.1007/BF00216566 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73797719</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73797719</sourcerecordid><originalsourceid>FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3</originalsourceid><addsrcrecordid>eNpFkUtvFDEQhC0ECkvgwh3hEwekSfyY9YMbRAQiRYpEiMRt1ONpZ43G443tCeSn5N9mN7uBU0tVX5fUXYS85eyIM6aPv5wyJrhaKvWMLHgrRcOMNs_JgkkmGq3Ur5fkVSm_GeOtUvaAHGgmhWZiQe5_YEy3MNLkaV0hvXSrPzBNtKwQ6or6nOKjfh1gqnTCfIvUhx7z00K5mcPwicJEcURXc5qaGFxOxaV1cLTUebh7YuFvGjFG2NADhVKSC1Bx2OrrEUp85PPs6pyxvCYvPIwF3-znIbk6_frz5HtzfvHt7OTzeeMkU7XRYEwv0YAzQmrBbTsozaWyiMoMS2iN9dADtsKBtXxprexReoG9MNIoLw_Jh13uOqebGUvtYigOxxEmTHPptNRWa2434McduL2uZPTdOocI-a7jrNv20P3vYQO_26fOfcThH7p__MZ_v_M9pA6ucyjd1aVgXDJu9ZILIR8Aif2OYw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73797719</pqid></control><display><type>article</type><title>Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures</title><source>Springer LINK Archives</source><creator>Metuzals, J ; Tasaki, I ; Terakawa, S ; Clapin, D.F</creator><creatorcontrib>Metuzals, J ; Tasaki, I ; Terakawa, S ; Clapin, D.F</creatorcontrib><description>The axolemma is associated structurally and functionally with the axoplasm, forming an axolemma-ectoplasm complex. To study the structure of this complex, a new technique was developed for removing the Schwann sheath from a portion of the giant nerve fiber. An isolated fiber was treated, without loss of excitability, with trypsin dissolved in natural seawater. Next, the fiber was treated with a mild fixative and then was placed in a hypertonic solution of sucrose in seawater. The elevated sheath was transected and everted, thus exposing the surface of the axon. Desheathed axons were examined by scanning and transmission electron microscopy. The surface of the axon has a ridge-and-groove pattern, reflecting an underlying helical arrangement of filaments which bundle and unbundle. Both left and right axons of the squid possess right-handed helical twists with a tilt angle of 10 degrees. Hemispherical protuberances about 1.5 microns at their base are observed along the ridges. Thin sections of the desheathed axons reveal that the desheathing procedure leaves the axolemma intact. Desheathed axons display electron-dense bodies associated with the axolemma and with the filaments of the ectoplasm similar to the dense bodies observed in whole fibers fixed in the presence of 10 mM Co(II) ions. Axons perfused for 40 min with a solution containing 2 mM Co(II) ions retain their excitability and display a smooth inner ectoplasmic face. A portion of the axolemma, together with adhering ectoplasm, was removed from desheathed axons, mounted between folding double grids, stained, and critical-point dried. Through this novel method a network of 10 nm filaments spaced 40 nm apart and cross-linked by filaments 5 to 7 nm in diameter was demonstrated.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/BF00216566</identifier><identifier>PMID: 7032702</identifier><language>eng</language><publisher>Germany</publisher><subject>animal anatomy ; animal morphology ; animal physiology ; Animals ; aquatic organisms ; Axons - ultrastructure ; Cobalt ; Cytological Techniques ; Cytoplasm - ultrastructure ; Decapodiformes ; Fixatives ; Intracellular Membranes - ultrastructure ; Microscopy, Electron ; Microscopy, Electron, Scanning ; Myelin Sheath</subject><ispartof>Cell and tissue research, 1981-01, Vol.221 (1), p.1-15</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3</citedby><cites>FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7032702$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Metuzals, J</creatorcontrib><creatorcontrib>Tasaki, I</creatorcontrib><creatorcontrib>Terakawa, S</creatorcontrib><creatorcontrib>Clapin, D.F</creatorcontrib><title>Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>The axolemma is associated structurally and functionally with the axoplasm, forming an axolemma-ectoplasm complex. To study the structure of this complex, a new technique was developed for removing the Schwann sheath from a portion of the giant nerve fiber. An isolated fiber was treated, without loss of excitability, with trypsin dissolved in natural seawater. Next, the fiber was treated with a mild fixative and then was placed in a hypertonic solution of sucrose in seawater. The elevated sheath was transected and everted, thus exposing the surface of the axon. Desheathed axons were examined by scanning and transmission electron microscopy. The surface of the axon has a ridge-and-groove pattern, reflecting an underlying helical arrangement of filaments which bundle and unbundle. Both left and right axons of the squid possess right-handed helical twists with a tilt angle of 10 degrees. Hemispherical protuberances about 1.5 microns at their base are observed along the ridges. Thin sections of the desheathed axons reveal that the desheathing procedure leaves the axolemma intact. Desheathed axons display electron-dense bodies associated with the axolemma and with the filaments of the ectoplasm similar to the dense bodies observed in whole fibers fixed in the presence of 10 mM Co(II) ions. Axons perfused for 40 min with a solution containing 2 mM Co(II) ions retain their excitability and display a smooth inner ectoplasmic face. A portion of the axolemma, together with adhering ectoplasm, was removed from desheathed axons, mounted between folding double grids, stained, and critical-point dried. Through this novel method a network of 10 nm filaments spaced 40 nm apart and cross-linked by filaments 5 to 7 nm in diameter was demonstrated.</description><subject>animal anatomy</subject><subject>animal morphology</subject><subject>animal physiology</subject><subject>Animals</subject><subject>aquatic organisms</subject><subject>Axons - ultrastructure</subject><subject>Cobalt</subject><subject>Cytological Techniques</subject><subject>Cytoplasm - ultrastructure</subject><subject>Decapodiformes</subject><subject>Fixatives</subject><subject>Intracellular Membranes - ultrastructure</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Electron, Scanning</subject><subject>Myelin Sheath</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNpFkUtvFDEQhC0ECkvgwh3hEwekSfyY9YMbRAQiRYpEiMRt1ONpZ43G443tCeSn5N9mN7uBU0tVX5fUXYS85eyIM6aPv5wyJrhaKvWMLHgrRcOMNs_JgkkmGq3Ur5fkVSm_GeOtUvaAHGgmhWZiQe5_YEy3MNLkaV0hvXSrPzBNtKwQ6or6nOKjfh1gqnTCfIvUhx7z00K5mcPwicJEcURXc5qaGFxOxaV1cLTUebh7YuFvGjFG2NADhVKSC1Bx2OrrEUp85PPs6pyxvCYvPIwF3-znIbk6_frz5HtzfvHt7OTzeeMkU7XRYEwv0YAzQmrBbTsozaWyiMoMS2iN9dADtsKBtXxprexReoG9MNIoLw_Jh13uOqebGUvtYigOxxEmTHPptNRWa2434McduL2uZPTdOocI-a7jrNv20P3vYQO_26fOfcThH7p__MZ_v_M9pA6ucyjd1aVgXDJu9ZILIR8Aif2OYw</recordid><startdate>19810101</startdate><enddate>19810101</enddate><creator>Metuzals, J</creator><creator>Tasaki, I</creator><creator>Terakawa, S</creator><creator>Clapin, D.F</creator><scope>FBQ</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>7X8</scope></search><sort><creationdate>19810101</creationdate><title>Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures</title><author>Metuzals, J ; Tasaki, I ; Terakawa, S ; Clapin, D.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>animal anatomy</topic><topic>animal morphology</topic><topic>animal physiology</topic><topic>Animals</topic><topic>aquatic organisms</topic><topic>Axons - ultrastructure</topic><topic>Cobalt</topic><topic>Cytological Techniques</topic><topic>Cytoplasm - ultrastructure</topic><topic>Decapodiformes</topic><topic>Fixatives</topic><topic>Intracellular Membranes - ultrastructure</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Electron, Scanning</topic><topic>Myelin Sheath</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Metuzals, J</creatorcontrib><creatorcontrib>Tasaki, I</creatorcontrib><creatorcontrib>Terakawa, S</creatorcontrib><creatorcontrib>Clapin, D.F</creatorcontrib><collection>AGRIS</collection><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>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Metuzals, J</au><au>Tasaki, I</au><au>Terakawa, S</au><au>Clapin, D.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1981-01-01</date><risdate>1981</risdate><volume>221</volume><issue>1</issue><spage>1</spage><epage>15</epage><pages>1-15</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>The axolemma is associated structurally and functionally with the axoplasm, forming an axolemma-ectoplasm complex. To study the structure of this complex, a new technique was developed for removing the Schwann sheath from a portion of the giant nerve fiber. An isolated fiber was treated, without loss of excitability, with trypsin dissolved in natural seawater. Next, the fiber was treated with a mild fixative and then was placed in a hypertonic solution of sucrose in seawater. The elevated sheath was transected and everted, thus exposing the surface of the axon. Desheathed axons were examined by scanning and transmission electron microscopy. The surface of the axon has a ridge-and-groove pattern, reflecting an underlying helical arrangement of filaments which bundle and unbundle. Both left and right axons of the squid possess right-handed helical twists with a tilt angle of 10 degrees. Hemispherical protuberances about 1.5 microns at their base are observed along the ridges. Thin sections of the desheathed axons reveal that the desheathing procedure leaves the axolemma intact. Desheathed axons display electron-dense bodies associated with the axolemma and with the filaments of the ectoplasm similar to the dense bodies observed in whole fibers fixed in the presence of 10 mM Co(II) ions. Axons perfused for 40 min with a solution containing 2 mM Co(II) ions retain their excitability and display a smooth inner ectoplasmic face. A portion of the axolemma, together with adhering ectoplasm, was removed from desheathed axons, mounted between folding double grids, stained, and critical-point dried. Through this novel method a network of 10 nm filaments spaced 40 nm apart and cross-linked by filaments 5 to 7 nm in diameter was demonstrated.</abstract><cop>Germany</cop><pmid>7032702</pmid><doi>10.1007/BF00216566</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0302-766X |
ispartof | Cell and tissue research, 1981-01, Vol.221 (1), p.1-15 |
issn | 0302-766X 1432-0878 |
language | eng |
recordid | cdi_proquest_miscellaneous_73797719 |
source | Springer LINK Archives |
subjects | animal anatomy animal morphology animal physiology Animals aquatic organisms Axons - ultrastructure Cobalt Cytological Techniques Cytoplasm - ultrastructure Decapodiformes Fixatives Intracellular Membranes - ultrastructure Microscopy, Electron Microscopy, Electron, Scanning Myelin Sheath |
title | Removal of the Schwann sheath from the giant nerve fiber of the squid: an electron-microscopic study of the axolemma and associated axoplasmic structures |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T01%3A24%3A34IST&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=Removal%20of%20the%20Schwann%20sheath%20from%20the%20giant%20nerve%20fiber%20of%20the%20squid:%20an%20electron-microscopic%20study%20of%20the%20axolemma%20and%20associated%20axoplasmic%20structures&rft.jtitle=Cell%20and%20tissue%20research&rft.au=Metuzals,%20J&rft.date=1981-01-01&rft.volume=221&rft.issue=1&rft.spage=1&rft.epage=15&rft.pages=1-15&rft.issn=0302-766X&rft.eissn=1432-0878&rft_id=info:doi/10.1007/BF00216566&rft_dat=%3Cproquest_cross%3E73797719%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c306t-7a88b3e8ac82372194d671369ee68d5a489fabae42ca9915993be3f2eb28386f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=73797719&rft_id=info:pmid/7032702&rfr_iscdi=true |