Clusters of Intramembranous Particles on Cultured Myotubes at Sites that are Highly Sensitive to Acetylcholine
Electrophysiological and autoradiographic studies have shown that the distribution of acetylcholine (AcCho) receptors on uninnervated cultured chicken muscle cells is not uniform. Regions of high receptor density (hot spots) 10-40 times more sensitive than surrounding areas are localized as discrete...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1978-06, Vol.75 (6), p.3004-3008 |
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description | Electrophysiological and autoradiographic studies have shown that the distribution of acetylcholine (AcCho) receptors on uninnervated cultured chicken muscle cells is not uniform. Regions of high receptor density (hot spots) 10-40 times more sensitive than surrounding areas are localized as discrete patches or clusters about 10 μ m in diameter on myotube muscle membranes. Hot spots were also found on fusion-arrested mononucleated myoblasts. We have developed a method for freeze-fracturing monolayer cultures that allows the unambiguous reidentification of membrane patches previously assayed for AcCho sensitivity. The freeze-fractured membranes at physiologically defined hot spots contain aggregates of many (10-20) small clusters of large (10-19 nm in diameter) intramembranous particles. Clusters are found on both fracture faces, but the particle density is much greater on the protoplasmic (P) face than on the extracellular (E) face (about 2000/μ m2vs. 700/μ m2). Some of the particles appear to be composed of five or six ``subunits'' arranged cylindrically around a central dark dot. Because the aggregates are present at sites of high AcCho sensitivity, it is likely that the intramembranous particles are in some way related to the AcCho receptor molecule. |
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Clusters are found on both fracture faces, but the particle density is much greater on the protoplasmic (P) face than on the extracellular (E) face (about 2000/μ m2vs. 700/μ m2). Some of the particles appear to be composed of five or six ``subunits'' arranged cylindrically around a central dark dot. Because the aggregates are present at sites of high AcCho sensitivity, it is likely that the intramembranous particles are in some way related to the AcCho receptor molecule.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.75.6.3004</identifier><identifier>PMID: 96446</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Acetylcholine - pharmacology ; Animals ; B lymphocytes ; Bungarotoxins - metabolism ; Cell aggregates ; Cell Fusion ; Cells, Cultured ; Chick Embryo ; Cultured cells ; Egtazic Acid - pharmacology ; Electric Conductivity ; Electrophysiology ; Face ; Freeze Fracturing ; Gap junctions ; Muscle cells ; Muscle fibers ; Muscles - metabolism ; Muscles - ultrastructure ; Myoblasts ; Receptors ; Receptors, Cholinergic - metabolism ; Synaptic Membranes - ultrastructure</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1978-06, Vol.75 (6), p.3004-3008</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-6de82260dc3356f32f0bc98476bdb77d79d115faf683027e348614ff33fc48d13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/75/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/68375$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/68375$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/96446$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yee, A. G.</creatorcontrib><creatorcontrib>Fischbach, G. D.</creatorcontrib><creatorcontrib>Karnovsky, M. J.</creatorcontrib><title>Clusters of Intramembranous Particles on Cultured Myotubes at Sites that are Highly Sensitive to Acetylcholine</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Electrophysiological and autoradiographic studies have shown that the distribution of acetylcholine (AcCho) receptors on uninnervated cultured chicken muscle cells is not uniform. Regions of high receptor density (hot spots) 10-40 times more sensitive than surrounding areas are localized as discrete patches or clusters about 10 μ m in diameter on myotube muscle membranes. Hot spots were also found on fusion-arrested mononucleated myoblasts. We have developed a method for freeze-fracturing monolayer cultures that allows the unambiguous reidentification of membrane patches previously assayed for AcCho sensitivity. The freeze-fractured membranes at physiologically defined hot spots contain aggregates of many (10-20) small clusters of large (10-19 nm in diameter) intramembranous particles. Clusters are found on both fracture faces, but the particle density is much greater on the protoplasmic (P) face than on the extracellular (E) face (about 2000/μ m2vs. 700/μ m2). Some of the particles appear to be composed of five or six ``subunits'' arranged cylindrically around a central dark dot. Because the aggregates are present at sites of high AcCho sensitivity, it is likely that the intramembranous particles are in some way related to the AcCho receptor molecule.</description><subject>Acetylcholine - pharmacology</subject><subject>Animals</subject><subject>B lymphocytes</subject><subject>Bungarotoxins - metabolism</subject><subject>Cell aggregates</subject><subject>Cell Fusion</subject><subject>Cells, Cultured</subject><subject>Chick Embryo</subject><subject>Cultured cells</subject><subject>Egtazic Acid - pharmacology</subject><subject>Electric Conductivity</subject><subject>Electrophysiology</subject><subject>Face</subject><subject>Freeze Fracturing</subject><subject>Gap junctions</subject><subject>Muscle cells</subject><subject>Muscle fibers</subject><subject>Muscles - metabolism</subject><subject>Muscles - ultrastructure</subject><subject>Myoblasts</subject><subject>Receptors</subject><subject>Receptors, Cholinergic - metabolism</subject><subject>Synaptic Membranes - ultrastructure</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhS1EBUvhygGE5FNvSe3YsZMDh2pFaaWiIhXOlpOMu66ceLGdiv33ddhlVS6cPPL33tgzD6H3lJSUSHa-nXQsZV2KkhHCX6AVJS0tBG_JS7QipJJFwyv-Gr2J8YEQ0tYNeYVOWsG5WKFp7eaYIETsDb6eUtAjjF3Qk58j_q5Dsr2DDCe8nl2aAwz4286nucuXOuE7m3KRNrnUAfCVvd-4Hb6DKdpkHwEnjy96SDvXb7yzE7xFJ0a7CO8O5yn6efnlx_qquLn9er2-uCl63rBUiAGaqhJk6BmrhWGVIV3fNlyKbuikHGQ7UFobbUTD8oDAeCMoN4YxkxsMlJ2iz_u-27kbYehhmcypbbCjDjvltVX_kslu1L1_VKytRCuy_-zgD_7XDDGp0cYenNMT5M0oyQmvRF1nYbkX9sHHGMAc36BELfGoJR4layXUEk82fHz-s6P8Tx6ZfjrQxfWXPXef_Y8rMzuX4HfKwg974UNMPhyVeV-yZk9Vf67n</recordid><startdate>19780601</startdate><enddate>19780601</enddate><creator>Yee, A. G.</creator><creator>Fischbach, G. D.</creator><creator>Karnovsky, M. J.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19780601</creationdate><title>Clusters of Intramembranous Particles on Cultured Myotubes at Sites that are Highly Sensitive to Acetylcholine</title><author>Yee, A. G. ; Fischbach, G. D. ; Karnovsky, M. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-6de82260dc3356f32f0bc98476bdb77d79d115faf683027e348614ff33fc48d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Animals</topic><topic>B lymphocytes</topic><topic>Bungarotoxins - metabolism</topic><topic>Cell aggregates</topic><topic>Cell Fusion</topic><topic>Cells, Cultured</topic><topic>Chick Embryo</topic><topic>Cultured cells</topic><topic>Egtazic Acid - pharmacology</topic><topic>Electric Conductivity</topic><topic>Electrophysiology</topic><topic>Face</topic><topic>Freeze Fracturing</topic><topic>Gap junctions</topic><topic>Muscle cells</topic><topic>Muscle fibers</topic><topic>Muscles - metabolism</topic><topic>Muscles - ultrastructure</topic><topic>Myoblasts</topic><topic>Receptors</topic><topic>Receptors, Cholinergic - metabolism</topic><topic>Synaptic Membranes - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yee, A. G.</creatorcontrib><creatorcontrib>Fischbach, G. D.</creatorcontrib><creatorcontrib>Karnovsky, M. J.</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yee, A. G.</au><au>Fischbach, G. D.</au><au>Karnovsky, M. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clusters of Intramembranous Particles on Cultured Myotubes at Sites that are Highly Sensitive to Acetylcholine</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1978-06-01</date><risdate>1978</risdate><volume>75</volume><issue>6</issue><spage>3004</spage><epage>3008</epage><pages>3004-3008</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Electrophysiological and autoradiographic studies have shown that the distribution of acetylcholine (AcCho) receptors on uninnervated cultured chicken muscle cells is not uniform. Regions of high receptor density (hot spots) 10-40 times more sensitive than surrounding areas are localized as discrete patches or clusters about 10 μ m in diameter on myotube muscle membranes. Hot spots were also found on fusion-arrested mononucleated myoblasts. We have developed a method for freeze-fracturing monolayer cultures that allows the unambiguous reidentification of membrane patches previously assayed for AcCho sensitivity. The freeze-fractured membranes at physiologically defined hot spots contain aggregates of many (10-20) small clusters of large (10-19 nm in diameter) intramembranous particles. Clusters are found on both fracture faces, but the particle density is much greater on the protoplasmic (P) face than on the extracellular (E) face (about 2000/μ m2vs. 700/μ m2). Some of the particles appear to be composed of five or six ``subunits'' arranged cylindrically around a central dark dot. Because the aggregates are present at sites of high AcCho sensitivity, it is likely that the intramembranous particles are in some way related to the AcCho receptor molecule.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>96446</pmid><doi>10.1073/pnas.75.6.3004</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine - pharmacology Animals B lymphocytes Bungarotoxins - metabolism Cell aggregates Cell Fusion Cells, Cultured Chick Embryo Cultured cells Egtazic Acid - pharmacology Electric Conductivity Electrophysiology Face Freeze Fracturing Gap junctions Muscle cells Muscle fibers Muscles - metabolism Muscles - ultrastructure Myoblasts Receptors Receptors, Cholinergic - metabolism Synaptic Membranes - ultrastructure |
title | Clusters of Intramembranous Particles on Cultured Myotubes at Sites that are Highly Sensitive to Acetylcholine |
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