Electrophysiological Properties of Gap Junctions between Dissociated Pairs of Rat Hepatocytes
Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundan...
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Veröffentlicht in: | The Journal of cell biology 1986-07, Vol.103 (1), p.135-144 |
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description | Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundant gap and tight junctions. These cell pairs are strongly dye-coupled; Lucifer Yellow CH injected into one cell rapidly diffuses to the other. Pairs of hepatocytes are closely coupled electrically. Conductance of the junctional membrane is not voltage sensitive: voltage clamp studies demonstrate that g j is constant in response to long (5 s) transjunctional voltage steps of either polarity (to > ±40 mV from rest). Junctional conductance ( g j) between hepatocyte pairs is reduced by exposure to octanol (0.1 mM) and by intracellular acidification. Normal intracellular pH ( pH i), measured with a liquid ion exchange microelectrode, was generally 7.1-7.4, and superfusion with saline equilibrated with 100% CO2 reduced pH i to 6.0-6.5. In the pH i range 7.5-6.6, g j was constant. Below pH 6.6, g j steeply decreased and at 6.1 coupling was undetectable. pH i recovered when cells were rinsed with normal saline; in most cases g j recovered in parallel so that g j values were similar for pHs obtained during acidification or recovery. The low apparent pK and very steep pH i- g j relation of the liver gap junction contrast with higher pKs and more gradually rising curves in other tissues. If H+ ions act directly on the junctional molecules, the channels that are presumably homologous in different tissues must differ with respect to reactive sites or their environment. |
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C. ; Ginzberg, R. D. ; Morales, E. A. ; Gatmaitan, Z. ; Arias, I. M.</creator><creatorcontrib>Spray, D. C. ; Ginzberg, R. D. ; Morales, E. A. ; Gatmaitan, Z. ; Arias, I. M.</creatorcontrib><description>Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundant gap and tight junctions. These cell pairs are strongly dye-coupled; Lucifer Yellow CH injected into one cell rapidly diffuses to the other. Pairs of hepatocytes are closely coupled electrically. Conductance of the junctional membrane is not voltage sensitive: voltage clamp studies demonstrate that g j is constant in response to long (5 s) transjunctional voltage steps of either polarity (to > ±40 mV from rest). Junctional conductance ( g j) between hepatocyte pairs is reduced by exposure to octanol (0.1 mM) and by intracellular acidification. Normal intracellular pH ( pH i), measured with a liquid ion exchange microelectrode, was generally 7.1-7.4, and superfusion with saline equilibrated with 100% CO2 reduced pH i to 6.0-6.5. In the pH i range 7.5-6.6, g j was constant. Below pH 6.6, g j steeply decreased and at 6.1 coupling was undetectable. pH i recovered when cells were rinsed with normal saline; in most cases g j recovered in parallel so that g j values were similar for pHs obtained during acidification or recovery. The low apparent pK and very steep pH i- g j relation of the liver gap junction contrast with higher pKs and more gradually rising curves in other tissues. If H+ ions act directly on the junctional molecules, the channels that are presumably homologous in different tissues must differ with respect to reactive sites or their environment.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.103.1.135</identifier><identifier>PMID: 3722262</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>New York, NY: Rockefeller University Press</publisher><subject>Acidification ; Animals ; Biological and medical sciences ; Cell Adhesion ; Cell Communication - drug effects ; Cell membranes. Ionic channels. Membrane pores ; Cell structures and functions ; Cells ; Electric Conductivity ; Electric current ; Electric potential ; Electrodes ; Freeze Fracturing ; Fundamental and applied biological sciences. Psychology ; Gap junctions ; Hepatocytes ; Hydrogen-Ion Concentration ; Intercellular Junctions - physiology ; Liver ; Liver - cytology ; Liver - physiology ; Liver cells ; Membrane Potentials - drug effects ; Microscopy, Electron ; Molecular and cellular biology ; Octanols ; Octanols - pharmacology ; Rats</subject><ispartof>The Journal of cell biology, 1986-07, Vol.103 (1), p.135-144</ispartof><rights>Copyright 1986 The Rockefeller University Press</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-eeb062c57a7f44b6eee88d5c59eef1338b36356530386fa51775369a53b514703</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113793/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113793/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7948674$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3722262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spray, D. C.</creatorcontrib><creatorcontrib>Ginzberg, R. D.</creatorcontrib><creatorcontrib>Morales, E. A.</creatorcontrib><creatorcontrib>Gatmaitan, Z.</creatorcontrib><creatorcontrib>Arias, I. M.</creatorcontrib><title>Electrophysiological Properties of Gap Junctions between Dissociated Pairs of Rat Hepatocytes</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundant gap and tight junctions. These cell pairs are strongly dye-coupled; Lucifer Yellow CH injected into one cell rapidly diffuses to the other. Pairs of hepatocytes are closely coupled electrically. Conductance of the junctional membrane is not voltage sensitive: voltage clamp studies demonstrate that g j is constant in response to long (5 s) transjunctional voltage steps of either polarity (to > ±40 mV from rest). Junctional conductance ( g j) between hepatocyte pairs is reduced by exposure to octanol (0.1 mM) and by intracellular acidification. Normal intracellular pH ( pH i), measured with a liquid ion exchange microelectrode, was generally 7.1-7.4, and superfusion with saline equilibrated with 100% CO2 reduced pH i to 6.0-6.5. In the pH i range 7.5-6.6, g j was constant. Below pH 6.6, g j steeply decreased and at 6.1 coupling was undetectable. pH i recovered when cells were rinsed with normal saline; in most cases g j recovered in parallel so that g j values were similar for pHs obtained during acidification or recovery. The low apparent pK and very steep pH i- g j relation of the liver gap junction contrast with higher pKs and more gradually rising curves in other tissues. If H+ ions act directly on the junctional molecules, the channels that are presumably homologous in different tissues must differ with respect to reactive sites or their environment.</description><subject>Acidification</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Adhesion</subject><subject>Cell Communication - drug effects</subject><subject>Cell membranes. Ionic channels. Membrane pores</subject><subject>Cell structures and functions</subject><subject>Cells</subject><subject>Electric Conductivity</subject><subject>Electric current</subject><subject>Electric potential</subject><subject>Electrodes</subject><subject>Freeze Fracturing</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gap junctions</subject><subject>Hepatocytes</subject><subject>Hydrogen-Ion Concentration</subject><subject>Intercellular Junctions - physiology</subject><subject>Liver</subject><subject>Liver - cytology</subject><subject>Liver - physiology</subject><subject>Liver cells</subject><subject>Membrane Potentials - drug effects</subject><subject>Microscopy, Electron</subject><subject>Molecular and cellular biology</subject><subject>Octanols</subject><subject>Octanols - pharmacology</subject><subject>Rats</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEQhq0KVELaY2-ttAfEbYPt8cfuBQmV0oIqtUJwRJbXmW0dbdaL7YDy7zEkCvTEySPPo3dm9BByxuiC0QberFxXCliwBQN5RGZMClo3TNBnZEYpZ3UruXxBXqa0opQKLeCYHIPmnCs-I9-uBnQ5hulxm3wYwoN3dqjuywfG7DFVoa-u7VR92owu-zCmqsP8E3Gs3vuUgvM247K6tz7-QT_bXN3gZHNw24zphDzv7ZDwdP_OydcPV18ub-rbu-uPl-9uayd5m2vEjirupLa6F6JTiNg0S-lki9gzgKYDBVJJoNCo3kqmtQTVWgmdZEJTmJO3u9xp061x6XDM0Q5min5t49YE683TzugfzUP4YThjoFsoAa_3ATF832DKZu2Tw2GwI4ZNMlq1VDZl6v_Asg5jSvEC1jvQxZBSxP6wDaPmtzhTxJUCDDNFXOEv_j3hQO9Nlf6rfd-moqiPdnQ-HTDdikYVt3NyvsNWKYf4d6ZinIoWfgFKzqtj</recordid><startdate>19860701</startdate><enddate>19860701</enddate><creator>Spray, D. C.</creator><creator>Ginzberg, R. D.</creator><creator>Morales, E. A.</creator><creator>Gatmaitan, Z.</creator><creator>Arias, I. M.</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19860701</creationdate><title>Electrophysiological Properties of Gap Junctions between Dissociated Pairs of Rat Hepatocytes</title><author>Spray, D. C. ; Ginzberg, R. D. ; Morales, E. A. ; Gatmaitan, Z. ; Arias, I. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-eeb062c57a7f44b6eee88d5c59eef1338b36356530386fa51775369a53b514703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Acidification</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Adhesion</topic><topic>Cell Communication - drug effects</topic><topic>Cell membranes. Ionic channels. Membrane pores</topic><topic>Cell structures and functions</topic><topic>Cells</topic><topic>Electric Conductivity</topic><topic>Electric current</topic><topic>Electric potential</topic><topic>Electrodes</topic><topic>Freeze Fracturing</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gap junctions</topic><topic>Hepatocytes</topic><topic>Hydrogen-Ion Concentration</topic><topic>Intercellular Junctions - physiology</topic><topic>Liver</topic><topic>Liver - cytology</topic><topic>Liver - physiology</topic><topic>Liver cells</topic><topic>Membrane Potentials - drug effects</topic><topic>Microscopy, Electron</topic><topic>Molecular and cellular biology</topic><topic>Octanols</topic><topic>Octanols - pharmacology</topic><topic>Rats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spray, D. C.</creatorcontrib><creatorcontrib>Ginzberg, R. D.</creatorcontrib><creatorcontrib>Morales, E. A.</creatorcontrib><creatorcontrib>Gatmaitan, Z.</creatorcontrib><creatorcontrib>Arias, I. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrophysiological Properties of Gap Junctions between Dissociated Pairs of Rat Hepatocytes</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>1986-07-01</date><risdate>1986</risdate><volume>103</volume><issue>1</issue><spage>135</spage><epage>144</epage><pages>135-144</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundant gap and tight junctions. These cell pairs are strongly dye-coupled; Lucifer Yellow CH injected into one cell rapidly diffuses to the other. Pairs of hepatocytes are closely coupled electrically. Conductance of the junctional membrane is not voltage sensitive: voltage clamp studies demonstrate that g j is constant in response to long (5 s) transjunctional voltage steps of either polarity (to > ±40 mV from rest). Junctional conductance ( g j) between hepatocyte pairs is reduced by exposure to octanol (0.1 mM) and by intracellular acidification. Normal intracellular pH ( pH i), measured with a liquid ion exchange microelectrode, was generally 7.1-7.4, and superfusion with saline equilibrated with 100% CO2 reduced pH i to 6.0-6.5. In the pH i range 7.5-6.6, g j was constant. Below pH 6.6, g j steeply decreased and at 6.1 coupling was undetectable. pH i recovered when cells were rinsed with normal saline; in most cases g j recovered in parallel so that g j values were similar for pHs obtained during acidification or recovery. The low apparent pK and very steep pH i- g j relation of the liver gap junction contrast with higher pKs and more gradually rising curves in other tissues. If H+ ions act directly on the junctional molecules, the channels that are presumably homologous in different tissues must differ with respect to reactive sites or their environment.</abstract><cop>New York, NY</cop><pub>Rockefeller University Press</pub><pmid>3722262</pmid><doi>10.1083/jcb.103.1.135</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acidification Animals Biological and medical sciences Cell Adhesion Cell Communication - drug effects Cell membranes. Ionic channels. Membrane pores Cell structures and functions Cells Electric Conductivity Electric current Electric potential Electrodes Freeze Fracturing Fundamental and applied biological sciences. Psychology Gap junctions Hepatocytes Hydrogen-Ion Concentration Intercellular Junctions - physiology Liver Liver - cytology Liver - physiology Liver cells Membrane Potentials - drug effects Microscopy, Electron Molecular and cellular biology Octanols Octanols - pharmacology Rats |
title | Electrophysiological Properties of Gap Junctions between Dissociated Pairs of Rat Hepatocytes |
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