Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York Submitted 23 February 2007 ; accepted in final form 8 June 2007 We examined the permeabilities of homotypic and heterotypic gap junction (GJ) channels formed of rodent connexins (Cx) 30.2, 40, 43, and 45, which are expr...
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creator | Rackauskas, Mindaugas Verselis, Vytas K Bukauskas, Feliksas F |
description | Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York
Submitted 23 February 2007
; accepted in final form 8 June 2007
We examined the permeabilities of homotypic and heterotypic gap junction (GJ) channels formed of rodent connexins (Cx) 30.2, 40, 43, and 45, which are expressed in the heart and other tissues, using fluorescent dyes differing in net charge and molecular mass. Combining fluorescent imaging and electrophysiological recordings in the same cell pairs, we evaluated the single-channel permeability ( P ). All homotypic channels were permeable to the anionic monovalent dye Alexa Fluor-350 (AF 350 ), but mCx30.2 channels exhibited a significantly lower P than the others. The anionic divalent dye Lucifer yellow (LY) remained permeant in Cx40, Cx43, and Cx45 channels, but transfer through mCx30.2 channels was not detected. Heterotypic channels generally exhibited P values that were intermediate to the corresponding homotypic channels. P values of mCx30.2/Cx40, mCx30.2/Cx43, or mCx30.2/Cx45 heterotypic channels for AF 350 were similar and approximately twofold higher than P values of mCx30.2 homotypic channels. Permeabilities for cationic dyes were assessed only qualitatively because of their binding to nucleic acids. All homotypic and heterotypic channel configurations were permeable to ethidium bromide and 4,6-diamidino-2-phenylindole. Permeability for propidium iodide was limited only for GJ channels that contain at least one mCx30.2 hemichannel. In summary, we have demonstrated that Cx40, Cx43, and Cx45 are permeant to all examined cationic and anionic dyes, whereas mCx30.2 demonstrates permeation restrictions for molecules with molecular mass over 400 Da. The ratio of single-channel conductance to permeability for AF 350 was 40- to 170-fold higher for mCx30.2 than for Cx40, Cx43, and Cx45, suggesting that mCx30.2 GJs are notably more adapted to perform electrical rather than metabolic cell-cell communication.
connexin; gap junctions; dye; Lucifer yellow; 4,6-diamidino-2-phenylindole
Address for reprint requests and other correspondence: F. Bukauskas, 1300 Morris Park Ave., Albert Einstein College of Medicine, Bronx, NY 10461 (e-mail: fbukausk{at}aecom.yu.edu ) |
doi_str_mv | 10.1152/ajpheart.00234.2007 |
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Submitted 23 February 2007
; accepted in final form 8 June 2007
We examined the permeabilities of homotypic and heterotypic gap junction (GJ) channels formed of rodent connexins (Cx) 30.2, 40, 43, and 45, which are expressed in the heart and other tissues, using fluorescent dyes differing in net charge and molecular mass. Combining fluorescent imaging and electrophysiological recordings in the same cell pairs, we evaluated the single-channel permeability ( P ). All homotypic channels were permeable to the anionic monovalent dye Alexa Fluor-350 (AF 350 ), but mCx30.2 channels exhibited a significantly lower P than the others. The anionic divalent dye Lucifer yellow (LY) remained permeant in Cx40, Cx43, and Cx45 channels, but transfer through mCx30.2 channels was not detected. Heterotypic channels generally exhibited P values that were intermediate to the corresponding homotypic channels. P values of mCx30.2/Cx40, mCx30.2/Cx43, or mCx30.2/Cx45 heterotypic channels for AF 350 were similar and approximately twofold higher than P values of mCx30.2 homotypic channels. Permeabilities for cationic dyes were assessed only qualitatively because of their binding to nucleic acids. All homotypic and heterotypic channel configurations were permeable to ethidium bromide and 4,6-diamidino-2-phenylindole. Permeability for propidium iodide was limited only for GJ channels that contain at least one mCx30.2 hemichannel. In summary, we have demonstrated that Cx40, Cx43, and Cx45 are permeant to all examined cationic and anionic dyes, whereas mCx30.2 demonstrates permeation restrictions for molecules with molecular mass over 400 Da. The ratio of single-channel conductance to permeability for AF 350 was 40- to 170-fold higher for mCx30.2 than for Cx40, Cx43, and Cx45, suggesting that mCx30.2 GJs are notably more adapted to perform electrical rather than metabolic cell-cell communication.
connexin; gap junctions; dye; Lucifer yellow; 4,6-diamidino-2-phenylindole
Address for reprint requests and other correspondence: F. Bukauskas, 1300 Morris Park Ave., Albert Einstein College of Medicine, Bronx, NY 10461 (e-mail: fbukausk{at}aecom.yu.edu )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00234.2007</identifier><identifier>PMID: 17557922</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Cardiovascular system ; Cell Communication - physiology ; Cell Membrane Permeability - physiology ; Cells ; Connexins - physiology ; Ethidium - metabolism ; Fluorescent Dyes - metabolism ; Gap Junctions - physiology ; HeLa Cells ; Humans ; Indoles - metabolism ; Ions ; Isoquinolines - metabolism ; Membrane Potentials - physiology ; Molecular weight ; Permeability ; Proteins ; Rodentia ; Rodents</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2007-09, Vol.293 (3), p.H1729-H1736</ispartof><rights>Copyright American Physiological Society Sep 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-9b01ee32781dd101cadac0fba5decb8446b0e9991433e939f8bf8cf041f444f23</citedby><cites>FETCH-LOGICAL-c522t-9b01ee32781dd101cadac0fba5decb8446b0e9991433e939f8bf8cf041f444f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17557922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rackauskas, Mindaugas</creatorcontrib><creatorcontrib>Verselis, Vytas K</creatorcontrib><creatorcontrib>Bukauskas, Feliksas F</creatorcontrib><title>Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York
Submitted 23 February 2007
; accepted in final form 8 June 2007
We examined the permeabilities of homotypic and heterotypic gap junction (GJ) channels formed of rodent connexins (Cx) 30.2, 40, 43, and 45, which are expressed in the heart and other tissues, using fluorescent dyes differing in net charge and molecular mass. Combining fluorescent imaging and electrophysiological recordings in the same cell pairs, we evaluated the single-channel permeability ( P ). All homotypic channels were permeable to the anionic monovalent dye Alexa Fluor-350 (AF 350 ), but mCx30.2 channels exhibited a significantly lower P than the others. The anionic divalent dye Lucifer yellow (LY) remained permeant in Cx40, Cx43, and Cx45 channels, but transfer through mCx30.2 channels was not detected. Heterotypic channels generally exhibited P values that were intermediate to the corresponding homotypic channels. P values of mCx30.2/Cx40, mCx30.2/Cx43, or mCx30.2/Cx45 heterotypic channels for AF 350 were similar and approximately twofold higher than P values of mCx30.2 homotypic channels. Permeabilities for cationic dyes were assessed only qualitatively because of their binding to nucleic acids. All homotypic and heterotypic channel configurations were permeable to ethidium bromide and 4,6-diamidino-2-phenylindole. Permeability for propidium iodide was limited only for GJ channels that contain at least one mCx30.2 hemichannel. In summary, we have demonstrated that Cx40, Cx43, and Cx45 are permeant to all examined cationic and anionic dyes, whereas mCx30.2 demonstrates permeation restrictions for molecules with molecular mass over 400 Da. The ratio of single-channel conductance to permeability for AF 350 was 40- to 170-fold higher for mCx30.2 than for Cx40, Cx43, and Cx45, suggesting that mCx30.2 GJs are notably more adapted to perform electrical rather than metabolic cell-cell communication.
connexin; gap junctions; dye; Lucifer yellow; 4,6-diamidino-2-phenylindole
Address for reprint requests and other correspondence: F. Bukauskas, 1300 Morris Park Ave., Albert Einstein College of Medicine, Bronx, NY 10461 (e-mail: fbukausk{at}aecom.yu.edu )</description><subject>Animals</subject><subject>Cardiovascular system</subject><subject>Cell Communication - physiology</subject><subject>Cell Membrane Permeability - physiology</subject><subject>Cells</subject><subject>Connexins - physiology</subject><subject>Ethidium - metabolism</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Gap Junctions - physiology</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Indoles - metabolism</subject><subject>Ions</subject><subject>Isoquinolines - metabolism</subject><subject>Membrane Potentials - physiology</subject><subject>Molecular weight</subject><subject>Permeability</subject><subject>Proteins</subject><subject>Rodentia</subject><subject>Rodents</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kV2L1DAYhYMo7rj6CwQJXni1M5vPtkFYkMF1hQW9WK9DmibTDG1Sk1an_97Mh-MqeJMP3vMc3sMB4DVGK4w5uVbboTUqjiuECGUrglD5BCzyhCwxp-IpWCBa0GWBKb8AL1LaIoR4WdDn4AKXnJeCkAWYv5rYG1W7zo0zDBa2oQ_jPDgNlW9ga0YTT_-NGuB28np0wUPdKu9Nl6ANmW_2pFaxcUpDHfJk53yC_XpH0YpcwfWOocNJrw62-cVfgmdWdcm8Ot2X4Nvtx4f13fL-y6fP6w_3S52TjEtRI2wMJWWFmwYjrFWjNLK14o3RdcVYUSMjhMCMUiOosFVtK20Rw5YxZgm9BDdH32Gq86ba-DGqTg7R9SrOMign_55418pN-CFJRYtSFNng3ckghu-TSaPsXdKm65Q3YUqyqAhDFd8L3_4j3IYp-hxOEiJ4WQleZRE9inQMKUVjz5tgJPe9yt-9ykOvct9rpt48DvGHORWZBe-PgtZt2p8uGjm0c3KhC5tZ3k5d92B249maCCqpvMMlEXJobKav_0-f93lE0V_aw8e4</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Rackauskas, Mindaugas</creator><creator>Verselis, Vytas K</creator><creator>Bukauskas, Feliksas F</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20070901</creationdate><title>Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45</title><author>Rackauskas, Mindaugas ; Verselis, Vytas K ; Bukauskas, Feliksas F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-9b01ee32781dd101cadac0fba5decb8446b0e9991433e939f8bf8cf041f444f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Cardiovascular system</topic><topic>Cell Communication - physiology</topic><topic>Cell Membrane Permeability - physiology</topic><topic>Cells</topic><topic>Connexins - physiology</topic><topic>Ethidium - metabolism</topic><topic>Fluorescent Dyes - metabolism</topic><topic>Gap Junctions - physiology</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Indoles - metabolism</topic><topic>Ions</topic><topic>Isoquinolines - metabolism</topic><topic>Membrane Potentials - physiology</topic><topic>Molecular weight</topic><topic>Permeability</topic><topic>Proteins</topic><topic>Rodentia</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rackauskas, Mindaugas</creatorcontrib><creatorcontrib>Verselis, Vytas K</creatorcontrib><creatorcontrib>Bukauskas, Feliksas F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rackauskas, Mindaugas</au><au>Verselis, Vytas K</au><au>Bukauskas, Feliksas F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>293</volume><issue>3</issue><spage>H1729</spage><epage>H1736</epage><pages>H1729-H1736</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York
Submitted 23 February 2007
; accepted in final form 8 June 2007
We examined the permeabilities of homotypic and heterotypic gap junction (GJ) channels formed of rodent connexins (Cx) 30.2, 40, 43, and 45, which are expressed in the heart and other tissues, using fluorescent dyes differing in net charge and molecular mass. Combining fluorescent imaging and electrophysiological recordings in the same cell pairs, we evaluated the single-channel permeability ( P ). All homotypic channels were permeable to the anionic monovalent dye Alexa Fluor-350 (AF 350 ), but mCx30.2 channels exhibited a significantly lower P than the others. The anionic divalent dye Lucifer yellow (LY) remained permeant in Cx40, Cx43, and Cx45 channels, but transfer through mCx30.2 channels was not detected. Heterotypic channels generally exhibited P values that were intermediate to the corresponding homotypic channels. P values of mCx30.2/Cx40, mCx30.2/Cx43, or mCx30.2/Cx45 heterotypic channels for AF 350 were similar and approximately twofold higher than P values of mCx30.2 homotypic channels. Permeabilities for cationic dyes were assessed only qualitatively because of their binding to nucleic acids. All homotypic and heterotypic channel configurations were permeable to ethidium bromide and 4,6-diamidino-2-phenylindole. Permeability for propidium iodide was limited only for GJ channels that contain at least one mCx30.2 hemichannel. In summary, we have demonstrated that Cx40, Cx43, and Cx45 are permeant to all examined cationic and anionic dyes, whereas mCx30.2 demonstrates permeation restrictions for molecules with molecular mass over 400 Da. The ratio of single-channel conductance to permeability for AF 350 was 40- to 170-fold higher for mCx30.2 than for Cx40, Cx43, and Cx45, suggesting that mCx30.2 GJs are notably more adapted to perform electrical rather than metabolic cell-cell communication.
connexin; gap junctions; dye; Lucifer yellow; 4,6-diamidino-2-phenylindole
Address for reprint requests and other correspondence: F. Bukauskas, 1300 Morris Park Ave., Albert Einstein College of Medicine, Bronx, NY 10461 (e-mail: fbukausk{at}aecom.yu.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17557922</pmid><doi>10.1152/ajpheart.00234.2007</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cardiovascular system Cell Communication - physiology Cell Membrane Permeability - physiology Cells Connexins - physiology Ethidium - metabolism Fluorescent Dyes - metabolism Gap Junctions - physiology HeLa Cells Humans Indoles - metabolism Ions Isoquinolines - metabolism Membrane Potentials - physiology Molecular weight Permeability Proteins Rodentia Rodents |
title | Permeability of homotypic and heterotypic gap junction channels formed of cardiac connexins mCx30.2, Cx40, Cx43, and Cx45 |
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