Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37
1 Department of Physiology and Biophysics, State University of New York at Stony Brook, Stony Brook, New York 11974; and 2 Department of Pediatrics, Washington University, St. Louis, Missouri 63110 Homomeric gap junction channels are composed solely of one connexin type, whereas heterotypic forms...
Gespeichert in:
Veröffentlicht in: | American Journal of Physiology: Cell Physiology 1997-10, Vol.273 (4), p.C1386-C1396 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | C1396 |
---|---|
container_issue | 4 |
container_start_page | C1386 |
container_title | American Journal of Physiology: Cell Physiology |
container_volume | 273 |
creator | Brink, P. R Cronin, K Banach, K Peterson, E Westphale, E. M Seul, K. H Ramanan, S. V Beyer, E. C |
description | 1 Department of Physiology and
Biophysics, State University of New York at Stony Brook, Stony
Brook, New York 11974; and
2 Department of Pediatrics,
Washington University, St. Louis, Missouri 63110
Homomeric gap junction channels are composed solely of one
connexin type, whereas heterotypic forms contain two homomeric hemichannels but the six identical connexins of each are different from
each other. A heteromeric gap junction channel is one that contains
different connexins within either or both hemichannels. The existence
of heteromeric forms has been suggested, and many cell types are known
to coexpress connexins. To determine if coexpressed connexins would
form heteromers, we cotransfected rat connexin43 (rCx43) and human
connexin37 (hCx37) into a cell line normally devoid of any connexin
expression and used dual whole cell patch clamp to compare the observed
gap junction channel activity with that seen in cells transfected only
with rCx43 or hCx37. We also cocultured cells transfected with hCx37 or
rCx43, in which one population was tagged with a fluorescent marker to
monitor heterotypic channel activity. The cotransfected cells possessed
channel types unlike the homotypic forms of rCx43 or hCx37 or the
heterotypic forms. In addition, the noninstantaneous transjunctional
conductance-transjunctional voltage
( G j / V j )
relationship for cotransfected cell pairs showed a large range of
variability that was unlike that of the homotypic or heterotypic form.
The heterotypic cell pairs displayed asymmetric voltage dependence. The
results from the heteromeric cell pairs are inconsistent with summed
behavior of two independent homotypic populations or mixed populations
of homotypic and heterotypic channels types. The
G j / V j
data imply that the connexin-to-connexin interactions are significantly
altered in cotransfected cell pairs relative to the homotypic and
heterotypic forms. Heteromeric channels are a population of channels
whose characteristics could well impact differently from their
homotypic counterparts with regard to multicellular coordinated
responses.
homotypic channels; heteromeric channels; heterotypic channels; voltage gating |
doi_str_mv | 10.1152/ajpcell.1997.273.4.c1386 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_highwire_physiology_ajpcell_273_4_C1386</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79392718</sourcerecordid><originalsourceid>FETCH-LOGICAL-c427t-fde70348f2e9653fa0be4e79b956caa982c03fe9aea6a034c5ca77d0fbb152ac3</originalsourceid><addsrcrecordid>eNp1kMFq3DAURUVoSadpPyEguujOjmTJltVdGZI2EOgm3VbI8tPYgy25kt1k_r4yMwkhkJXgvXMvTwchTElOaVlc6f1kYBhyKqXIC8FynhvK6uoMbdK6yGhZsXdoQ1jFsopy9gF9jHFPCOFFJc_RuWSlEHW5QX-u__UtOAPY-oA7mCH4EUJv8E5PeL84M_feYdNp52CIKzVCi22icNAzNj7NH3vHGdauxd0yavc8ZOITem_1EOHz6b1Av2-u77c_s7tfP2633-8ywwsxZ7YFQRivbQGyKpnVpAEOQjayrIzWsi4MYRakBl3pBJrSaCFaYpsmfVcbdoG-Hnun4P8uEGc19nE1pB34JSohmSwErRP45RW490tw6TZV0IqXNecsQfURMsHHGMCqKfSjDgdFiVr9q5N_tfpXyb_iarv6T9HLU__SJFHPwZPwtP923Hf9rnvoA6ipO8TeD353UDfLMNzD4_xU_6JYTa1N4fzt8NNJL6_5D-2Cqjs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>216458443</pqid></control><display><type>article</type><title>Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37</title><source>MEDLINE</source><source>American Physiological Society</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Brink, P. R ; Cronin, K ; Banach, K ; Peterson, E ; Westphale, E. M ; Seul, K. H ; Ramanan, S. V ; Beyer, E. C</creator><creatorcontrib>Brink, P. R ; Cronin, K ; Banach, K ; Peterson, E ; Westphale, E. M ; Seul, K. H ; Ramanan, S. V ; Beyer, E. C</creatorcontrib><description>1 Department of Physiology and
Biophysics, State University of New York at Stony Brook, Stony
Brook, New York 11974; and
2 Department of Pediatrics,
Washington University, St. Louis, Missouri 63110
Homomeric gap junction channels are composed solely of one
connexin type, whereas heterotypic forms contain two homomeric hemichannels but the six identical connexins of each are different from
each other. A heteromeric gap junction channel is one that contains
different connexins within either or both hemichannels. The existence
of heteromeric forms has been suggested, and many cell types are known
to coexpress connexins. To determine if coexpressed connexins would
form heteromers, we cotransfected rat connexin43 (rCx43) and human
connexin37 (hCx37) into a cell line normally devoid of any connexin
expression and used dual whole cell patch clamp to compare the observed
gap junction channel activity with that seen in cells transfected only
with rCx43 or hCx37. We also cocultured cells transfected with hCx37 or
rCx43, in which one population was tagged with a fluorescent marker to
monitor heterotypic channel activity. The cotransfected cells possessed
channel types unlike the homotypic forms of rCx43 or hCx37 or the
heterotypic forms. In addition, the noninstantaneous transjunctional
conductance-transjunctional voltage
( G j / V j )
relationship for cotransfected cell pairs showed a large range of
variability that was unlike that of the homotypic or heterotypic form.
The heterotypic cell pairs displayed asymmetric voltage dependence. The
results from the heteromeric cell pairs are inconsistent with summed
behavior of two independent homotypic populations or mixed populations
of homotypic and heterotypic channels types. The
G j / V j
data imply that the connexin-to-connexin interactions are significantly
altered in cotransfected cell pairs relative to the homotypic and
heterotypic forms. Heteromeric channels are a population of channels
whose characteristics could well impact differently from their
homotypic counterparts with regard to multicellular coordinated
responses.
homotypic channels; heteromeric channels; heterotypic channels; voltage gating</description><identifier>ISSN: 0363-6143</identifier><identifier>ISSN: 0002-9513</identifier><identifier>EISSN: 1522-1563</identifier><identifier>EISSN: 2163-5773</identifier><identifier>DOI: 10.1152/ajpcell.1997.273.4.c1386</identifier><identifier>PMID: 9357785</identifier><identifier>CODEN: AJPHAP</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Connexin 43 - biosynthesis ; Connexin 43 - chemistry ; Connexin 43 - physiology ; Connexins - biosynthesis ; Connexins - chemistry ; Connexins - physiology ; Gap Junction alpha-4 Protein ; Gap Junctions - physiology ; Humans ; Ion Channels - physiology ; Macromolecular Substances ; Membrane Potentials ; Mice ; Neuroblastoma ; Patch-Clamp Techniques ; Protein Multimerization ; Rats ; Recombinant Proteins - chemistry ; Recombinant Proteins - metabolism ; Transfection ; Tumor Cells, Cultured</subject><ispartof>American Journal of Physiology: Cell Physiology, 1997-10, Vol.273 (4), p.C1386-C1396</ispartof><rights>Copyright American Physiological Society Oct 1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-fde70348f2e9653fa0be4e79b956caa982c03fe9aea6a034c5ca77d0fbb152ac3</citedby><cites>FETCH-LOGICAL-c427t-fde70348f2e9653fa0be4e79b956caa982c03fe9aea6a034c5ca77d0fbb152ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9357785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brink, P. R</creatorcontrib><creatorcontrib>Cronin, K</creatorcontrib><creatorcontrib>Banach, K</creatorcontrib><creatorcontrib>Peterson, E</creatorcontrib><creatorcontrib>Westphale, E. M</creatorcontrib><creatorcontrib>Seul, K. H</creatorcontrib><creatorcontrib>Ramanan, S. V</creatorcontrib><creatorcontrib>Beyer, E. C</creatorcontrib><title>Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol</addtitle><description>1 Department of Physiology and
Biophysics, State University of New York at Stony Brook, Stony
Brook, New York 11974; and
2 Department of Pediatrics,
Washington University, St. Louis, Missouri 63110
Homomeric gap junction channels are composed solely of one
connexin type, whereas heterotypic forms contain two homomeric hemichannels but the six identical connexins of each are different from
each other. A heteromeric gap junction channel is one that contains
different connexins within either or both hemichannels. The existence
of heteromeric forms has been suggested, and many cell types are known
to coexpress connexins. To determine if coexpressed connexins would
form heteromers, we cotransfected rat connexin43 (rCx43) and human
connexin37 (hCx37) into a cell line normally devoid of any connexin
expression and used dual whole cell patch clamp to compare the observed
gap junction channel activity with that seen in cells transfected only
with rCx43 or hCx37. We also cocultured cells transfected with hCx37 or
rCx43, in which one population was tagged with a fluorescent marker to
monitor heterotypic channel activity. The cotransfected cells possessed
channel types unlike the homotypic forms of rCx43 or hCx37 or the
heterotypic forms. In addition, the noninstantaneous transjunctional
conductance-transjunctional voltage
( G j / V j )
relationship for cotransfected cell pairs showed a large range of
variability that was unlike that of the homotypic or heterotypic form.
The heterotypic cell pairs displayed asymmetric voltage dependence. The
results from the heteromeric cell pairs are inconsistent with summed
behavior of two independent homotypic populations or mixed populations
of homotypic and heterotypic channels types. The
G j / V j
data imply that the connexin-to-connexin interactions are significantly
altered in cotransfected cell pairs relative to the homotypic and
heterotypic forms. Heteromeric channels are a population of channels
whose characteristics could well impact differently from their
homotypic counterparts with regard to multicellular coordinated
responses.
homotypic channels; heteromeric channels; heterotypic channels; voltage gating</description><subject>Animals</subject><subject>Connexin 43 - biosynthesis</subject><subject>Connexin 43 - chemistry</subject><subject>Connexin 43 - physiology</subject><subject>Connexins - biosynthesis</subject><subject>Connexins - chemistry</subject><subject>Connexins - physiology</subject><subject>Gap Junction alpha-4 Protein</subject><subject>Gap Junctions - physiology</subject><subject>Humans</subject><subject>Ion Channels - physiology</subject><subject>Macromolecular Substances</subject><subject>Membrane Potentials</subject><subject>Mice</subject><subject>Neuroblastoma</subject><subject>Patch-Clamp Techniques</subject><subject>Protein Multimerization</subject><subject>Rats</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - metabolism</subject><subject>Transfection</subject><subject>Tumor Cells, Cultured</subject><issn>0363-6143</issn><issn>0002-9513</issn><issn>1522-1563</issn><issn>2163-5773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFq3DAURUVoSadpPyEguujOjmTJltVdGZI2EOgm3VbI8tPYgy25kt1k_r4yMwkhkJXgvXMvTwchTElOaVlc6f1kYBhyKqXIC8FynhvK6uoMbdK6yGhZsXdoQ1jFsopy9gF9jHFPCOFFJc_RuWSlEHW5QX-u__UtOAPY-oA7mCH4EUJv8E5PeL84M_feYdNp52CIKzVCi22icNAzNj7NH3vHGdauxd0yavc8ZOITem_1EOHz6b1Av2-u77c_s7tfP2633-8ywwsxZ7YFQRivbQGyKpnVpAEOQjayrIzWsi4MYRakBl3pBJrSaCFaYpsmfVcbdoG-Hnun4P8uEGc19nE1pB34JSohmSwErRP45RW490tw6TZV0IqXNecsQfURMsHHGMCqKfSjDgdFiVr9q5N_tfpXyb_iarv6T9HLU__SJFHPwZPwtP923Hf9rnvoA6ipO8TeD353UDfLMNzD4_xU_6JYTa1N4fzt8NNJL6_5D-2Cqjs</recordid><startdate>19971001</startdate><enddate>19971001</enddate><creator>Brink, P. R</creator><creator>Cronin, K</creator><creator>Banach, K</creator><creator>Peterson, E</creator><creator>Westphale, E. M</creator><creator>Seul, K. H</creator><creator>Ramanan, S. V</creator><creator>Beyer, E. C</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>7X8</scope></search><sort><creationdate>19971001</creationdate><title>Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37</title><author>Brink, P. R ; Cronin, K ; Banach, K ; Peterson, E ; Westphale, E. M ; Seul, K. H ; Ramanan, S. V ; Beyer, E. C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-fde70348f2e9653fa0be4e79b956caa982c03fe9aea6a034c5ca77d0fbb152ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Connexin 43 - biosynthesis</topic><topic>Connexin 43 - chemistry</topic><topic>Connexin 43 - physiology</topic><topic>Connexins - biosynthesis</topic><topic>Connexins - chemistry</topic><topic>Connexins - physiology</topic><topic>Gap Junction alpha-4 Protein</topic><topic>Gap Junctions - physiology</topic><topic>Humans</topic><topic>Ion Channels - physiology</topic><topic>Macromolecular Substances</topic><topic>Membrane Potentials</topic><topic>Mice</topic><topic>Neuroblastoma</topic><topic>Patch-Clamp Techniques</topic><topic>Protein Multimerization</topic><topic>Rats</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - metabolism</topic><topic>Transfection</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brink, P. R</creatorcontrib><creatorcontrib>Cronin, K</creatorcontrib><creatorcontrib>Banach, K</creatorcontrib><creatorcontrib>Peterson, E</creatorcontrib><creatorcontrib>Westphale, E. M</creatorcontrib><creatorcontrib>Seul, K. H</creatorcontrib><creatorcontrib>Ramanan, S. V</creatorcontrib><creatorcontrib>Beyer, E. C</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><jtitle>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brink, P. R</au><au>Cronin, K</au><au>Banach, K</au><au>Peterson, E</au><au>Westphale, E. M</au><au>Seul, K. H</au><au>Ramanan, S. V</au><au>Beyer, E. C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>273</volume><issue>4</issue><spage>C1386</spage><epage>C1396</epage><pages>C1386-C1396</pages><issn>0363-6143</issn><issn>0002-9513</issn><eissn>1522-1563</eissn><eissn>2163-5773</eissn><coden>AJPHAP</coden><abstract>1 Department of Physiology and
Biophysics, State University of New York at Stony Brook, Stony
Brook, New York 11974; and
2 Department of Pediatrics,
Washington University, St. Louis, Missouri 63110
Homomeric gap junction channels are composed solely of one
connexin type, whereas heterotypic forms contain two homomeric hemichannels but the six identical connexins of each are different from
each other. A heteromeric gap junction channel is one that contains
different connexins within either or both hemichannels. The existence
of heteromeric forms has been suggested, and many cell types are known
to coexpress connexins. To determine if coexpressed connexins would
form heteromers, we cotransfected rat connexin43 (rCx43) and human
connexin37 (hCx37) into a cell line normally devoid of any connexin
expression and used dual whole cell patch clamp to compare the observed
gap junction channel activity with that seen in cells transfected only
with rCx43 or hCx37. We also cocultured cells transfected with hCx37 or
rCx43, in which one population was tagged with a fluorescent marker to
monitor heterotypic channel activity. The cotransfected cells possessed
channel types unlike the homotypic forms of rCx43 or hCx37 or the
heterotypic forms. In addition, the noninstantaneous transjunctional
conductance-transjunctional voltage
( G j / V j )
relationship for cotransfected cell pairs showed a large range of
variability that was unlike that of the homotypic or heterotypic form.
The heterotypic cell pairs displayed asymmetric voltage dependence. The
results from the heteromeric cell pairs are inconsistent with summed
behavior of two independent homotypic populations or mixed populations
of homotypic and heterotypic channels types. The
G j / V j
data imply that the connexin-to-connexin interactions are significantly
altered in cotransfected cell pairs relative to the homotypic and
heterotypic forms. Heteromeric channels are a population of channels
whose characteristics could well impact differently from their
homotypic counterparts with regard to multicellular coordinated
responses.
homotypic channels; heteromeric channels; heterotypic channels; voltage gating</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>9357785</pmid><doi>10.1152/ajpcell.1997.273.4.c1386</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0363-6143 |
ispartof | American Journal of Physiology: Cell Physiology, 1997-10, Vol.273 (4), p.C1386-C1396 |
issn | 0363-6143 0002-9513 1522-1563 2163-5773 |
language | eng |
recordid | cdi_highwire_physiology_ajpcell_273_4_C1386 |
source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Animals Connexin 43 - biosynthesis Connexin 43 - chemistry Connexin 43 - physiology Connexins - biosynthesis Connexins - chemistry Connexins - physiology Gap Junction alpha-4 Protein Gap Junctions - physiology Humans Ion Channels - physiology Macromolecular Substances Membrane Potentials Mice Neuroblastoma Patch-Clamp Techniques Protein Multimerization Rats Recombinant Proteins - chemistry Recombinant Proteins - metabolism Transfection Tumor Cells, Cultured |
title | Evidence for heteromeric gap junction channels formed from rat connexin43 and human connexin37 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T15%3A28%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evidence%20for%20heteromeric%20gap%20junction%20channels%20formed%20from%20rat%20connexin43%20and%20human%20connexin37&rft.jtitle=American%20Journal%20of%20Physiology:%20Cell%20Physiology&rft.au=Brink,%20P.%20R&rft.date=1997-10-01&rft.volume=273&rft.issue=4&rft.spage=C1386&rft.epage=C1396&rft.pages=C1386-C1396&rft.issn=0363-6143&rft.eissn=1522-1563&rft.coden=AJPHAP&rft_id=info:doi/10.1152/ajpcell.1997.273.4.c1386&rft_dat=%3Cproquest_pubme%3E79392718%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=216458443&rft_id=info:pmid/9357785&rfr_iscdi=true |