Surface membrane remodeling following removal of vasopressin in toad urinary bladder
Vasopressin (ADH) increases transepithelial water flow in renal epithelia by a process that involves the insertion of water channels into the apical membrane. The objective of the present study was to examine membrane surface remodeling under conditions that promote the recovery of water channels. H...
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Veröffentlicht in: | Tissue & cell 1994-04, Vol.26 (2), p.189-201 |
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description | Vasopressin (ADH) increases transepithelial water flow in renal epithelia by a process that involves the insertion of water channels into the apical membrane. The objective of the present study was to examine membrane surface remodeling under conditions that promote the recovery of water channels. Hemibladders were set up as sacs with an imposed osmotic gradient. The control sacs received no hormone treatment, whereas the other sacs were stimulated with l00mU/ml ADH for 10 or 15 min to induce exocytosis and enhanced water flow. ADH was then washed from the tissues with fresh buffer rinses to abolish the hormone actions. These tissues were then allowed to recover for 15, 30 and 60 min. During this time water channels are recovered intracellularly by a process of endocytosis. This time period was called the retrieval period. At specified time intervals, tissues were fixed and processed for SEM or embedded in epon for ultrathin sectioning for TEM studies. Control tissues, regardless of the length of time, showed little or no sign of surface remodeling that was indicative of endocytosis during pre- or post-buffer washes, whereas the ADH- treated tissues showed a time-dependent remodeling of the apical membrane during activation and following removal of the hormone during the retrieval period. At the 10 min retrieval period, greater than 47% of the granular cells showed extensive surface remodeling. By 30 and 60 min post-hormone treatment during recovery, fewer than 23% of granular cells showed signs of surface membrane changes. During retrieval the apical membrane undergoes a transition with a loss of both microridges and microvilli prior to membrane restoration. These observations suggest that apical membrane remodeling is crucial for the restoration of membrane permeability following hormone activation and termination. |
doi_str_mv | 10.1016/0040-8166(94)90094-9 |
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The objective of the present study was to examine membrane surface remodeling under conditions that promote the recovery of water channels. Hemibladders were set up as sacs with an imposed osmotic gradient. The control sacs received no hormone treatment, whereas the other sacs were stimulated with l00mU/ml ADH for 10 or 15 min to induce exocytosis and enhanced water flow. ADH was then washed from the tissues with fresh buffer rinses to abolish the hormone actions. These tissues were then allowed to recover for 15, 30 and 60 min. During this time water channels are recovered intracellularly by a process of endocytosis. This time period was called the retrieval period. At specified time intervals, tissues were fixed and processed for SEM or embedded in epon for ultrathin sectioning for TEM studies. Control tissues, regardless of the length of time, showed little or no sign of surface remodeling that was indicative of endocytosis during pre- or post-buffer washes, whereas the ADH- treated tissues showed a time-dependent remodeling of the apical membrane during activation and following removal of the hormone during the retrieval period. At the 10 min retrieval period, greater than 47% of the granular cells showed extensive surface remodeling. By 30 and 60 min post-hormone treatment during recovery, fewer than 23% of granular cells showed signs of surface membrane changes. During retrieval the apical membrane undergoes a transition with a loss of both microridges and microvilli prior to membrane restoration. These observations suggest that apical membrane remodeling is crucial for the restoration of membrane permeability following hormone activation and termination.</description><identifier>ISSN: 0040-8166</identifier><identifier>EISSN: 1532-3072</identifier><identifier>DOI: 10.1016/0040-8166(94)90094-9</identifier><identifier>PMID: 8023324</identifier><identifier>CODEN: TICEBI</identifier><language>eng</language><publisher>Sidcup: Elsevier Ltd</publisher><subject>Animals ; Arginine Vasopressin - pharmacology ; Biological and medical sciences ; Biological Transport - drug effects ; Biological Transport - physiology ; Body Water - metabolism ; Bufo marinus ; Cell Membrane - drug effects ; Cell Membrane - physiology ; Endocytosis ; Fundamental and applied biological sciences. Psychology ; membrane recycling ; Microscopy, Electron ; Microscopy, Electron, Scanning ; Models, Biological ; renal epithelia ; Urinary Bladder - drug effects ; Urinary Bladder - physiology ; Urinary Bladder - ultrastructure ; vasopressin (ADH) ; Vasopressins - physiology ; Vertebrates: urinary system ; water flow</subject><ispartof>Tissue & cell, 1994-04, Vol.26 (2), p.189-201</ispartof><rights>1994</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-814bfb8096fcac473983a5ebf448790d5aa7a3cee6927feb8bdd50011652bf3f3</citedby><cites>FETCH-LOGICAL-c386t-814bfb8096fcac473983a5ebf448790d5aa7a3cee6927feb8bdd50011652bf3f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0040-8166(94)90094-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4183251$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8023324$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mia, A.J.</creatorcontrib><creatorcontrib>Oakford, L.X.</creatorcontrib><creatorcontrib>Yorio, T.</creatorcontrib><title>Surface membrane remodeling following removal of vasopressin in toad urinary bladder</title><title>Tissue & cell</title><addtitle>Tissue Cell</addtitle><description>Vasopressin (ADH) increases transepithelial water flow in renal epithelia by a process that involves the insertion of water channels into the apical membrane. The objective of the present study was to examine membrane surface remodeling under conditions that promote the recovery of water channels. Hemibladders were set up as sacs with an imposed osmotic gradient. The control sacs received no hormone treatment, whereas the other sacs were stimulated with l00mU/ml ADH for 10 or 15 min to induce exocytosis and enhanced water flow. ADH was then washed from the tissues with fresh buffer rinses to abolish the hormone actions. These tissues were then allowed to recover for 15, 30 and 60 min. During this time water channels are recovered intracellularly by a process of endocytosis. This time period was called the retrieval period. At specified time intervals, tissues were fixed and processed for SEM or embedded in epon for ultrathin sectioning for TEM studies. Control tissues, regardless of the length of time, showed little or no sign of surface remodeling that was indicative of endocytosis during pre- or post-buffer washes, whereas the ADH- treated tissues showed a time-dependent remodeling of the apical membrane during activation and following removal of the hormone during the retrieval period. At the 10 min retrieval period, greater than 47% of the granular cells showed extensive surface remodeling. By 30 and 60 min post-hormone treatment during recovery, fewer than 23% of granular cells showed signs of surface membrane changes. During retrieval the apical membrane undergoes a transition with a loss of both microridges and microvilli prior to membrane restoration. These observations suggest that apical membrane remodeling is crucial for the restoration of membrane permeability following hormone activation and termination.</description><subject>Animals</subject><subject>Arginine Vasopressin - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Biological Transport - physiology</subject><subject>Body Water - metabolism</subject><subject>Bufo marinus</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - physiology</subject><subject>Endocytosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>membrane recycling</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Electron, Scanning</subject><subject>Models, Biological</subject><subject>renal epithelia</subject><subject>Urinary Bladder - drug effects</subject><subject>Urinary Bladder - physiology</subject><subject>Urinary Bladder - ultrastructure</subject><subject>vasopressin (ADH)</subject><subject>Vasopressins - physiology</subject><subject>Vertebrates: urinary system</subject><subject>water flow</subject><issn>0040-8166</issn><issn>1532-3072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoMo67j6DxT6IKKH1konnU4uC7L4BQseXM8hHxWJpDtjMj3ivzftDHMUAglVTxVvHkKeU3hLgYp3ABx6SYV4rfgbBaB4rx6QHR3Z0DOYhodkd0Eekye1_gSAidPpilxJGBgb-I7cf1tLMA67GWdbzIJdwTl7THH50YWcUv69vbbi0aQuh-5oat4XrDUuXTuHbHy3lriY8qezyXiP5Sl5FEyq-Ox8X5PvHz_c337u775--nL7_q53TIpDC8ZtsBKUCM44PjElmRnRBs7lpMCPxkyGOUShhimgldb7EYBSMQ42sMCuyavT3n3Jv1asBz3H6jCl9o-8Vj2JUUg-ygbyE-hKrrVg0PsS55ZYU9CbTL2Z0psprbj-J1OrNvbivH-1M_rL0Nle67889011JoXmz8V6wTiVbBhpw25OGDYXx4hFVxdxcehjQXfQPsf_5_gLVESRVw</recordid><startdate>19940401</startdate><enddate>19940401</enddate><creator>Mia, A.J.</creator><creator>Oakford, L.X.</creator><creator>Yorio, T.</creator><general>Elsevier Ltd</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>19940401</creationdate><title>Surface membrane remodeling following removal of vasopressin in toad urinary bladder</title><author>Mia, A.J. ; Oakford, L.X. ; Yorio, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-814bfb8096fcac473983a5ebf448790d5aa7a3cee6927feb8bdd50011652bf3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Arginine Vasopressin - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Biological Transport - physiology</topic><topic>Body Water - metabolism</topic><topic>Bufo marinus</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - physiology</topic><topic>Endocytosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>membrane recycling</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Electron, Scanning</topic><topic>Models, Biological</topic><topic>renal epithelia</topic><topic>Urinary Bladder - drug effects</topic><topic>Urinary Bladder - physiology</topic><topic>Urinary Bladder - ultrastructure</topic><topic>vasopressin (ADH)</topic><topic>Vasopressins - physiology</topic><topic>Vertebrates: urinary system</topic><topic>water flow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mia, A.J.</creatorcontrib><creatorcontrib>Oakford, L.X.</creatorcontrib><creatorcontrib>Yorio, T.</creatorcontrib><collection>Pascal-Francis</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>Tissue & cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mia, A.J.</au><au>Oakford, L.X.</au><au>Yorio, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface membrane remodeling following removal of vasopressin in toad urinary bladder</atitle><jtitle>Tissue & cell</jtitle><addtitle>Tissue Cell</addtitle><date>1994-04-01</date><risdate>1994</risdate><volume>26</volume><issue>2</issue><spage>189</spage><epage>201</epage><pages>189-201</pages><issn>0040-8166</issn><eissn>1532-3072</eissn><coden>TICEBI</coden><abstract>Vasopressin (ADH) increases transepithelial water flow in renal epithelia by a process that involves the insertion of water channels into the apical membrane. The objective of the present study was to examine membrane surface remodeling under conditions that promote the recovery of water channels. Hemibladders were set up as sacs with an imposed osmotic gradient. The control sacs received no hormone treatment, whereas the other sacs were stimulated with l00mU/ml ADH for 10 or 15 min to induce exocytosis and enhanced water flow. ADH was then washed from the tissues with fresh buffer rinses to abolish the hormone actions. These tissues were then allowed to recover for 15, 30 and 60 min. During this time water channels are recovered intracellularly by a process of endocytosis. This time period was called the retrieval period. At specified time intervals, tissues were fixed and processed for SEM or embedded in epon for ultrathin sectioning for TEM studies. Control tissues, regardless of the length of time, showed little or no sign of surface remodeling that was indicative of endocytosis during pre- or post-buffer washes, whereas the ADH- treated tissues showed a time-dependent remodeling of the apical membrane during activation and following removal of the hormone during the retrieval period. At the 10 min retrieval period, greater than 47% of the granular cells showed extensive surface remodeling. By 30 and 60 min post-hormone treatment during recovery, fewer than 23% of granular cells showed signs of surface membrane changes. During retrieval the apical membrane undergoes a transition with a loss of both microridges and microvilli prior to membrane restoration. These observations suggest that apical membrane remodeling is crucial for the restoration of membrane permeability following hormone activation and termination.</abstract><cop>Sidcup</cop><pub>Elsevier Ltd</pub><pmid>8023324</pmid><doi>10.1016/0040-8166(94)90094-9</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Arginine Vasopressin - pharmacology Biological and medical sciences Biological Transport - drug effects Biological Transport - physiology Body Water - metabolism Bufo marinus Cell Membrane - drug effects Cell Membrane - physiology Endocytosis Fundamental and applied biological sciences. Psychology membrane recycling Microscopy, Electron Microscopy, Electron, Scanning Models, Biological renal epithelia Urinary Bladder - drug effects Urinary Bladder - physiology Urinary Bladder - ultrastructure vasopressin (ADH) Vasopressins - physiology Vertebrates: urinary system water flow |
title | Surface membrane remodeling following removal of vasopressin in toad urinary bladder |
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