Spontaneous and electrically-evoked catecholamine secretion from long-term cultures of bovine adrenal chromaffin cells
Abstract Catecholamine release was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period of three months. Cells were plated over simple biocompatible cell platforms with electrical stimulation capability and at specified times transferred to an acrylic superfu...
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description | Abstract Catecholamine release was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period of three months. Cells were plated over simple biocompatible cell platforms with electrical stimulation capability and at specified times transferred to an acrylic superfusion chamber designed to allow controlled flow of superfusate over the culture. Catecholamine release was measured from the superfusates using fast cyclic voltammetry before, during and after electrical stimulation of the cells. Immunocytochemical staining of CC cultures revealed that they were composed of epinephrine (EP) and/or norepinephrine (NE) type cells. Both spontaneous and evoked-release of catecholamines from CCs were observed throughout the testing period. EP predominated during spontaneous release, whereas NE was more prevalent during electrically-evoked release. Electrical stimulation for 20 s, increased total catecholamine release by 60–130% (measured over a period of 500 s) compared to that observed for an equivalent 20 s period of spontaneous release. Stimulus intensity was correlated with the amount of evoked release, up to a plateau which was observed near the highest intensities. Shorter intervals between stimulation trials did not significantly affect the initial amount of release, and the amount of evoked release was relatively stable over time and did not decrease significantly with age of the culture. The present study demonstrates long-term survival of CC cultures in vitro and describes a technique useful for rapid assessment of cell functionality and release properties of cultured monoaminergic cell types that later can be transplanted for neurotransmitter replacement following injury or disease. |
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Cells were plated over simple biocompatible cell platforms with electrical stimulation capability and at specified times transferred to an acrylic superfusion chamber designed to allow controlled flow of superfusate over the culture. Catecholamine release was measured from the superfusates using fast cyclic voltammetry before, during and after electrical stimulation of the cells. Immunocytochemical staining of CC cultures revealed that they were composed of epinephrine (EP) and/or norepinephrine (NE) type cells. Both spontaneous and evoked-release of catecholamines from CCs were observed throughout the testing period. EP predominated during spontaneous release, whereas NE was more prevalent during electrically-evoked release. Electrical stimulation for 20 s, increased total catecholamine release by 60–130% (measured over a period of 500 s) compared to that observed for an equivalent 20 s period of spontaneous release. Stimulus intensity was correlated with the amount of evoked release, up to a plateau which was observed near the highest intensities. Shorter intervals between stimulation trials did not significantly affect the initial amount of release, and the amount of evoked release was relatively stable over time and did not decrease significantly with age of the culture. The present study demonstrates long-term survival of CC cultures in vitro and describes a technique useful for rapid assessment of cell functionality and release properties of cultured monoaminergic cell types that later can be transplanted for neurotransmitter replacement following injury or disease.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2013.07.027</identifier><identifier>PMID: 23891791</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adrenal Glands - cytology ; Adrenals. Interrenals ; Adrenomedullary hormones. Regulation ; Animals ; Biological and medical sciences ; Biophysical Phenomena - physiology ; Biophysics ; brain ; Catecholamines ; Catecholamines - metabolism ; Cattle ; Cells, Cultured ; Chromaffin cells ; Chromaffin Cells - metabolism ; Chromaffin Cells - ultrastructure ; Electric Stimulation - methods ; electrical treatment ; Electrochemistry ; Epinephrine ; Evoked Potentials - physiology ; Fundamental and applied biological sciences. Psychology ; Microscopy, Electron, Scanning ; Neurology ; Norepinephrine ; Phenylethanolamine N-Methyltransferase - metabolism ; rapid methods ; Rats ; secretion ; Time Factors ; Transplantation ; Tyrosine 3-Monooxygenase ; Vertebrates: endocrinology ; Voltammetry</subject><ispartof>Brain research, 2013-09, Vol.1529, p.209-222</ispartof><rights>Elsevier B.V.</rights><rights>2013 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c457t-88fce2cf5a5f18a52b6fffc843d873951203b01b311e59950f70247e65f73bdf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.brainres.2013.07.027$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27663471$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23891791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Noga, Brian R</creatorcontrib><creatorcontrib>Pinzon, Alberto</creatorcontrib><title>Spontaneous and electrically-evoked catecholamine secretion from long-term cultures of bovine adrenal chromaffin cells</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Abstract Catecholamine release was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period of three months. Cells were plated over simple biocompatible cell platforms with electrical stimulation capability and at specified times transferred to an acrylic superfusion chamber designed to allow controlled flow of superfusate over the culture. Catecholamine release was measured from the superfusates using fast cyclic voltammetry before, during and after electrical stimulation of the cells. Immunocytochemical staining of CC cultures revealed that they were composed of epinephrine (EP) and/or norepinephrine (NE) type cells. Both spontaneous and evoked-release of catecholamines from CCs were observed throughout the testing period. EP predominated during spontaneous release, whereas NE was more prevalent during electrically-evoked release. Electrical stimulation for 20 s, increased total catecholamine release by 60–130% (measured over a period of 500 s) compared to that observed for an equivalent 20 s period of spontaneous release. Stimulus intensity was correlated with the amount of evoked release, up to a plateau which was observed near the highest intensities. Shorter intervals between stimulation trials did not significantly affect the initial amount of release, and the amount of evoked release was relatively stable over time and did not decrease significantly with age of the culture. The present study demonstrates long-term survival of CC cultures in vitro and describes a technique useful for rapid assessment of cell functionality and release properties of cultured monoaminergic cell types that later can be transplanted for neurotransmitter replacement following injury or disease.</description><subject>Adrenal Glands - cytology</subject><subject>Adrenals. Interrenals</subject><subject>Adrenomedullary hormones. Regulation</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biophysical Phenomena - physiology</subject><subject>Biophysics</subject><subject>brain</subject><subject>Catecholamines</subject><subject>Catecholamines - metabolism</subject><subject>Cattle</subject><subject>Cells, Cultured</subject><subject>Chromaffin cells</subject><subject>Chromaffin Cells - metabolism</subject><subject>Chromaffin Cells - ultrastructure</subject><subject>Electric Stimulation - methods</subject><subject>electrical treatment</subject><subject>Electrochemistry</subject><subject>Epinephrine</subject><subject>Evoked Potentials - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Microscopy, Electron, Scanning</subject><subject>Neurology</subject><subject>Norepinephrine</subject><subject>Phenylethanolamine N-Methyltransferase - metabolism</subject><subject>rapid methods</subject><subject>Rats</subject><subject>secretion</subject><subject>Time Factors</subject><subject>Transplantation</subject><subject>Tyrosine 3-Monooxygenase</subject><subject>Vertebrates: endocrinology</subject><subject>Voltammetry</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUQCMEokPhF4o3SGwy-BHbyQaBKl5SJRZD15bjXLeeOvZgJyPN3-MoU5DYdGVZOvd5blVdEbwlmIgP-22ftAsJ8pZiwrZYbjGVz6oNaSWtBW3w82qDMRZ123XsonqV8758Gevwy-qCsrYjsiOb6rg7xDDpAHHOSIcBgQczJWe096cajvEBBmT0BOY-ej26ACiDSTC5GJBNcUQ-hrt6gjQiM_tpLh2haFEfjwurhwRBe2TuC6qtdQEZ8D6_rl5Y7TO8Ob-X1e3XL7-uv9c3P7_9uP58U5uGy6luW2uAGss1t6TVnPbCWmvahg2tZB0nFLMek54RArzrOLYS00aC4FayfrDssnq_5j2k-HuGPKnR5aWDdWJFhMANYbwRT6MNFZw0uGUFFStqUsw5gVWH5EadTopgtehRe_WoRy16FJaq6CmBV-cacz_C8Dfs0UcB3p0BnYsCm3QwLv_jpBCskQv3duWsjkrfpcLc7kolXhyXtXRtIT6tBJT1Hh0klY2DYGBwqRhWQ3RPd_vxvxTGu7CcxgOcIO_jnIrbshmVqcJqt5zbcm2E4ZK2kewPDpnRLA</recordid><startdate>20130905</startdate><enddate>20130905</enddate><creator>Noga, Brian R</creator><creator>Pinzon, Alberto</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><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><scope>7TK</scope></search><sort><creationdate>20130905</creationdate><title>Spontaneous and electrically-evoked catecholamine secretion from long-term cultures of bovine adrenal chromaffin cells</title><author>Noga, Brian R ; Pinzon, Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-88fce2cf5a5f18a52b6fffc843d873951203b01b311e59950f70247e65f73bdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adrenal Glands - cytology</topic><topic>Adrenals. Interrenals</topic><topic>Adrenomedullary hormones. Regulation</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biophysical Phenomena - physiology</topic><topic>Biophysics</topic><topic>brain</topic><topic>Catecholamines</topic><topic>Catecholamines - metabolism</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>Chromaffin cells</topic><topic>Chromaffin Cells - metabolism</topic><topic>Chromaffin Cells - ultrastructure</topic><topic>Electric Stimulation - methods</topic><topic>electrical treatment</topic><topic>Electrochemistry</topic><topic>Epinephrine</topic><topic>Evoked Potentials - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Microscopy, Electron, Scanning</topic><topic>Neurology</topic><topic>Norepinephrine</topic><topic>Phenylethanolamine N-Methyltransferase - metabolism</topic><topic>rapid methods</topic><topic>Rats</topic><topic>secretion</topic><topic>Time Factors</topic><topic>Transplantation</topic><topic>Tyrosine 3-Monooxygenase</topic><topic>Vertebrates: endocrinology</topic><topic>Voltammetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noga, Brian R</creatorcontrib><creatorcontrib>Pinzon, Alberto</creatorcontrib><collection>AGRIS</collection><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><collection>Neurosciences Abstracts</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Noga, Brian R</au><au>Pinzon, Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spontaneous and electrically-evoked catecholamine secretion from long-term cultures of bovine adrenal chromaffin cells</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2013-09-05</date><risdate>2013</risdate><volume>1529</volume><spage>209</spage><epage>222</epage><pages>209-222</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract Catecholamine release was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period of three months. Cells were plated over simple biocompatible cell platforms with electrical stimulation capability and at specified times transferred to an acrylic superfusion chamber designed to allow controlled flow of superfusate over the culture. Catecholamine release was measured from the superfusates using fast cyclic voltammetry before, during and after electrical stimulation of the cells. Immunocytochemical staining of CC cultures revealed that they were composed of epinephrine (EP) and/or norepinephrine (NE) type cells. Both spontaneous and evoked-release of catecholamines from CCs were observed throughout the testing period. EP predominated during spontaneous release, whereas NE was more prevalent during electrically-evoked release. Electrical stimulation for 20 s, increased total catecholamine release by 60–130% (measured over a period of 500 s) compared to that observed for an equivalent 20 s period of spontaneous release. Stimulus intensity was correlated with the amount of evoked release, up to a plateau which was observed near the highest intensities. Shorter intervals between stimulation trials did not significantly affect the initial amount of release, and the amount of evoked release was relatively stable over time and did not decrease significantly with age of the culture. The present study demonstrates long-term survival of CC cultures in vitro and describes a technique useful for rapid assessment of cell functionality and release properties of cultured monoaminergic cell types that later can be transplanted for neurotransmitter replacement following injury or disease.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23891791</pmid><doi>10.1016/j.brainres.2013.07.027</doi><tpages>14</tpages></addata></record> |
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subjects | Adrenal Glands - cytology Adrenals. Interrenals Adrenomedullary hormones. Regulation Animals Biological and medical sciences Biophysical Phenomena - physiology Biophysics brain Catecholamines Catecholamines - metabolism Cattle Cells, Cultured Chromaffin cells Chromaffin Cells - metabolism Chromaffin Cells - ultrastructure Electric Stimulation - methods electrical treatment Electrochemistry Epinephrine Evoked Potentials - physiology Fundamental and applied biological sciences. Psychology Microscopy, Electron, Scanning Neurology Norepinephrine Phenylethanolamine N-Methyltransferase - metabolism rapid methods Rats secretion Time Factors Transplantation Tyrosine 3-Monooxygenase Vertebrates: endocrinology Voltammetry |
title | Spontaneous and electrically-evoked catecholamine secretion from long-term cultures of bovine adrenal chromaffin cells |
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