Cellular differentiation in prostatic explant cultures: Assessed by electron microscopy and X-ray microanalysis
A method developed for X‐ray microanalysis (XRMA) of cell monolayers cultured on Formvar film has been shown to be well suited for the study of explant cultures of human prostate. Adherence and epithelial cell outgrowth occur as readily on the formvar as on ordinary tissue culture plastic, giving ri...
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Veröffentlicht in: | The Prostate 1992, Vol.21 (1), p.41-51 |
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description | A method developed for X‐ray microanalysis (XRMA) of cell monolayers cultured on Formvar film has been shown to be well suited for the study of explant cultures of human prostate. Adherence and epithelial cell outgrowth occur as readily on the formvar as on ordinary tissue culture plastic, giving rise to cultures with the same morphological characteristics. Conventional transmission electron microscopy revealed intracytoplasmic granules with the appearance of secretory vesicles. XRMA of electron‐dense intracytoplasmic granules in freeze‐dried cryosections showed significant local sequestration of calcium, but not of magnesium or zinc, elements that have previously been shown to colocalize with calcium in secretory granules in vivo. It is concluded that some aspects of the secretory phenotype are supported in this in vitro model. The factors regulating the expression of a differentiated phenotype in prostatic epithelium await further elucidation. XRMA may be useful in assessing the effects on secretory differentiation induced by variations in the Culture conditions. |
doi_str_mv | 10.1002/pros.2990210105 |
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Adherence and epithelial cell outgrowth occur as readily on the formvar as on ordinary tissue culture plastic, giving rise to cultures with the same morphological characteristics. Conventional transmission electron microscopy revealed intracytoplasmic granules with the appearance of secretory vesicles. XRMA of electron‐dense intracytoplasmic granules in freeze‐dried cryosections showed significant local sequestration of calcium, but not of magnesium or zinc, elements that have previously been shown to colocalize with calcium in secretory granules in vivo. It is concluded that some aspects of the secretory phenotype are supported in this in vitro model. The factors regulating the expression of a differentiated phenotype in prostatic epithelium await further elucidation. XRMA may be useful in assessing the effects on secretory differentiation induced by variations in the Culture conditions.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/pros.2990210105</identifier><identifier>PMID: 1379362</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Biopsy ; calcium ; Calcium - analysis ; Cell Differentiation - physiology ; Cell Membrane - ultrastructure ; Cell Nucleus - chemistry ; Cells, Cultured ; Cryoultramicrotomy - methods ; Culture Techniques ; Electron Probe Microanalysis - methods ; Epithelial Cells ; General aspects (metabolism, cell proliferation, established cell line...) ; human prostate ; Humans ; magnesium ; Magnesium - analysis ; Male ; Medical sciences ; Microscopy, Electron - methods ; Prostate - anatomy & histology ; Prostate - chemistry ; Prostate - cytology ; Prostatic Hyperplasia - pathology ; secretory granules ; Tumor cell ; Tumors ; zinc</subject><ispartof>The Prostate, 1992, Vol.21 (1), p.41-51</ispartof><rights>Copyright © 1992 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4115-20058dd8714ae54ec59f52e9b0dc6c7716fafd905ec6080ceafaedb0614826a83</citedby><cites>FETCH-LOGICAL-c4115-20058dd8714ae54ec59f52e9b0dc6c7716fafd905ec6080ceafaedb0614826a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpros.2990210105$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpros.2990210105$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5509166$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1379362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Halgunset, Jostein</creatorcontrib><creatorcontrib>Tvedt, KåRe E.</creatorcontrib><creatorcontrib>Kopstad, Gunnar</creatorcontrib><title>Cellular differentiation in prostatic explant cultures: Assessed by electron microscopy and X-ray microanalysis</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>A method developed for X‐ray microanalysis (XRMA) of cell monolayers cultured on Formvar film has been shown to be well suited for the study of explant cultures of human prostate. Adherence and epithelial cell outgrowth occur as readily on the formvar as on ordinary tissue culture plastic, giving rise to cultures with the same morphological characteristics. Conventional transmission electron microscopy revealed intracytoplasmic granules with the appearance of secretory vesicles. XRMA of electron‐dense intracytoplasmic granules in freeze‐dried cryosections showed significant local sequestration of calcium, but not of magnesium or zinc, elements that have previously been shown to colocalize with calcium in secretory granules in vivo. It is concluded that some aspects of the secretory phenotype are supported in this in vitro model. The factors regulating the expression of a differentiated phenotype in prostatic epithelium await further elucidation. XRMA may be useful in assessing the effects on secretory differentiation induced by variations in the Culture conditions.</description><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>calcium</subject><subject>Calcium - analysis</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Membrane - ultrastructure</subject><subject>Cell Nucleus - chemistry</subject><subject>Cells, Cultured</subject><subject>Cryoultramicrotomy - methods</subject><subject>Culture Techniques</subject><subject>Electron Probe Microanalysis - methods</subject><subject>Epithelial Cells</subject><subject>General aspects (metabolism, cell proliferation, established cell line...)</subject><subject>human prostate</subject><subject>Humans</subject><subject>magnesium</subject><subject>Magnesium - analysis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron - methods</subject><subject>Prostate - anatomy & histology</subject><subject>Prostate - chemistry</subject><subject>Prostate - cytology</subject><subject>Prostatic Hyperplasia - pathology</subject><subject>secretory granules</subject><subject>Tumor cell</subject><subject>Tumors</subject><subject>zinc</subject><issn>0270-4137</issn><issn>1097-0045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFv1DAQhS0EKkvhzAnJB8Qt7TiJ7QRO7QpapIoiCmpv1qw9kQzeZLET0fx7vMqqFSckS5Znvvc88xh7LeBEAJSnuzikk7JtoRQgQD5hKwGtLgBq-ZStoNRQ1KLSz9mLlH5CRrLoiB3lUlupcsWGNYUwBYzc-a6jSP3ocfRDz33P9-ZjfllO97uA_cjtFMYpUnrPz1KifBzfzJwC2TFmzdbbLLHDbubYO35XRJyXIvYY5uTTS_asw5Do1eE-Zj8-ffy-viyuri8-r8-uClsLIYsSQDbONVrUSLImK9tOltRuwFlltRaqw861IMkqaMASdkhuA0rUTamwqY7Zu8U37_B7ojSarU8274o9DVMyusppgdYZPF3A_eQpUmd20W8xzkaA2Uds9imYx4iz4s3BetpsyT3yS6a5__bQx2QxdBF769MDJiW0QqmMfViwPz7Q_L9fzddv1zf_DFEsap9Gun9QY_xllK60NLdfLsz5ua5u4PLW3FV_AYigp6U</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Halgunset, Jostein</creator><creator>Tvedt, KåRe E.</creator><creator>Kopstad, Gunnar</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</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></search><sort><creationdate>1992</creationdate><title>Cellular differentiation in prostatic explant cultures: Assessed by electron microscopy and X-ray microanalysis</title><author>Halgunset, Jostein ; Tvedt, KåRe E. ; Kopstad, Gunnar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4115-20058dd8714ae54ec59f52e9b0dc6c7716fafd905ec6080ceafaedb0614826a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>calcium</topic><topic>Calcium - analysis</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Membrane - ultrastructure</topic><topic>Cell Nucleus - chemistry</topic><topic>Cells, Cultured</topic><topic>Cryoultramicrotomy - methods</topic><topic>Culture Techniques</topic><topic>Electron Probe Microanalysis - methods</topic><topic>Epithelial Cells</topic><topic>General aspects (metabolism, cell proliferation, established cell line...)</topic><topic>human prostate</topic><topic>Humans</topic><topic>magnesium</topic><topic>Magnesium - analysis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron - methods</topic><topic>Prostate - anatomy & histology</topic><topic>Prostate - chemistry</topic><topic>Prostate - cytology</topic><topic>Prostatic Hyperplasia - pathology</topic><topic>secretory granules</topic><topic>Tumor cell</topic><topic>Tumors</topic><topic>zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halgunset, Jostein</creatorcontrib><creatorcontrib>Tvedt, KåRe E.</creatorcontrib><creatorcontrib>Kopstad, Gunnar</creatorcontrib><collection>Istex</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><jtitle>The Prostate</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halgunset, Jostein</au><au>Tvedt, KåRe E.</au><au>Kopstad, Gunnar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular differentiation in prostatic explant cultures: Assessed by electron microscopy and X-ray microanalysis</atitle><jtitle>The Prostate</jtitle><addtitle>Prostate</addtitle><date>1992</date><risdate>1992</risdate><volume>21</volume><issue>1</issue><spage>41</spage><epage>51</epage><pages>41-51</pages><issn>0270-4137</issn><eissn>1097-0045</eissn><coden>PRSTDS</coden><abstract>A method developed for X‐ray microanalysis (XRMA) of cell monolayers cultured on Formvar film has been shown to be well suited for the study of explant cultures of human prostate. Adherence and epithelial cell outgrowth occur as readily on the formvar as on ordinary tissue culture plastic, giving rise to cultures with the same morphological characteristics. Conventional transmission electron microscopy revealed intracytoplasmic granules with the appearance of secretory vesicles. XRMA of electron‐dense intracytoplasmic granules in freeze‐dried cryosections showed significant local sequestration of calcium, but not of magnesium or zinc, elements that have previously been shown to colocalize with calcium in secretory granules in vivo. It is concluded that some aspects of the secretory phenotype are supported in this in vitro model. The factors regulating the expression of a differentiated phenotype in prostatic epithelium await further elucidation. XRMA may be useful in assessing the effects on secretory differentiation induced by variations in the Culture conditions.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1379362</pmid><doi>10.1002/pros.2990210105</doi><tpages>11</tpages></addata></record> |
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subjects | Biological and medical sciences Biopsy calcium Calcium - analysis Cell Differentiation - physiology Cell Membrane - ultrastructure Cell Nucleus - chemistry Cells, Cultured Cryoultramicrotomy - methods Culture Techniques Electron Probe Microanalysis - methods Epithelial Cells General aspects (metabolism, cell proliferation, established cell line...) human prostate Humans magnesium Magnesium - analysis Male Medical sciences Microscopy, Electron - methods Prostate - anatomy & histology Prostate - chemistry Prostate - cytology Prostatic Hyperplasia - pathology secretory granules Tumor cell Tumors zinc |
title | Cellular differentiation in prostatic explant cultures: Assessed by electron microscopy and X-ray microanalysis |
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