Optimization of Non-isotopic in situ Hybridization: Detection of the Y Chromosome in Paraformaldehyde-Fixed, Wax-Embedded Cat Retina
A technique was developed to detect the Y chromosome in paraformaldehyde-fixed diethylglycoldiesterate-embedded cat retina. The Y chromosome specific DNA probe was labeled with digoxigenin through polymerase chain reaction incorporation. After treatment of paraformaldehyde-fixed, diethylglycoldieste...
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Veröffentlicht in: | Experimental eye research 1998-02, Vol.66 (2), p.223-230 |
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description | A technique was developed to detect the Y chromosome in paraformaldehyde-fixed diethylglycoldiesterate-embedded cat retina. The Y chromosome specific DNA probe was labeled with digoxigenin through polymerase chain reaction incorporation. After treatment of paraformaldehyde-fixed, diethylglycoldiesterate-embedded tissue sections with deoxyribonucleic acid decondensation and proteolytic digestion, non-fluorescent, non-isotopic in situ hybridization was performed on the retina sections. Most extensive treatment was required for the outer nuclear layer while the inner nuclear layer required more extensive treatment than the retinal pigment epithelial cells. Under optimal pretreatment conditions, the male cat retina displayed black spots which specifically localized at the periphery of the nuclei, while the female cat retina showed negative staining for the Y chromosome specific probe. The technique allows observation of the Y chromosome signal with preservation of retinal morphology and thus may be a valuable tool to discriminate donor cells in retinal pigment epithelial cell and photoreceptor cell transplants. |
doi_str_mv | 10.1006/exer.1997.0427 |
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The Y chromosome specific DNA probe was labeled with digoxigenin through polymerase chain reaction incorporation. After treatment of paraformaldehyde-fixed, diethylglycoldiesterate-embedded tissue sections with deoxyribonucleic acid decondensation and proteolytic digestion, non-fluorescent, non-isotopic in situ hybridization was performed on the retina sections. Most extensive treatment was required for the outer nuclear layer while the inner nuclear layer required more extensive treatment than the retinal pigment epithelial cells. Under optimal pretreatment conditions, the male cat retina displayed black spots which specifically localized at the periphery of the nuclei, while the female cat retina showed negative staining for the Y chromosome specific probe. The technique allows observation of the Y chromosome signal with preservation of retinal morphology and thus may be a valuable tool to discriminate donor cells in retinal pigment epithelial cell and photoreceptor cell transplants.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1006/exer.1997.0427</identifier><identifier>PMID: 9533848</identifier><identifier>CODEN: EXERA6</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; Cats ; Cell Nucleus - ultrastructure ; DNA - isolation & purification ; DNA Probes ; Eye and associated structures. Visual pathways and centers. Vision ; Formaldehyde ; Fundamental and applied biological sciences. Psychology ; in situ hybridization ; In Situ Hybridization - methods ; Male ; Paraffin Embedding - methods ; Photoreceptor Cells - ultrastructure ; photoreceptor transplantation ; Pigment Epithelium of Eye - ultrastructure ; Polymerase Chain Reaction ; Retina ; Retina - ultrastructure ; retinal pigment epithelial cell transplantation ; Staining and Labeling ; Vertebrates: nervous system and sense organs ; Y chromosome ; Y Chromosome - ultrastructure</subject><ispartof>Experimental eye research, 1998-02, Vol.66 (2), p.223-230</ispartof><rights>1998 Academic Press</rights><rights>1998 INIST-CNRS</rights><rights>Copyright 1998 Academic Press Limited.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-c21597fd5bca59343b569b69050a84408266b628529e6e35ec7605384e01acde3</citedby><cites>FETCH-LOGICAL-c368t-c21597fd5bca59343b569b69050a84408266b628529e6e35ec7605384e01acde3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014483597904279$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2204228$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9533848$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>YAO, RUIHONG</creatorcontrib><creatorcontrib>SUGINO, ILENE K.</creatorcontrib><creatorcontrib>GREULICH, KARIN M.</creatorcontrib><creatorcontrib>ISHIDA, MASAHIRO</creatorcontrib><creatorcontrib>WEIER, HEINZ-ULRICH G.</creatorcontrib><creatorcontrib>ZARBIN, MARCO A.</creatorcontrib><title>Optimization of Non-isotopic in situ Hybridization: Detection of the Y Chromosome in Paraformaldehyde-Fixed, Wax-Embedded Cat Retina</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>A technique was developed to detect the Y chromosome in paraformaldehyde-fixed diethylglycoldiesterate-embedded cat retina. The Y chromosome specific DNA probe was labeled with digoxigenin through polymerase chain reaction incorporation. After treatment of paraformaldehyde-fixed, diethylglycoldiesterate-embedded tissue sections with deoxyribonucleic acid decondensation and proteolytic digestion, non-fluorescent, non-isotopic in situ hybridization was performed on the retina sections. Most extensive treatment was required for the outer nuclear layer while the inner nuclear layer required more extensive treatment than the retinal pigment epithelial cells. Under optimal pretreatment conditions, the male cat retina displayed black spots which specifically localized at the periphery of the nuclei, while the female cat retina showed negative staining for the Y chromosome specific probe. The technique allows observation of the Y chromosome signal with preservation of retinal morphology and thus may be a valuable tool to discriminate donor cells in retinal pigment epithelial cell and photoreceptor cell transplants.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cats</subject><subject>Cell Nucleus - ultrastructure</subject><subject>DNA - isolation & purification</subject><subject>DNA Probes</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Formaldehyde</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>in situ hybridization</subject><subject>In Situ Hybridization - methods</subject><subject>Male</subject><subject>Paraffin Embedding - methods</subject><subject>Photoreceptor Cells - ultrastructure</subject><subject>photoreceptor transplantation</subject><subject>Pigment Epithelium of Eye - ultrastructure</subject><subject>Polymerase Chain Reaction</subject><subject>Retina</subject><subject>Retina - ultrastructure</subject><subject>retinal pigment epithelial cell transplantation</subject><subject>Staining and Labeling</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Y chromosome</subject><subject>Y Chromosome - ultrastructure</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM9rFDEYhoModVu9ehNyEE-dNZn8mIk3WVsrFCuiiKeQSb5hIzOTbZKVXc_-4WbYsTdPgXzP--bLg9ALStaUEPkGDhDXVKlmTXjdPEIrSpSsCCHNY7QihPKKt0w8Recp_Sy3jDf8DJ0pwVjL2xX6c7fLfvS_TfZhwqHHn8JU-RRy2HmL_YSTz3t8c-yidwv1Fr-HDPZfIG8B_8CbbQxjSGGEOfTZRNOHOJrBwfbooLr2B3CX-Ls5VFdjB86BwxuT8RfIfjLP0JPeDAmeL-cF-nZ99XVzU93effi4eXdbWSbbXNmaCtX0TnTWCMU464RUnVREENNyTtpayk7WragVSGACbCOJKP8EQo11wC7Q61PvLob7PaSsR58sDIOZIOyTbpTiRNKmgOsTaGNIKUKvd9GPJh41JXrWrmftetauZ-0l8HJp3ncjuAd88Vzmr5a5SdYMfTST9ekBq-vSUs9Ye8KgWPjlyxPJepgsOB-Lce2C_98GfwEqmJ62</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>YAO, RUIHONG</creator><creator>SUGINO, ILENE K.</creator><creator>GREULICH, KARIN M.</creator><creator>ISHIDA, MASAHIRO</creator><creator>WEIER, HEINZ-ULRICH G.</creator><creator>ZARBIN, MARCO A.</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>19980201</creationdate><title>Optimization of Non-isotopic in situ Hybridization: Detection of the Y Chromosome in Paraformaldehyde-Fixed, Wax-Embedded Cat Retina</title><author>YAO, RUIHONG ; SUGINO, ILENE K. ; GREULICH, KARIN M. ; ISHIDA, MASAHIRO ; WEIER, HEINZ-ULRICH G. ; ZARBIN, MARCO A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-c21597fd5bca59343b569b69050a84408266b628529e6e35ec7605384e01acde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cats</topic><topic>Cell Nucleus - ultrastructure</topic><topic>DNA - isolation & purification</topic><topic>DNA Probes</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Formaldehyde</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>in situ hybridization</topic><topic>In Situ Hybridization - methods</topic><topic>Male</topic><topic>Paraffin Embedding - methods</topic><topic>Photoreceptor Cells - ultrastructure</topic><topic>photoreceptor transplantation</topic><topic>Pigment Epithelium of Eye - ultrastructure</topic><topic>Polymerase Chain Reaction</topic><topic>Retina</topic><topic>Retina - ultrastructure</topic><topic>retinal pigment epithelial cell transplantation</topic><topic>Staining and Labeling</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Y chromosome</topic><topic>Y Chromosome - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YAO, RUIHONG</creatorcontrib><creatorcontrib>SUGINO, ILENE K.</creatorcontrib><creatorcontrib>GREULICH, KARIN M.</creatorcontrib><creatorcontrib>ISHIDA, MASAHIRO</creatorcontrib><creatorcontrib>WEIER, HEINZ-ULRICH G.</creatorcontrib><creatorcontrib>ZARBIN, MARCO A.</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>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YAO, RUIHONG</au><au>SUGINO, ILENE K.</au><au>GREULICH, KARIN M.</au><au>ISHIDA, MASAHIRO</au><au>WEIER, HEINZ-ULRICH G.</au><au>ZARBIN, MARCO A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimization of Non-isotopic in situ Hybridization: Detection of the Y Chromosome in Paraformaldehyde-Fixed, Wax-Embedded Cat Retina</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>66</volume><issue>2</issue><spage>223</spage><epage>230</epage><pages>223-230</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><coden>EXERA6</coden><abstract>A technique was developed to detect the Y chromosome in paraformaldehyde-fixed diethylglycoldiesterate-embedded cat retina. The Y chromosome specific DNA probe was labeled with digoxigenin through polymerase chain reaction incorporation. After treatment of paraformaldehyde-fixed, diethylglycoldiesterate-embedded tissue sections with deoxyribonucleic acid decondensation and proteolytic digestion, non-fluorescent, non-isotopic in situ hybridization was performed on the retina sections. Most extensive treatment was required for the outer nuclear layer while the inner nuclear layer required more extensive treatment than the retinal pigment epithelial cells. Under optimal pretreatment conditions, the male cat retina displayed black spots which specifically localized at the periphery of the nuclei, while the female cat retina showed negative staining for the Y chromosome specific probe. The technique allows observation of the Y chromosome signal with preservation of retinal morphology and thus may be a valuable tool to discriminate donor cells in retinal pigment epithelial cell and photoreceptor cell transplants.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>9533848</pmid><doi>10.1006/exer.1997.0427</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cats Cell Nucleus - ultrastructure DNA - isolation & purification DNA Probes Eye and associated structures. Visual pathways and centers. Vision Formaldehyde Fundamental and applied biological sciences. Psychology in situ hybridization In Situ Hybridization - methods Male Paraffin Embedding - methods Photoreceptor Cells - ultrastructure photoreceptor transplantation Pigment Epithelium of Eye - ultrastructure Polymerase Chain Reaction Retina Retina - ultrastructure retinal pigment epithelial cell transplantation Staining and Labeling Vertebrates: nervous system and sense organs Y chromosome Y Chromosome - ultrastructure |
title | Optimization of Non-isotopic in situ Hybridization: Detection of the Y Chromosome in Paraformaldehyde-Fixed, Wax-Embedded Cat Retina |
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