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Immunocytochemical localization of parathormone in the mammalian parathyroid gland using the protein A-gold technique
Electron-microscopic immunocytochemistry for the demonstration of parathormone in parathyroid chief cells was performed in adult male rats, gerbils, mice, and dogs, using the protein A-gold technique. Protein A-gold particles were detected over both large and small secretory granules in all the anim...
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Published in: | Cell and tissue research 1986, Vol.243 (1), p.3-7 |
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description | Electron-microscopic immunocytochemistry for the demonstration of parathormone in parathyroid chief cells was performed in adult male rats, gerbils, mice, and dogs, using the protein A-gold technique. Protein A-gold particles were detected over both large and small secretory granules in all the animals examined. In the former, they were concentrated not only over type-I granules with a large core, but also over type-II granules with a small core. They were also located over atypical granules, including heterogeneously dense granules, granules having vesicles in a finely particulate core, and distorted granules. All labelled secretory granules were characterized by the presence of a clear halo of varying width around the core. Occasionally, Golgi cisternae as well as Golgi vacuoles with a finely particular content were also labelled. The labelling of the secretory granules was strong in dogs, moderate in rats and gerbils, and weak in mice. In addition, it was more intense in the non-osmicated preparations than in the osmicated preparations. The frequency of both types of large granules showed species differences. The possible factors involved in these differences are discussed. |
doi_str_mv | 10.1007/BF00221846 |
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Protein A-gold particles were detected over both large and small secretory granules in all the animals examined. In the former, they were concentrated not only over type-I granules with a large core, but also over type-II granules with a small core. They were also located over atypical granules, including heterogeneously dense granules, granules having vesicles in a finely particulate core, and distorted granules. All labelled secretory granules were characterized by the presence of a clear halo of varying width around the core. Occasionally, Golgi cisternae as well as Golgi vacuoles with a finely particular content were also labelled. The labelling of the secretory granules was strong in dogs, moderate in rats and gerbils, and weak in mice. In addition, it was more intense in the non-osmicated preparations than in the osmicated preparations. The frequency of both types of large granules showed species differences. The possible factors involved in these differences are discussed.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/BF00221846</identifier><identifier>PMID: 2417721</identifier><identifier>CODEN: CTSRCS</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Cytoplasmic Granules - analysis ; Cytoplasmic Granules - ultrastructure ; Dogs ; Fundamental and applied biological sciences. Psychology ; Gerbillinae ; Gold ; Hormones. Regulation ; Immune Sera ; Male ; Mice ; Mice, Inbred Strains ; Microscopy, Electron ; Parathyroid Glands - analysis ; Parathyroid Glands - ultrastructure ; Parathyroid Hormone - analysis ; Rats ; Rats, Inbred Strains ; Species Specificity ; Staining and Labeling - methods ; Staphylococcal Protein A ; Thyroid. Parathyroid. Ultimobranchial body ; Vertebrates: endocrinology</subject><ispartof>Cell and tissue research, 1986, Vol.243 (1), p.3-7</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-50e9595d6c4a24ef482568fc5408e7a53b0f969254cd8eeda368e6357dcb370d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7879159$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2417721$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>INOUE, Y</creatorcontrib><creatorcontrib>SETOGUTI, T</creatorcontrib><title>Immunocytochemical localization of parathormone in the mammalian parathyroid gland using the protein A-gold technique</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>Electron-microscopic immunocytochemistry for the demonstration of parathormone in parathyroid chief cells was performed in adult male rats, gerbils, mice, and dogs, using the protein A-gold technique. Protein A-gold particles were detected over both large and small secretory granules in all the animals examined. In the former, they were concentrated not only over type-I granules with a large core, but also over type-II granules with a small core. They were also located over atypical granules, including heterogeneously dense granules, granules having vesicles in a finely particulate core, and distorted granules. All labelled secretory granules were characterized by the presence of a clear halo of varying width around the core. Occasionally, Golgi cisternae as well as Golgi vacuoles with a finely particular content were also labelled. The labelling of the secretory granules was strong in dogs, moderate in rats and gerbils, and weak in mice. In addition, it was more intense in the non-osmicated preparations than in the osmicated preparations. The frequency of both types of large granules showed species differences. The possible factors involved in these differences are discussed.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cytoplasmic Granules - analysis</subject><subject>Cytoplasmic Granules - ultrastructure</subject><subject>Dogs</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gerbillinae</subject><subject>Gold</subject><subject>Hormones. Regulation</subject><subject>Immune Sera</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microscopy, Electron</subject><subject>Parathyroid Glands - analysis</subject><subject>Parathyroid Glands - ultrastructure</subject><subject>Parathyroid Hormone - analysis</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Species Specificity</subject><subject>Staining and Labeling - methods</subject><subject>Staphylococcal Protein A</subject><subject>Thyroid. Parathyroid. Ultimobranchial body</subject><subject>Vertebrates: endocrinology</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><recordid>eNpFkDtvFDEURq0oKCyBJn0kF1EKpAG_7SmTiECkSDQg0Y289p1dR2N7sWeK5dfHkFFo7i2-cx86CF1Q8okSoj_f3hPCGDVCnaANFZx1xGhzijaEE9ZppX69Re9qfSKECqX6M3TGBNWa0Q1aHmJcUnbHObs9xODshKfcavhj55ATziM-2GLnfS4xJ8Ah4XkPONoYG2TTmh5LDh7vJps8XmpIu3_UoeQZ2sRNt8uTxzO4fQq_F3iP3ox2qvBh7efo5_2XH3ffusfvXx_ubh47xymdO0mgl730ygnLBIzCMKnM6KQgBrSVfEvGXvVMCucNgLdcGVBcau-2XBPPz9H1y972SDtb5yGG6mBqb0Je6tDUGN6MNPDjC-hKrrXAOBxKiLYcB0qGv46H_44bfLluXbYR_Cu6Sm351Zrb2kyOxSYX6iumje6p7PkzVcmFTA</recordid><startdate>1986</startdate><enddate>1986</enddate><creator>INOUE, Y</creator><creator>SETOGUTI, T</creator><general>Springer</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>1986</creationdate><title>Immunocytochemical localization of parathormone in the mammalian parathyroid gland using the protein A-gold technique</title><author>INOUE, Y ; SETOGUTI, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-50e9595d6c4a24ef482568fc5408e7a53b0f969254cd8eeda368e6357dcb370d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cytoplasmic Granules - analysis</topic><topic>Cytoplasmic Granules - ultrastructure</topic><topic>Dogs</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gerbillinae</topic><topic>Gold</topic><topic>Hormones. Regulation</topic><topic>Immune Sera</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microscopy, Electron</topic><topic>Parathyroid Glands - analysis</topic><topic>Parathyroid Glands - ultrastructure</topic><topic>Parathyroid Hormone - analysis</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Species Specificity</topic><topic>Staining and Labeling - methods</topic><topic>Staphylococcal Protein A</topic><topic>Thyroid. Parathyroid. Ultimobranchial body</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>INOUE, Y</creatorcontrib><creatorcontrib>SETOGUTI, 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>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>INOUE, Y</au><au>SETOGUTI, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunocytochemical localization of parathormone in the mammalian parathyroid gland using the protein A-gold technique</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1986</date><risdate>1986</risdate><volume>243</volume><issue>1</issue><spage>3</spage><epage>7</epage><pages>3-7</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><coden>CTSRCS</coden><abstract>Electron-microscopic immunocytochemistry for the demonstration of parathormone in parathyroid chief cells was performed in adult male rats, gerbils, mice, and dogs, using the protein A-gold technique. Protein A-gold particles were detected over both large and small secretory granules in all the animals examined. In the former, they were concentrated not only over type-I granules with a large core, but also over type-II granules with a small core. They were also located over atypical granules, including heterogeneously dense granules, granules having vesicles in a finely particulate core, and distorted granules. All labelled secretory granules were characterized by the presence of a clear halo of varying width around the core. Occasionally, Golgi cisternae as well as Golgi vacuoles with a finely particular content were also labelled. The labelling of the secretory granules was strong in dogs, moderate in rats and gerbils, and weak in mice. In addition, it was more intense in the non-osmicated preparations than in the osmicated preparations. The frequency of both types of large granules showed species differences. The possible factors involved in these differences are discussed.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>2417721</pmid><doi>10.1007/BF00221846</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cytoplasmic Granules - analysis Cytoplasmic Granules - ultrastructure Dogs Fundamental and applied biological sciences. Psychology Gerbillinae Gold Hormones. Regulation Immune Sera Male Mice Mice, Inbred Strains Microscopy, Electron Parathyroid Glands - analysis Parathyroid Glands - ultrastructure Parathyroid Hormone - analysis Rats Rats, Inbred Strains Species Specificity Staining and Labeling - methods Staphylococcal Protein A Thyroid. Parathyroid. Ultimobranchial body Vertebrates: endocrinology |
title | Immunocytochemical localization of parathormone in the mammalian parathyroid gland using the protein A-gold technique |
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