Secretory granules of pituitary adenomas : quantitative study of hormonal antigenicity
Ultrastructurally, the antigenicity of major pituitary hormones in secretory granules was quantitatively investigated in five growth hormone (GH)-secreting adenomas, five prolactin (PRL)-secreting adenomas and eight clinically non-functioning (CN-F) adenomas. Sparsely granulated cells with a few or...
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description | Ultrastructurally, the antigenicity of major pituitary hormones in secretory granules was quantitatively investigated in five growth hormone (GH)-secreting adenomas, five prolactin (PRL)-secreting adenomas and eight clinically non-functioning (CN-F) adenomas. Sparsely granulated cells with a few or several small secretory granules (60-100 nm) exhibiting little or only weak antigenicity of various biochemically unrelated hormones were commonly observed in CN-F adenomas and occasionally in GH- and PRL-secreting adenomas. GH- or PRL-secreting adenomas consisted of many densely granulated cells with medium-sized (200-250 nm) or large (over 250 nm) secretory granules and a few or several sparsely granulated cells with small secretory granules. The densely granulated cells showed intense GH or PRL antigenicity and slight to moderate antigenicity for other hormones in large secretory granules and little or only weak antigenicity for various hormones including GH or PRL in small secretory granules. Their secretory granules larger than 160 nm or 140 nm significantly exhibited intense GH or PRL antigenicity (Fisher's exact test; P < 0.05 and < 0.01, respectively). Two CN-F adenomas showed sparsely and densely granulated cells as well as intermediate cells. The densely granulated cells closely resembled GH-secreting cells. The intermediate cells simultaneously included small and medium-sized or large secretory granules exhibiting little/slight and intense GH-antigenicity, respectively. This study indicates that sparsely granulated cells of different categories showing slight antigenicity for various hormones, antigenically share the same origin, and that their hormonality, single or multiple, may be selectively activated in the developmental course of secretory granules. |
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Sparsely granulated cells with a few or several small secretory granules (60-100 nm) exhibiting little or only weak antigenicity of various biochemically unrelated hormones were commonly observed in CN-F adenomas and occasionally in GH- and PRL-secreting adenomas. GH- or PRL-secreting adenomas consisted of many densely granulated cells with medium-sized (200-250 nm) or large (over 250 nm) secretory granules and a few or several sparsely granulated cells with small secretory granules. The densely granulated cells showed intense GH or PRL antigenicity and slight to moderate antigenicity for other hormones in large secretory granules and little or only weak antigenicity for various hormones including GH or PRL in small secretory granules. Their secretory granules larger than 160 nm or 140 nm significantly exhibited intense GH or PRL antigenicity (Fisher's exact test; P < 0.05 and < 0.01, respectively). Two CN-F adenomas showed sparsely and densely granulated cells as well as intermediate cells. The densely granulated cells closely resembled GH-secreting cells. The intermediate cells simultaneously included small and medium-sized or large secretory granules exhibiting little/slight and intense GH-antigenicity, respectively. This study indicates that sparsely granulated cells of different categories showing slight antigenicity for various hormones, antigenically share the same origin, and that their hormonality, single or multiple, may be selectively activated in the developmental course of secretory granules.</description><identifier>ISSN: 0001-6322</identifier><identifier>EISSN: 1432-0533</identifier><identifier>DOI: 10.1007/pl00007436</identifier><identifier>PMID: 10663968</identifier><identifier>CODEN: ANPTAL</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adult ; Aged ; Antigenicity ; Biological and medical sciences ; Endocrinopathies ; Female ; Granule cells ; Growth hormones ; Hormones ; Humans ; Hypothalamus. Hypophysis. Epiphysis (diseases) ; Immunohistochemistry ; Male ; Medical sciences ; Microscopy, Immunoelectron ; Middle Aged ; Non tumoral diseases. Target tissue resistance. Benign neoplasms ; Pituitary ; Pituitary hormones ; Pituitary Hormones - immunology ; Pituitary Neoplasms - immunology ; Pituitary Neoplasms - pathology ; Pituitary Neoplasms - ultrastructure ; Prolactin ; Prolactinoma - immunology ; Prolactinoma - pathology ; Prolactinoma - ultrastructure ; Secretory vesicles ; Tumors</subject><ispartof>Acta neuropathologica, 2000-03, Vol.99 (3), p.263-270</ispartof><rights>2000 INIST-CNRS</rights><rights>Springer-Verlag Berlin Heidelberg 2000.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-8312c000b988fdf98e926e45ea92cad26c9559fc10bbfa8fde6270f9a779b2213</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1257234$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10663968$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KAMITANI, H</creatorcontrib><creatorcontrib>MASUZAWA, H</creatorcontrib><creatorcontrib>KANAZAWA, I</creatorcontrib><creatorcontrib>KUBO, T</creatorcontrib><title>Secretory granules of pituitary adenomas : quantitative study of hormonal antigenicity</title><title>Acta neuropathologica</title><addtitle>Acta Neuropathol</addtitle><description>Ultrastructurally, the antigenicity of major pituitary hormones in secretory granules was quantitatively investigated in five growth hormone (GH)-secreting adenomas, five prolactin (PRL)-secreting adenomas and eight clinically non-functioning (CN-F) adenomas. Sparsely granulated cells with a few or several small secretory granules (60-100 nm) exhibiting little or only weak antigenicity of various biochemically unrelated hormones were commonly observed in CN-F adenomas and occasionally in GH- and PRL-secreting adenomas. GH- or PRL-secreting adenomas consisted of many densely granulated cells with medium-sized (200-250 nm) or large (over 250 nm) secretory granules and a few or several sparsely granulated cells with small secretory granules. The densely granulated cells showed intense GH or PRL antigenicity and slight to moderate antigenicity for other hormones in large secretory granules and little or only weak antigenicity for various hormones including GH or PRL in small secretory granules. Their secretory granules larger than 160 nm or 140 nm significantly exhibited intense GH or PRL antigenicity (Fisher's exact test; P < 0.05 and < 0.01, respectively). Two CN-F adenomas showed sparsely and densely granulated cells as well as intermediate cells. The densely granulated cells closely resembled GH-secreting cells. The intermediate cells simultaneously included small and medium-sized or large secretory granules exhibiting little/slight and intense GH-antigenicity, respectively. This study indicates that sparsely granulated cells of different categories showing slight antigenicity for various hormones, antigenically share the same origin, and that their hormonality, single or multiple, may be selectively activated in the developmental course of secretory granules.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigenicity</subject><subject>Biological and medical sciences</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Granule cells</subject><subject>Growth hormones</subject><subject>Hormones</subject><subject>Humans</subject><subject>Hypothalamus. Hypophysis. Epiphysis (diseases)</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Immunoelectron</subject><subject>Middle Aged</subject><subject>Non tumoral diseases. Target tissue resistance. Benign neoplasms</subject><subject>Pituitary</subject><subject>Pituitary hormones</subject><subject>Pituitary Hormones - immunology</subject><subject>Pituitary Neoplasms - immunology</subject><subject>Pituitary Neoplasms - pathology</subject><subject>Pituitary Neoplasms - ultrastructure</subject><subject>Prolactin</subject><subject>Prolactinoma - immunology</subject><subject>Prolactinoma - pathology</subject><subject>Prolactinoma - ultrastructure</subject><subject>Secretory vesicles</subject><subject>Tumors</subject><issn>0001-6322</issn><issn>1432-0533</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkFtLwzAUx4Mobk5f_ABSUHwQqrm0SeObDG8wUPDyWtI0mRltM3MR9u3N2EQx5yGc__lxOPwAOEbwEkHIrpYdTI8VhO6AMSoIzmFJyC4YpxTllGA8AgfeL1KHWVHugxGClBJOqzF4f1HSqWDdKps7McRO-czqbGlCNEGkVLRqsL3w2XX2GcUQUhrMl8p8iO1qjX5Y19tBdNl6OFeDkSasDsGeFp1XR9t_At7ubl-nD_ns6f5xejPLZQFpyCuCsExXNryqdKt5pTimqiiV4FiKFlPJy5JriWDTaJEQRTGDmgvGeIMxIhNwvtm7dPYzKh_q3nipuk4MykZfM8hhCQlN4Ok_cGGjS2f7GheoZITgVBNwsaGks947peulM33SUCNYr13Xz7Mf1wk-2a6MTa_aP-hGbgLOtoDwUnQ6-ZXG_3K4ZJgU5BuMd4Yt</recordid><startdate>20000301</startdate><enddate>20000301</enddate><creator>KAMITANI, H</creator><creator>MASUZAWA, H</creator><creator>KANAZAWA, I</creator><creator>KUBO, T</creator><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20000301</creationdate><title>Secretory granules of pituitary adenomas : quantitative study of hormonal antigenicity</title><author>KAMITANI, H ; MASUZAWA, H ; KANAZAWA, I ; KUBO, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-8312c000b988fdf98e926e45ea92cad26c9559fc10bbfa8fde6270f9a779b2213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigenicity</topic><topic>Biological and medical sciences</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Granule cells</topic><topic>Growth hormones</topic><topic>Hormones</topic><topic>Humans</topic><topic>Hypothalamus. Hypophysis. Epiphysis (diseases)</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Immunoelectron</topic><topic>Middle Aged</topic><topic>Non tumoral diseases. Target tissue resistance. Benign neoplasms</topic><topic>Pituitary</topic><topic>Pituitary hormones</topic><topic>Pituitary Hormones - immunology</topic><topic>Pituitary Neoplasms - immunology</topic><topic>Pituitary Neoplasms - pathology</topic><topic>Pituitary Neoplasms - ultrastructure</topic><topic>Prolactin</topic><topic>Prolactinoma - immunology</topic><topic>Prolactinoma - pathology</topic><topic>Prolactinoma - ultrastructure</topic><topic>Secretory vesicles</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAMITANI, H</creatorcontrib><creatorcontrib>MASUZAWA, H</creatorcontrib><creatorcontrib>KANAZAWA, I</creatorcontrib><creatorcontrib>KUBO, 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>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Acta neuropathologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAMITANI, H</au><au>MASUZAWA, H</au><au>KANAZAWA, I</au><au>KUBO, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Secretory granules of pituitary adenomas : quantitative study of hormonal antigenicity</atitle><jtitle>Acta neuropathologica</jtitle><addtitle>Acta Neuropathol</addtitle><date>2000-03-01</date><risdate>2000</risdate><volume>99</volume><issue>3</issue><spage>263</spage><epage>270</epage><pages>263-270</pages><issn>0001-6322</issn><eissn>1432-0533</eissn><coden>ANPTAL</coden><abstract>Ultrastructurally, the antigenicity of major pituitary hormones in secretory granules was quantitatively investigated in five growth hormone (GH)-secreting adenomas, five prolactin (PRL)-secreting adenomas and eight clinically non-functioning (CN-F) adenomas. Sparsely granulated cells with a few or several small secretory granules (60-100 nm) exhibiting little or only weak antigenicity of various biochemically unrelated hormones were commonly observed in CN-F adenomas and occasionally in GH- and PRL-secreting adenomas. GH- or PRL-secreting adenomas consisted of many densely granulated cells with medium-sized (200-250 nm) or large (over 250 nm) secretory granules and a few or several sparsely granulated cells with small secretory granules. The densely granulated cells showed intense GH or PRL antigenicity and slight to moderate antigenicity for other hormones in large secretory granules and little or only weak antigenicity for various hormones including GH or PRL in small secretory granules. Their secretory granules larger than 160 nm or 140 nm significantly exhibited intense GH or PRL antigenicity (Fisher's exact test; P < 0.05 and < 0.01, respectively). Two CN-F adenomas showed sparsely and densely granulated cells as well as intermediate cells. The densely granulated cells closely resembled GH-secreting cells. The intermediate cells simultaneously included small and medium-sized or large secretory granules exhibiting little/slight and intense GH-antigenicity, respectively. This study indicates that sparsely granulated cells of different categories showing slight antigenicity for various hormones, antigenically share the same origin, and that their hormonality, single or multiple, may be selectively activated in the developmental course of secretory granules.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>10663968</pmid><doi>10.1007/pl00007436</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Antigenicity Biological and medical sciences Endocrinopathies Female Granule cells Growth hormones Hormones Humans Hypothalamus. Hypophysis. Epiphysis (diseases) Immunohistochemistry Male Medical sciences Microscopy, Immunoelectron Middle Aged Non tumoral diseases. Target tissue resistance. Benign neoplasms Pituitary Pituitary hormones Pituitary Hormones - immunology Pituitary Neoplasms - immunology Pituitary Neoplasms - pathology Pituitary Neoplasms - ultrastructure Prolactin Prolactinoma - immunology Prolactinoma - pathology Prolactinoma - ultrastructure Secretory vesicles Tumors |
title | Secretory granules of pituitary adenomas : quantitative study of hormonal antigenicity |
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