Differential expression and regulation of thyrotropin (TSH) in T cell lines
The immune system's production of and response to thyrotropin (TSH) suggests the existence of a hypothalamic-lymphoid-thyroid regulatory axis (HLT). To evaluate the possible roles of lymphocyte-derived TSH we characterized its structure and regulation of production. Using an in vitro system, we...
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Veröffentlicht in: | Molecular and cellular endocrinology 1989-07, Vol.64 (2), p.229-241 |
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description | The immune system's production of and response to thyrotropin (TSH) suggests the existence of a hypothalamic-lymphoid-thyroid regulatory axis (HLT). To evaluate the possible roles of lymphocyte-derived TSH we characterized its structure and regulation of production. Using an in vitro system, we screened T cell lines for the production of TSH in response to thyrotropin-releasing hormone (TRH). We identified MOLT 4 T cells as producers of intact TSH based on TSH radioimmunoassay (RIA) displacement and de novo synthesized protein structure similar to pituitary TSH. Northern blot analysis using a cDNA probe to TSHβ showed the existence of an mRNA species similar in molecular size to pituitary mRNA of TSHβ. The MOLT 4-derived TSH is induced in a dose-dependent fashion by TRH and that induction is significantly inhibited by the thyroid hormone, triiodothyronine (T
3). HUT 78 T cells express an mRNA species similar to TSHβ but do not express detectable protein suggesting a lack of translation of the mRNA species. The evidence suggests that the MOLT 4 T cells serve as an in vitro model for TSH production and may be used to study differential expression of the genes for TSH in the immune system. Elucidation of this in vitro system will provide information on mechanisms of regulation of an HLT axis that are unique to the immune system as well as pathways common to the immune and neuroendocrine systems. |
doi_str_mv | 10.1016/0303-7207(89)90150-0 |
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3). HUT 78 T cells express an mRNA species similar to TSHβ but do not express detectable protein suggesting a lack of translation of the mRNA species. The evidence suggests that the MOLT 4 T cells serve as an in vitro model for TSH production and may be used to study differential expression of the genes for TSH in the immune system. Elucidation of this in vitro system will provide information on mechanisms of regulation of an HLT axis that are unique to the immune system as well as pathways common to the immune and neuroendocrine systems.</description><identifier>ISSN: 0303-7207</identifier><identifier>EISSN: 1872-8057</identifier><identifier>DOI: 10.1016/0303-7207(89)90150-0</identifier><identifier>PMID: 2507375</identifier><identifier>CODEN: MCEND6</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Biological and medical sciences ; Cell Line ; Chromatography, High Pressure Liquid ; Electrophoresis, Polyacrylamide Gel ; Enzyme-Linked Immunosorbent Assay ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression Regulation ; Hemolytic Plaque Technique ; Humans ; Lymphocyte-derived thyrotropin ; Molecular and cellular biology ; Molecular genetics ; Molecular Weight ; Radioimmunoassay ; RNA, Messenger - metabolism ; T-Lymphocytes - physiology ; Thyrotropin - biosynthesis ; Thyrotropin - genetics ; Thyrotropin gene expression ; Thyrotropin regulation ; Thyrotropin-Releasing Hormone - physiology</subject><ispartof>Molecular and cellular endocrinology, 1989-07, Vol.64 (2), p.229-241</ispartof><rights>1989</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-ca624add067a7cefbdbf8daf4fa007faea38ed4cb5849676291788b7944392013</citedby><cites>FETCH-LOGICAL-c417t-ca624add067a7cefbdbf8daf4fa007faea38ed4cb5849676291788b7944392013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0303-7207(89)90150-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6786438$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2507375$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harbour, Deborah V.</creatorcontrib><creatorcontrib>Kruger, Thomas E.</creatorcontrib><creatorcontrib>Coppenhaver, Dorian</creatorcontrib><creatorcontrib>Smith, Eric M.</creatorcontrib><creatorcontrib>Meyer, Walter J.</creatorcontrib><title>Differential expression and regulation of thyrotropin (TSH) in T cell lines</title><title>Molecular and cellular endocrinology</title><addtitle>Mol Cell Endocrinol</addtitle><description>The immune system's production of and response to thyrotropin (TSH) suggests the existence of a hypothalamic-lymphoid-thyroid regulatory axis (HLT). To evaluate the possible roles of lymphocyte-derived TSH we characterized its structure and regulation of production. Using an in vitro system, we screened T cell lines for the production of TSH in response to thyrotropin-releasing hormone (TRH). We identified MOLT 4 T cells as producers of intact TSH based on TSH radioimmunoassay (RIA) displacement and de novo synthesized protein structure similar to pituitary TSH. Northern blot analysis using a cDNA probe to TSHβ showed the existence of an mRNA species similar in molecular size to pituitary mRNA of TSHβ. The MOLT 4-derived TSH is induced in a dose-dependent fashion by TRH and that induction is significantly inhibited by the thyroid hormone, triiodothyronine (T
3). HUT 78 T cells express an mRNA species similar to TSHβ but do not express detectable protein suggesting a lack of translation of the mRNA species. The evidence suggests that the MOLT 4 T cells serve as an in vitro model for TSH production and may be used to study differential expression of the genes for TSH in the immune system. Elucidation of this in vitro system will provide information on mechanisms of regulation of an HLT axis that are unique to the immune system as well as pathways common to the immune and neuroendocrine systems.</description><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Hemolytic Plaque Technique</subject><subject>Humans</subject><subject>Lymphocyte-derived thyrotropin</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Weight</subject><subject>Radioimmunoassay</subject><subject>RNA, Messenger - metabolism</subject><subject>T-Lymphocytes - physiology</subject><subject>Thyrotropin - biosynthesis</subject><subject>Thyrotropin - genetics</subject><subject>Thyrotropin gene expression</subject><subject>Thyrotropin regulation</subject><subject>Thyrotropin-Releasing Hormone - physiology</subject><issn>0303-7207</issn><issn>1872-8057</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAQhoMo6_rxDxR6EHEP1UmTNulFEL9R8OB6Dmky0Ui3XZOu6L-3dZc96mlmmGeGl4eQAwqnFGhxBgxYKjIQJ7KclEBzSGGDjKkUWSohF5tkvEa2yU6M7wAg8kyOyCjLQTCRj8nDlXcOAzad13WCX_OAMfq2SXRjk4Cvi1p3w9i6pHv7Dm0X2rlvkpPp890k6ZtpYrCuk9o3GPfIltN1xP1V3SUvN9fTy7v08en2_vLiMTWcii41usi4thYKoYVBV9nKSasdd7rP5zRqJtFyU-WSl4UospIKKStRcs7KDCjbJcfLv_PQfiwwdmrm4xBDN9guohJlxiiw_0Gac5ZzCT3Il6AJbYwBnZoHP9PhW1FQg2w1mFSDSSVL9StbDWeHq_-LaoZ2fbSy2--PVnsdja5d0I3xcY0VQhacyR47X2LYS_v0GFQ0HhuD1gc0nbKt_zvHDyTpmfY</recordid><startdate>19890701</startdate><enddate>19890701</enddate><creator>Harbour, Deborah V.</creator><creator>Kruger, Thomas E.</creator><creator>Coppenhaver, Dorian</creator><creator>Smith, Eric M.</creator><creator>Meyer, Walter J.</creator><general>Elsevier Ireland 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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19890701</creationdate><title>Differential expression and regulation of thyrotropin (TSH) in T cell lines</title><author>Harbour, Deborah V. ; Kruger, Thomas E. ; Coppenhaver, Dorian ; Smith, Eric M. ; Meyer, Walter J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-ca624add067a7cefbdbf8daf4fa007faea38ed4cb5849676291788b7944392013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Hemolytic Plaque Technique</topic><topic>Humans</topic><topic>Lymphocyte-derived thyrotropin</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Weight</topic><topic>Radioimmunoassay</topic><topic>RNA, Messenger - metabolism</topic><topic>T-Lymphocytes - physiology</topic><topic>Thyrotropin - biosynthesis</topic><topic>Thyrotropin - genetics</topic><topic>Thyrotropin gene expression</topic><topic>Thyrotropin regulation</topic><topic>Thyrotropin-Releasing Hormone - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harbour, Deborah V.</creatorcontrib><creatorcontrib>Kruger, Thomas E.</creatorcontrib><creatorcontrib>Coppenhaver, Dorian</creatorcontrib><creatorcontrib>Smith, Eric M.</creatorcontrib><creatorcontrib>Meyer, Walter J.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harbour, Deborah V.</au><au>Kruger, Thomas E.</au><au>Coppenhaver, Dorian</au><au>Smith, Eric M.</au><au>Meyer, Walter J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression and regulation of thyrotropin (TSH) in T cell lines</atitle><jtitle>Molecular and cellular endocrinology</jtitle><addtitle>Mol Cell Endocrinol</addtitle><date>1989-07-01</date><risdate>1989</risdate><volume>64</volume><issue>2</issue><spage>229</spage><epage>241</epage><pages>229-241</pages><issn>0303-7207</issn><eissn>1872-8057</eissn><coden>MCEND6</coden><abstract>The immune system's production of and response to thyrotropin (TSH) suggests the existence of a hypothalamic-lymphoid-thyroid regulatory axis (HLT). To evaluate the possible roles of lymphocyte-derived TSH we characterized its structure and regulation of production. Using an in vitro system, we screened T cell lines for the production of TSH in response to thyrotropin-releasing hormone (TRH). We identified MOLT 4 T cells as producers of intact TSH based on TSH radioimmunoassay (RIA) displacement and de novo synthesized protein structure similar to pituitary TSH. Northern blot analysis using a cDNA probe to TSHβ showed the existence of an mRNA species similar in molecular size to pituitary mRNA of TSHβ. The MOLT 4-derived TSH is induced in a dose-dependent fashion by TRH and that induction is significantly inhibited by the thyroid hormone, triiodothyronine (T
3). HUT 78 T cells express an mRNA species similar to TSHβ but do not express detectable protein suggesting a lack of translation of the mRNA species. The evidence suggests that the MOLT 4 T cells serve as an in vitro model for TSH production and may be used to study differential expression of the genes for TSH in the immune system. Elucidation of this in vitro system will provide information on mechanisms of regulation of an HLT axis that are unique to the immune system as well as pathways common to the immune and neuroendocrine systems.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>2507375</pmid><doi>10.1016/0303-7207(89)90150-0</doi><tpages>13</tpages></addata></record> |
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subjects | Biological and medical sciences Cell Line Chromatography, High Pressure Liquid Electrophoresis, Polyacrylamide Gel Enzyme-Linked Immunosorbent Assay Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology Gene expression Gene Expression Regulation Hemolytic Plaque Technique Humans Lymphocyte-derived thyrotropin Molecular and cellular biology Molecular genetics Molecular Weight Radioimmunoassay RNA, Messenger - metabolism T-Lymphocytes - physiology Thyrotropin - biosynthesis Thyrotropin - genetics Thyrotropin gene expression Thyrotropin regulation Thyrotropin-Releasing Hormone - physiology |
title | Differential expression and regulation of thyrotropin (TSH) in T cell lines |
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