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Clock Gene Expression in the Human Pituitary Gland
Pituitary function relies on strictly timed, yet plastic mechanisms, particularly with respect to the daytime-dependent coordination of hormone synthesis and release. In other systems, clock genes and their protein products are well-described candidates to anticipate the daily demands in neuroendocr...
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Published in: | Endocrinology (Philadelphia) 2013-06, Vol.154 (6), p.2046-2057 |
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creator | Wunderer, Florian Kühne, Sina Jilg, Antje Ackermann, Katrin Sebesteny, Tamas Maronde, Erik Stehle, Jörg H |
description | Pituitary function relies on strictly timed, yet plastic mechanisms, particularly with respect to the daytime-dependent coordination of hormone synthesis and release. In other systems, clock genes and their protein products are well-described candidates to anticipate the daily demands in neuroendocrine coupling and to manage cellular adaptation on changing internal or external circumstances. To elucidate possible mechanisms of time management, a total of 52 human autoptic pituitary glands were allocated to the 4 time-of-day groups, night, dawn, day, and dusk, according to reported time of death. The observed daytime-dependent dynamics in ACTH content supports a postmortem conservation of the premortem condition, and thus, principally validates the investigation of autoptic pituitary glands. Pituitary extracts were investigated for expression of clock genes Per1, Cry1, Clock, and Bmal1 and corresponding protein products. Only the clock gene Per1 showed daytime-dependent differences in quantitative real-time PCR analyses, with decreased levels observed during dusk. Although the overall amount in clock gene protein products PER1, CRY1, and CLOCK did not fluctuate with time of day in human pituitary, an indication for a temporally parallel intracellular translocation of PER1 and CRY1 was detected by immunofluorescence. Presented data suggest that the observed clock gene expression in human pituitary cells does not provide evidence for a functional intrinsic clockwork. It is suggested that clock genes and their protein products may be directly involved in the daytime-dependent regulation and adaptation of hormone synthesis and release and within homeostatic adaptive plasticity. |
doi_str_mv | 10.1210/en.2012-2274 |
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In other systems, clock genes and their protein products are well-described candidates to anticipate the daily demands in neuroendocrine coupling and to manage cellular adaptation on changing internal or external circumstances. To elucidate possible mechanisms of time management, a total of 52 human autoptic pituitary glands were allocated to the 4 time-of-day groups, night, dawn, day, and dusk, according to reported time of death. The observed daytime-dependent dynamics in ACTH content supports a postmortem conservation of the premortem condition, and thus, principally validates the investigation of autoptic pituitary glands. Pituitary extracts were investigated for expression of clock genes Per1, Cry1, Clock, and Bmal1 and corresponding protein products. Only the clock gene Per1 showed daytime-dependent differences in quantitative real-time PCR analyses, with decreased levels observed during dusk. Although the overall amount in clock gene protein products PER1, CRY1, and CLOCK did not fluctuate with time of day in human pituitary, an indication for a temporally parallel intracellular translocation of PER1 and CRY1 was detected by immunofluorescence. Presented data suggest that the observed clock gene expression in human pituitary cells does not provide evidence for a functional intrinsic clockwork. It is suggested that clock genes and their protein products may be directly involved in the daytime-dependent regulation and adaptation of hormone synthesis and release and within homeostatic adaptive plasticity.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2012-2274</identifier><identifier>PMID: 23584858</identifier><identifier>CODEN: ENDOAO</identifier><language>eng</language><publisher>Chevy Chase, MD: Endocrine Society</publisher><subject>Adaptation ; Adolescent ; Adrenocorticotropic hormone ; Adrenocorticotropic Hormone - metabolism ; Adult ; Aged ; Aged, 80 and over ; ARNTL Transcription Factors - genetics ; ARNTL Transcription Factors - metabolism ; Autopsy ; Biological and medical sciences ; Blotting, Western ; BMAL1 protein ; Child ; Chronobiology ; Circadian Rhythm ; Clock gene ; CLOCK Proteins - genetics ; CLOCK Proteins - metabolism ; Cryptochromes ; Cryptochromes - genetics ; Cryptochromes - metabolism ; Daytime ; Female ; Functional plasticity ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Gene Expression - radiation effects ; Gene regulation ; Genes ; Homeostatic plasticity ; Humans ; Immunofluorescence ; Immunohistochemistry ; Male ; Middle Aged ; Period 1 protein ; Period Circadian Proteins - genetics ; Period Circadian Proteins - metabolism ; Pituitary ; Pituitary gland ; Pituitary Gland - metabolism ; Pituitary Gland - radiation effects ; Plastic foam ; Postmortem Changes ; Protein biosynthesis ; Protein transport ; Proteins ; Real time ; Reverse Transcriptase Polymerase Chain Reaction ; Synthesis ; Time dependence ; Time management ; Time of use ; Translocation ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: endocrinology ; Young Adult</subject><ispartof>Endocrinology (Philadelphia), 2013-06, Vol.154 (6), p.2046-2057</ispartof><rights>Copyright © 2013 by The Endocrine Society</rights><rights>Copyright © 2013 by The Endocrine Society 2013</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-a1972f8b38c04ed76440256b8bba27e2555893a591487a8eec98a89794228fd43</citedby><cites>FETCH-LOGICAL-c562t-a1972f8b38c04ed76440256b8bba27e2555893a591487a8eec98a89794228fd43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27363716$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23584858$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wunderer, Florian</creatorcontrib><creatorcontrib>Kühne, Sina</creatorcontrib><creatorcontrib>Jilg, Antje</creatorcontrib><creatorcontrib>Ackermann, Katrin</creatorcontrib><creatorcontrib>Sebesteny, Tamas</creatorcontrib><creatorcontrib>Maronde, Erik</creatorcontrib><creatorcontrib>Stehle, Jörg H</creatorcontrib><title>Clock Gene Expression in the Human Pituitary Gland</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Pituitary function relies on strictly timed, yet plastic mechanisms, particularly with respect to the daytime-dependent coordination of hormone synthesis and release. In other systems, clock genes and their protein products are well-described candidates to anticipate the daily demands in neuroendocrine coupling and to manage cellular adaptation on changing internal or external circumstances. To elucidate possible mechanisms of time management, a total of 52 human autoptic pituitary glands were allocated to the 4 time-of-day groups, night, dawn, day, and dusk, according to reported time of death. The observed daytime-dependent dynamics in ACTH content supports a postmortem conservation of the premortem condition, and thus, principally validates the investigation of autoptic pituitary glands. Pituitary extracts were investigated for expression of clock genes Per1, Cry1, Clock, and Bmal1 and corresponding protein products. Only the clock gene Per1 showed daytime-dependent differences in quantitative real-time PCR analyses, with decreased levels observed during dusk. Although the overall amount in clock gene protein products PER1, CRY1, and CLOCK did not fluctuate with time of day in human pituitary, an indication for a temporally parallel intracellular translocation of PER1 and CRY1 was detected by immunofluorescence. Presented data suggest that the observed clock gene expression in human pituitary cells does not provide evidence for a functional intrinsic clockwork. It is suggested that clock genes and their protein products may be directly involved in the daytime-dependent regulation and adaptation of hormone synthesis and release and within homeostatic adaptive plasticity.</description><subject>Adaptation</subject><subject>Adolescent</subject><subject>Adrenocorticotropic hormone</subject><subject>Adrenocorticotropic Hormone - metabolism</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>ARNTL Transcription Factors - genetics</subject><subject>ARNTL Transcription Factors - metabolism</subject><subject>Autopsy</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>BMAL1 protein</subject><subject>Child</subject><subject>Chronobiology</subject><subject>Circadian Rhythm</subject><subject>Clock gene</subject><subject>CLOCK Proteins - genetics</subject><subject>CLOCK Proteins - metabolism</subject><subject>Cryptochromes</subject><subject>Cryptochromes - genetics</subject><subject>Cryptochromes - metabolism</subject><subject>Daytime</subject><subject>Female</subject><subject>Functional plasticity</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression - radiation effects</subject><subject>Gene regulation</subject><subject>Genes</subject><subject>Homeostatic plasticity</subject><subject>Humans</subject><subject>Immunofluorescence</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Period 1 protein</subject><subject>Period Circadian Proteins - genetics</subject><subject>Period Circadian Proteins - metabolism</subject><subject>Pituitary</subject><subject>Pituitary gland</subject><subject>Pituitary Gland - metabolism</subject><subject>Pituitary Gland - radiation effects</subject><subject>Plastic foam</subject><subject>Postmortem Changes</subject><subject>Protein biosynthesis</subject><subject>Protein transport</subject><subject>Proteins</subject><subject>Real time</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Synthesis</subject><subject>Time dependence</subject><subject>Time management</subject><subject>Time of use</subject><subject>Translocation</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: endocrinology</subject><subject>Young Adult</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqF0U1LwzAYB_Agis6Xm2cpiOjBat6THmXMKQh60HNI06dY7dKZtKDf3sxNBVE8hZAfz8s_CO0TfEYowefgzygmNKdU8TU0IgUXuSIKr6MRxoTlKj1soe0Yn9KVc8420RZlQnMt9AjRcdu552wKHrLJ6zxAjE3ns8Zn_SNkV8PM-uyu6Yemt-Etm7bWV7too7ZthL3VuYMeLif346v85nZ6Pb64yZ2QtM8tKRStdcm0wxwqJTnHVMhSl6WlCqgQQhfMioJwrawGcIW2ulAFp1TXFWc76GRZdx66lwFib2ZNdNCmGaAboiFSYo41Y-p_ygTjSqqCJXr4gz51Q_BpEcMIwzKlpRbqdKlc6GIMUJt5aGYpAkOwWcRuwJtF7GYRe-IHq6JDOYPqC3_mnMDRCtjobFsH610Tv51ikikikzteum6Y_9UyX7VkSwm-6lxoPHx83vc2vw76DqOtotM</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Wunderer, Florian</creator><creator>Kühne, Sina</creator><creator>Jilg, Antje</creator><creator>Ackermann, Katrin</creator><creator>Sebesteny, Tamas</creator><creator>Maronde, Erik</creator><creator>Stehle, Jörg H</creator><general>Endocrine Society</general><general>Oxford University Press</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>RC3</scope></search><sort><creationdate>20130601</creationdate><title>Clock Gene Expression in the Human Pituitary Gland</title><author>Wunderer, Florian ; Kühne, Sina ; Jilg, Antje ; Ackermann, Katrin ; Sebesteny, Tamas ; Maronde, Erik ; Stehle, Jörg H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-a1972f8b38c04ed76440256b8bba27e2555893a591487a8eec98a89794228fd43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adaptation</topic><topic>Adolescent</topic><topic>Adrenocorticotropic hormone</topic><topic>Adrenocorticotropic Hormone - metabolism</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>ARNTL Transcription Factors - genetics</topic><topic>ARNTL Transcription Factors - metabolism</topic><topic>Autopsy</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>BMAL1 protein</topic><topic>Child</topic><topic>Chronobiology</topic><topic>Circadian Rhythm</topic><topic>Clock gene</topic><topic>CLOCK Proteins - genetics</topic><topic>CLOCK Proteins - metabolism</topic><topic>Cryptochromes</topic><topic>Cryptochromes - genetics</topic><topic>Cryptochromes - metabolism</topic><topic>Daytime</topic><topic>Female</topic><topic>Functional plasticity</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene expression</topic><topic>Gene Expression - radiation effects</topic><topic>Gene regulation</topic><topic>Genes</topic><topic>Homeostatic plasticity</topic><topic>Humans</topic><topic>Immunofluorescence</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Period 1 protein</topic><topic>Period Circadian Proteins - genetics</topic><topic>Period Circadian Proteins - metabolism</topic><topic>Pituitary</topic><topic>Pituitary gland</topic><topic>Pituitary Gland - metabolism</topic><topic>Pituitary Gland - radiation effects</topic><topic>Plastic foam</topic><topic>Postmortem Changes</topic><topic>Protein biosynthesis</topic><topic>Protein transport</topic><topic>Proteins</topic><topic>Real time</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Synthesis</topic><topic>Time dependence</topic><topic>Time management</topic><topic>Time of use</topic><topic>Translocation</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: endocrinology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wunderer, Florian</creatorcontrib><creatorcontrib>Kühne, Sina</creatorcontrib><creatorcontrib>Jilg, Antje</creatorcontrib><creatorcontrib>Ackermann, Katrin</creatorcontrib><creatorcontrib>Sebesteny, Tamas</creatorcontrib><creatorcontrib>Maronde, Erik</creatorcontrib><creatorcontrib>Stehle, Jörg H</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>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Genetics Abstracts</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wunderer, Florian</au><au>Kühne, Sina</au><au>Jilg, Antje</au><au>Ackermann, Katrin</au><au>Sebesteny, Tamas</au><au>Maronde, Erik</au><au>Stehle, Jörg H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clock Gene Expression in the Human Pituitary Gland</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>154</volume><issue>6</issue><spage>2046</spage><epage>2057</epage><pages>2046-2057</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><coden>ENDOAO</coden><abstract>Pituitary function relies on strictly timed, yet plastic mechanisms, particularly with respect to the daytime-dependent coordination of hormone synthesis and release. In other systems, clock genes and their protein products are well-described candidates to anticipate the daily demands in neuroendocrine coupling and to manage cellular adaptation on changing internal or external circumstances. To elucidate possible mechanisms of time management, a total of 52 human autoptic pituitary glands were allocated to the 4 time-of-day groups, night, dawn, day, and dusk, according to reported time of death. The observed daytime-dependent dynamics in ACTH content supports a postmortem conservation of the premortem condition, and thus, principally validates the investigation of autoptic pituitary glands. Pituitary extracts were investigated for expression of clock genes Per1, Cry1, Clock, and Bmal1 and corresponding protein products. Only the clock gene Per1 showed daytime-dependent differences in quantitative real-time PCR analyses, with decreased levels observed during dusk. Although the overall amount in clock gene protein products PER1, CRY1, and CLOCK did not fluctuate with time of day in human pituitary, an indication for a temporally parallel intracellular translocation of PER1 and CRY1 was detected by immunofluorescence. Presented data suggest that the observed clock gene expression in human pituitary cells does not provide evidence for a functional intrinsic clockwork. It is suggested that clock genes and their protein products may be directly involved in the daytime-dependent regulation and adaptation of hormone synthesis and release and within homeostatic adaptive plasticity.</abstract><cop>Chevy Chase, MD</cop><pub>Endocrine Society</pub><pmid>23584858</pmid><doi>10.1210/en.2012-2274</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation Adolescent Adrenocorticotropic hormone Adrenocorticotropic Hormone - metabolism Adult Aged Aged, 80 and over ARNTL Transcription Factors - genetics ARNTL Transcription Factors - metabolism Autopsy Biological and medical sciences Blotting, Western BMAL1 protein Child Chronobiology Circadian Rhythm Clock gene CLOCK Proteins - genetics CLOCK Proteins - metabolism Cryptochromes Cryptochromes - genetics Cryptochromes - metabolism Daytime Female Functional plasticity Fundamental and applied biological sciences. Psychology Gene expression Gene Expression - radiation effects Gene regulation Genes Homeostatic plasticity Humans Immunofluorescence Immunohistochemistry Male Middle Aged Period 1 protein Period Circadian Proteins - genetics Period Circadian Proteins - metabolism Pituitary Pituitary gland Pituitary Gland - metabolism Pituitary Gland - radiation effects Plastic foam Postmortem Changes Protein biosynthesis Protein transport Proteins Real time Reverse Transcriptase Polymerase Chain Reaction Synthesis Time dependence Time management Time of use Translocation Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: endocrinology Young Adult |
title | Clock Gene Expression in the Human Pituitary Gland |
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