Haemoglobin expression in human endometrium
BACKGROUND The general concept that haemoglobin is only a carrier protein for oxygen and carbon dioxide is challenged since recent studies have shown haemoglobin expression in non-erythroid cells and the protection of haemoglobin against oxidative and nitrosative stress. Using microarrays, we previo...
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Veröffentlicht in: | Human reproduction (Oxford) 2008-03, Vol.23 (3), p.635-641 |
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creator | Dassen, H. Kamps, R. Punyadeera, C. Dijcks, F. de Goeij, A. Ederveen, A. Dunselman, G. Groothuis, P. |
description | BACKGROUND The general concept that haemoglobin is only a carrier protein for oxygen and carbon dioxide is challenged since recent studies have shown haemoglobin expression in non-erythroid cells and the protection of haemoglobin against oxidative and nitrosative stress. Using microarrays, we previously showed expression of haemoglobins α, β, δ and γ and the haeme metabolizing enzyme, haeme oxygenase (HO)-1 in human endometrium. METHODS Using real-time quantitative PCR, haemoglobin α, β, δ and γ, and HO-1 mRNA levels were assessed throughout the menstrual cycle (n = 30 women). Haemoglobin and HO-1 protein levels in the human endometrium were assessed with immunohistochemistry. For steroid responsiveness, menstrual and late proliferative-phase endometrial explants were cultured for 24 h in the presence of vehicle (0.1% ethanol), estradiol (17β-E2, 1 nM), progestin (Org 2058, 1 nM) or 17β-E2+Org 2058 (1 nM each). RESULTS All haemoglobins and the HO-1 were expressed in normal human endometrium. Haemoglobin mRNA and protein expression did not vary significantly during the menstrual cycle. Explant culture with Org 2058 or 17β-E2+Org 2058 increased haemoglobin γ mRNA expression (P < 0.05). HO-1 mRNA levels, and not protein levels, were significantly higher during the menstrual (M)-phase of the cycle (P < 0.05), and were down-regulated by Org 2058 in M-phase explants and by 17β-E2+Org 2058 in LP-phase explants, versus control (P < 0.05). CONCLUSIONS The haemoglobin-HO-1 system may be required to ensure adequate regulation of the bioavailability of haeme, iron and oxygen in human endometrium. |
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Using microarrays, we previously showed expression of haemoglobins α, β, δ and γ and the haeme metabolizing enzyme, haeme oxygenase (HO)-1 in human endometrium. METHODS Using real-time quantitative PCR, haemoglobin α, β, δ and γ, and HO-1 mRNA levels were assessed throughout the menstrual cycle (n = 30 women). Haemoglobin and HO-1 protein levels in the human endometrium were assessed with immunohistochemistry. For steroid responsiveness, menstrual and late proliferative-phase endometrial explants were cultured for 24 h in the presence of vehicle (0.1% ethanol), estradiol (17β-E2, 1 nM), progestin (Org 2058, 1 nM) or 17β-E2+Org 2058 (1 nM each). RESULTS All haemoglobins and the HO-1 were expressed in normal human endometrium. Haemoglobin mRNA and protein expression did not vary significantly during the menstrual cycle. Explant culture with Org 2058 or 17β-E2+Org 2058 increased haemoglobin γ mRNA expression (P < 0.05). HO-1 mRNA levels, and not protein levels, were significantly higher during the menstrual (M)-phase of the cycle (P < 0.05), and were down-regulated by Org 2058 in M-phase explants and by 17β-E2+Org 2058 in LP-phase explants, versus control (P < 0.05). CONCLUSIONS The haemoglobin-HO-1 system may be required to ensure adequate regulation of the bioavailability of haeme, iron and oxygen in human endometrium.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/dem430</identifier><identifier>PMID: 18216035</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Biological and medical sciences ; Endometrium - drug effects ; Endometrium - metabolism ; Estradiol - pharmacology ; Female ; Gynecology. Andrology. Obstetrics ; haeme oxygenase ; haemoglobin ; Heme Oxygenase-1 - biosynthesis ; Hemoglobins - biosynthesis ; human endometrium ; Humans ; Immunohistochemistry ; iron ; Medical sciences ; Menstrual Cycle ; Middle Aged ; Polymerase Chain Reaction ; Pregnenediones - pharmacology ; RNA, Messenger - metabolism ; Tissue Culture Techniques</subject><ispartof>Human reproduction (Oxford), 2008-03, Vol.23 (3), p.635-641</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2008</rights><rights>2008 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-104e5c4238edaf1a9a4ea98c699bdd23d885ae5b21c736747d12cc3da8b4f2b93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20200461$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18216035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dassen, H.</creatorcontrib><creatorcontrib>Kamps, R.</creatorcontrib><creatorcontrib>Punyadeera, C.</creatorcontrib><creatorcontrib>Dijcks, F.</creatorcontrib><creatorcontrib>de Goeij, A.</creatorcontrib><creatorcontrib>Ederveen, A.</creatorcontrib><creatorcontrib>Dunselman, G.</creatorcontrib><creatorcontrib>Groothuis, P.</creatorcontrib><title>Haemoglobin expression in human endometrium</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>BACKGROUND The general concept that haemoglobin is only a carrier protein for oxygen and carbon dioxide is challenged since recent studies have shown haemoglobin expression in non-erythroid cells and the protection of haemoglobin against oxidative and nitrosative stress. Using microarrays, we previously showed expression of haemoglobins α, β, δ and γ and the haeme metabolizing enzyme, haeme oxygenase (HO)-1 in human endometrium. METHODS Using real-time quantitative PCR, haemoglobin α, β, δ and γ, and HO-1 mRNA levels were assessed throughout the menstrual cycle (n = 30 women). Haemoglobin and HO-1 protein levels in the human endometrium were assessed with immunohistochemistry. For steroid responsiveness, menstrual and late proliferative-phase endometrial explants were cultured for 24 h in the presence of vehicle (0.1% ethanol), estradiol (17β-E2, 1 nM), progestin (Org 2058, 1 nM) or 17β-E2+Org 2058 (1 nM each). RESULTS All haemoglobins and the HO-1 were expressed in normal human endometrium. Haemoglobin mRNA and protein expression did not vary significantly during the menstrual cycle. Explant culture with Org 2058 or 17β-E2+Org 2058 increased haemoglobin γ mRNA expression (P < 0.05). HO-1 mRNA levels, and not protein levels, were significantly higher during the menstrual (M)-phase of the cycle (P < 0.05), and were down-regulated by Org 2058 in M-phase explants and by 17β-E2+Org 2058 in LP-phase explants, versus control (P < 0.05). CONCLUSIONS The haemoglobin-HO-1 system may be required to ensure adequate regulation of the bioavailability of haeme, iron and oxygen in human endometrium.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Endometrium - drug effects</subject><subject>Endometrium - metabolism</subject><subject>Estradiol - pharmacology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>haeme oxygenase</subject><subject>haemoglobin</subject><subject>Heme Oxygenase-1 - biosynthesis</subject><subject>Hemoglobins - biosynthesis</subject><subject>human endometrium</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>iron</subject><subject>Medical sciences</subject><subject>Menstrual Cycle</subject><subject>Middle Aged</subject><subject>Polymerase Chain Reaction</subject><subject>Pregnenediones - pharmacology</subject><subject>RNA, Messenger - metabolism</subject><subject>Tissue Culture Techniques</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0N1L3jAUB-AgG_pOvdztkIFjMKo5SZomlyq6d6DI2AbiTUiT062ubWryFvS_N9LiYDde5YOH8_Ej5D3QI6CaH_-Z-ojjscdecLpFViAkLRgv6RuyokyqAkDCDnmX0h2l-arkNtkBxUBSXq7Il7XFPvzuQt0OB_gwRkypDcNBfuXKNv8NPvS4ie3U75G3je0S7i_nLvl1cf7zbF1cXn_9dnZyWTih9KYAKrB0gnGF3jZgtRVotXJS69p7xr1SpcWyZuAqLitReWDOcW9VLRpWa75LPs11xxjuJ0wb07fJYdfZAcOUTEW50CXwVyGjpcirVhl-_A_ehSkOeQnDALTQwCGjYkYuhpQiNmaMbW_jowFqnrM2c9Zmzjr7D0vRqe7R_9NLuBkcLsAmZ7sm2sG16cUxyigV8rnx59mFaXy15zJjmzb48IJt_GtkxavSrG9uzen69juHH1fmlD8B_rGkzA</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Dassen, H.</creator><creator>Kamps, R.</creator><creator>Punyadeera, C.</creator><creator>Dijcks, F.</creator><creator>de Goeij, A.</creator><creator>Ederveen, A.</creator><creator>Dunselman, G.</creator><creator>Groothuis, P.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20080301</creationdate><title>Haemoglobin expression in human endometrium</title><author>Dassen, H. ; Kamps, R. ; Punyadeera, C. ; Dijcks, F. ; de Goeij, A. ; Ederveen, A. ; Dunselman, G. ; Groothuis, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-104e5c4238edaf1a9a4ea98c699bdd23d885ae5b21c736747d12cc3da8b4f2b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Endometrium - drug effects</topic><topic>Endometrium - metabolism</topic><topic>Estradiol - pharmacology</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>haeme oxygenase</topic><topic>haemoglobin</topic><topic>Heme Oxygenase-1 - biosynthesis</topic><topic>Hemoglobins - biosynthesis</topic><topic>human endometrium</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>iron</topic><topic>Medical sciences</topic><topic>Menstrual Cycle</topic><topic>Middle Aged</topic><topic>Polymerase Chain Reaction</topic><topic>Pregnenediones - pharmacology</topic><topic>RNA, Messenger - metabolism</topic><topic>Tissue Culture Techniques</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dassen, H.</creatorcontrib><creatorcontrib>Kamps, R.</creatorcontrib><creatorcontrib>Punyadeera, C.</creatorcontrib><creatorcontrib>Dijcks, F.</creatorcontrib><creatorcontrib>de Goeij, A.</creatorcontrib><creatorcontrib>Ederveen, A.</creatorcontrib><creatorcontrib>Dunselman, G.</creatorcontrib><creatorcontrib>Groothuis, P.</creatorcontrib><collection>Istex</collection><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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dassen, H.</au><au>Kamps, R.</au><au>Punyadeera, C.</au><au>Dijcks, F.</au><au>de Goeij, A.</au><au>Ederveen, A.</au><au>Dunselman, G.</au><au>Groothuis, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Haemoglobin expression in human endometrium</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>23</volume><issue>3</issue><spage>635</spage><epage>641</epage><pages>635-641</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND The general concept that haemoglobin is only a carrier protein for oxygen and carbon dioxide is challenged since recent studies have shown haemoglobin expression in non-erythroid cells and the protection of haemoglobin against oxidative and nitrosative stress. Using microarrays, we previously showed expression of haemoglobins α, β, δ and γ and the haeme metabolizing enzyme, haeme oxygenase (HO)-1 in human endometrium. METHODS Using real-time quantitative PCR, haemoglobin α, β, δ and γ, and HO-1 mRNA levels were assessed throughout the menstrual cycle (n = 30 women). Haemoglobin and HO-1 protein levels in the human endometrium were assessed with immunohistochemistry. For steroid responsiveness, menstrual and late proliferative-phase endometrial explants were cultured for 24 h in the presence of vehicle (0.1% ethanol), estradiol (17β-E2, 1 nM), progestin (Org 2058, 1 nM) or 17β-E2+Org 2058 (1 nM each). RESULTS All haemoglobins and the HO-1 were expressed in normal human endometrium. Haemoglobin mRNA and protein expression did not vary significantly during the menstrual cycle. Explant culture with Org 2058 or 17β-E2+Org 2058 increased haemoglobin γ mRNA expression (P < 0.05). HO-1 mRNA levels, and not protein levels, were significantly higher during the menstrual (M)-phase of the cycle (P < 0.05), and were down-regulated by Org 2058 in M-phase explants and by 17β-E2+Org 2058 in LP-phase explants, versus control (P < 0.05). CONCLUSIONS The haemoglobin-HO-1 system may be required to ensure adequate regulation of the bioavailability of haeme, iron and oxygen in human endometrium.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18216035</pmid><doi>10.1093/humrep/dem430</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences Endometrium - drug effects Endometrium - metabolism Estradiol - pharmacology Female Gynecology. Andrology. Obstetrics haeme oxygenase haemoglobin Heme Oxygenase-1 - biosynthesis Hemoglobins - biosynthesis human endometrium Humans Immunohistochemistry iron Medical sciences Menstrual Cycle Middle Aged Polymerase Chain Reaction Pregnenediones - pharmacology RNA, Messenger - metabolism Tissue Culture Techniques |
title | Haemoglobin expression in human endometrium |
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