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Relaxin-Like Factor Expression as a Marker of Differentiation in the Mouse Testis and Ovary
Abstract Expression of the relaxin-like factor (RLF) was studied at the messenger RNA (mRNA) and protein levels in the testes and ovaries of the mouse, as well as through testicular development and differentiation in the mouse testis. In situ hybridization or RT-PCR, and immunohistochemistry using a...
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Published in: | Endocrinology (Philadelphia) 1998-06, Vol.139 (6), p.2960-2970 |
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container_title | Endocrinology (Philadelphia) |
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creator | Balvers, M. Spiess, A.-N. Domagalski, R. Hunt, N. Kilic, E. Mukhopadhyay, A. K. Hanks, E. Charlton, H. M. Ivell, R. |
description | Abstract
Expression of the relaxin-like factor (RLF) was studied at the messenger RNA (mRNA) and protein levels in the testes and ovaries of the mouse, as well as through testicular development and differentiation in the mouse testis. In situ hybridization or RT-PCR, and immunohistochemistry using a polyclonal antibody raised against a recombinant protein, provided mutually confirmatory results for a high expression of RLF in the Leydig cells of the adult testis and at a much lower level of expression in the luteal cells of the ovary through the cycle, pregnancy, and in lactation. Analysis of protein and mRNA expression, through postnatal testicular development, indicated moderate RLF expression also in the fetal population of Leydig cells, even in the hpg mutant mouse, lacking an active pituitary-gonadal axis. Prepubertal Leydig cells, however, exhibit only very low-level RLF gene expression, this phenotype persisting in the adult hpg mouse. In summary, fetal Leydig cells express RLF in an LH/human CG-independent fashion, whereas LH/human CG is essential to induce RLF expression in the adult-type Leydig cell. In cultured adult Leydig cells or in the mouse tumor MA-10 cell line, RLF mRNA is expressed in a constitutive fashion. RLF thus seems to be a useful marker of Leydig cell differentiation status. |
doi_str_mv | 10.1210/endo.139.6.6046 |
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Expression of the relaxin-like factor (RLF) was studied at the messenger RNA (mRNA) and protein levels in the testes and ovaries of the mouse, as well as through testicular development and differentiation in the mouse testis. In situ hybridization or RT-PCR, and immunohistochemistry using a polyclonal antibody raised against a recombinant protein, provided mutually confirmatory results for a high expression of RLF in the Leydig cells of the adult testis and at a much lower level of expression in the luteal cells of the ovary through the cycle, pregnancy, and in lactation. Analysis of protein and mRNA expression, through postnatal testicular development, indicated moderate RLF expression also in the fetal population of Leydig cells, even in the hpg mutant mouse, lacking an active pituitary-gonadal axis. Prepubertal Leydig cells, however, exhibit only very low-level RLF gene expression, this phenotype persisting in the adult hpg mouse. In summary, fetal Leydig cells express RLF in an LH/human CG-independent fashion, whereas LH/human CG is essential to induce RLF expression in the adult-type Leydig cell. In cultured adult Leydig cells or in the mouse tumor MA-10 cell line, RLF mRNA is expressed in a constitutive fashion. RLF thus seems to be a useful marker of Leydig cell differentiation status.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/endo.139.6.6046</identifier><language>eng</language><publisher>Washington: Oxford University Press</publisher><subject>Biomarkers ; Cell differentiation ; Corpus luteum ; Differentiation (biology) ; Fetuses ; Gene expression ; Hybridization ; Immunohistochemistry ; Lactation ; Leydig cells ; Ovaries ; Phenotypes ; Pituitary ; Pituitary-gonadal axis ; Polyclonal antibodies ; Proteins ; Relaxin ; Relaxin-like factor ; Testes</subject><ispartof>Endocrinology (Philadelphia), 1998-06, Vol.139 (6), p.2960-2970</ispartof><rights>Copyright © 1998 by The Endocrine Society 1998</rights><rights>Copyright © 1998 by The Endocrine Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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></links><search><creatorcontrib>Balvers, M.</creatorcontrib><creatorcontrib>Spiess, A.-N.</creatorcontrib><creatorcontrib>Domagalski, R.</creatorcontrib><creatorcontrib>Hunt, N.</creatorcontrib><creatorcontrib>Kilic, E.</creatorcontrib><creatorcontrib>Mukhopadhyay, A. K.</creatorcontrib><creatorcontrib>Hanks, E.</creatorcontrib><creatorcontrib>Charlton, H. M.</creatorcontrib><creatorcontrib>Ivell, R.</creatorcontrib><title>Relaxin-Like Factor Expression as a Marker of Differentiation in the Mouse Testis and Ovary</title><title>Endocrinology (Philadelphia)</title><description>Abstract
Expression of the relaxin-like factor (RLF) was studied at the messenger RNA (mRNA) and protein levels in the testes and ovaries of the mouse, as well as through testicular development and differentiation in the mouse testis. In situ hybridization or RT-PCR, and immunohistochemistry using a polyclonal antibody raised against a recombinant protein, provided mutually confirmatory results for a high expression of RLF in the Leydig cells of the adult testis and at a much lower level of expression in the luteal cells of the ovary through the cycle, pregnancy, and in lactation. Analysis of protein and mRNA expression, through postnatal testicular development, indicated moderate RLF expression also in the fetal population of Leydig cells, even in the hpg mutant mouse, lacking an active pituitary-gonadal axis. Prepubertal Leydig cells, however, exhibit only very low-level RLF gene expression, this phenotype persisting in the adult hpg mouse. In summary, fetal Leydig cells express RLF in an LH/human CG-independent fashion, whereas LH/human CG is essential to induce RLF expression in the adult-type Leydig cell. In cultured adult Leydig cells or in the mouse tumor MA-10 cell line, RLF mRNA is expressed in a constitutive fashion. RLF thus seems to be a useful marker of Leydig cell differentiation status.</description><subject>Biomarkers</subject><subject>Cell differentiation</subject><subject>Corpus luteum</subject><subject>Differentiation (biology)</subject><subject>Fetuses</subject><subject>Gene expression</subject><subject>Hybridization</subject><subject>Immunohistochemistry</subject><subject>Lactation</subject><subject>Leydig cells</subject><subject>Ovaries</subject><subject>Phenotypes</subject><subject>Pituitary</subject><subject>Pituitary-gonadal axis</subject><subject>Polyclonal antibodies</subject><subject>Proteins</subject><subject>Relaxin</subject><subject>Relaxin-like factor</subject><subject>Testes</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNotkEFLAzEQhYMoWKtnrwFvwq6ZnWTTPUq1KrQUpJ48hLibxbQ1WZNdqf_eLPU0zLzHm8dHyDWwHApgd8Y1Pges8jIvGS9PyAQqLjIJkp2SCWOAmSwKeU4uYtymlXOOE_L-avb6YF22tDtDF7rufaCPhy6YGK13VEeq6UqHnQnUt_TBtq0JxvVW96NsHe0_DV35IRq6MbG3ye8auv7R4feSnLV6H83V_5ySt8XjZv6cLddPL_P7ZeYBoc-MEAYLOeNVhaIRvIC6qsWH1I1oZDppzkUrayEllhXMoGXAODLNC4MN1jOckptjbhf895BKqK0fgksvFQKylCuwSK7bo8sPneqC_UoNFTA1wlMjPJXgqVKN8PAPMVBg2g</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>Balvers, M.</creator><creator>Spiess, A.-N.</creator><creator>Domagalski, R.</creator><creator>Hunt, N.</creator><creator>Kilic, E.</creator><creator>Mukhopadhyay, A. K.</creator><creator>Hanks, E.</creator><creator>Charlton, H. M.</creator><creator>Ivell, R.</creator><general>Oxford University Press</general><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></search><sort><creationdate>19980601</creationdate><title>Relaxin-Like Factor Expression as a Marker of Differentiation in the Mouse Testis and Ovary</title><author>Balvers, M. ; Spiess, A.-N. ; Domagalski, R. ; Hunt, N. ; Kilic, E. ; Mukhopadhyay, A. K. ; Hanks, E. ; Charlton, H. M. ; Ivell, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-o131t-e55e327849935d5421c9c5b7ad5d7935a445f7c577369181f010430a42e3d3c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biomarkers</topic><topic>Cell differentiation</topic><topic>Corpus luteum</topic><topic>Differentiation (biology)</topic><topic>Fetuses</topic><topic>Gene expression</topic><topic>Hybridization</topic><topic>Immunohistochemistry</topic><topic>Lactation</topic><topic>Leydig cells</topic><topic>Ovaries</topic><topic>Phenotypes</topic><topic>Pituitary</topic><topic>Pituitary-gonadal axis</topic><topic>Polyclonal antibodies</topic><topic>Proteins</topic><topic>Relaxin</topic><topic>Relaxin-like factor</topic><topic>Testes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balvers, M.</creatorcontrib><creatorcontrib>Spiess, A.-N.</creatorcontrib><creatorcontrib>Domagalski, R.</creatorcontrib><creatorcontrib>Hunt, N.</creatorcontrib><creatorcontrib>Kilic, E.</creatorcontrib><creatorcontrib>Mukhopadhyay, A. K.</creatorcontrib><creatorcontrib>Hanks, E.</creatorcontrib><creatorcontrib>Charlton, H. M.</creatorcontrib><creatorcontrib>Ivell, R.</creatorcontrib><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><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balvers, M.</au><au>Spiess, A.-N.</au><au>Domagalski, R.</au><au>Hunt, N.</au><au>Kilic, E.</au><au>Mukhopadhyay, A. K.</au><au>Hanks, E.</au><au>Charlton, H. M.</au><au>Ivell, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relaxin-Like Factor Expression as a Marker of Differentiation in the Mouse Testis and Ovary</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><date>1998-06-01</date><risdate>1998</risdate><volume>139</volume><issue>6</issue><spage>2960</spage><epage>2970</epage><pages>2960-2970</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>Abstract
Expression of the relaxin-like factor (RLF) was studied at the messenger RNA (mRNA) and protein levels in the testes and ovaries of the mouse, as well as through testicular development and differentiation in the mouse testis. In situ hybridization or RT-PCR, and immunohistochemistry using a polyclonal antibody raised against a recombinant protein, provided mutually confirmatory results for a high expression of RLF in the Leydig cells of the adult testis and at a much lower level of expression in the luteal cells of the ovary through the cycle, pregnancy, and in lactation. Analysis of protein and mRNA expression, through postnatal testicular development, indicated moderate RLF expression also in the fetal population of Leydig cells, even in the hpg mutant mouse, lacking an active pituitary-gonadal axis. Prepubertal Leydig cells, however, exhibit only very low-level RLF gene expression, this phenotype persisting in the adult hpg mouse. In summary, fetal Leydig cells express RLF in an LH/human CG-independent fashion, whereas LH/human CG is essential to induce RLF expression in the adult-type Leydig cell. In cultured adult Leydig cells or in the mouse tumor MA-10 cell line, RLF mRNA is expressed in a constitutive fashion. RLF thus seems to be a useful marker of Leydig cell differentiation status.</abstract><cop>Washington</cop><pub>Oxford University Press</pub><doi>10.1210/endo.139.6.6046</doi><tpages>11</tpages></addata></record> |
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subjects | Biomarkers Cell differentiation Corpus luteum Differentiation (biology) Fetuses Gene expression Hybridization Immunohistochemistry Lactation Leydig cells Ovaries Phenotypes Pituitary Pituitary-gonadal axis Polyclonal antibodies Proteins Relaxin Relaxin-like factor Testes |
title | Relaxin-Like Factor Expression as a Marker of Differentiation in the Mouse Testis and Ovary |
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