Changes in expression and distribution of attractin in the testes of rats at different developmental stages
Attractin (Atrn), an autosomal recessive gene, is widely expressed in the body and displays multiple physiological and pathological functions in different types of tissues. The objective of this study was to localize Atrn protein and mRNA in the testis and epididymis of rats at different stages of m...
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Veröffentlicht in: | International journal of molecular medicine 2013-09, Vol.32 (3), p.599-606 |
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creator | SHANG, XUEJUN LIU, JUAN XU, QIUYU ZHANG, QI MA, BO WANG, YONGLU ZHANG, ZYUEHUA CAO, XIAOMEI ZHAN, XUXIN |
description | Attractin (Atrn), an autosomal recessive gene, is widely expressed in the body and displays multiple physiological and pathological functions in different types of tissues. The objective of this study was to localize Atrn protein and mRNA in the testis and epididymis of rats at different stages of maturation. Testis and epididymidis samples were obtained from the following 5 groups of Sprague Dawley (SD) rats in different developmental stages: newborn (8 h after birth), prepubertal (5 days), pubertal (20 days), postpubertal (50 days) and mature (70 days). Tissues were fixed and prepared for indirect immunofluorescence, immunohistochemistry, in situ hybridization, confocal laser scanning microscopy and western blot assays. A polyclonal antiserum against mouse Atrn and oligonucleotide riboprobes were used in the above assays. At the different stages of maturation, Atrn protein and mRNA were both widely expressed in the rat testis, including Leydig cells, primitive spermatogonia, primary spermatocytes, spermatids, Sertoli and peritubular myoid cells. Staining of the Atrn protein was mainly located on the cell membrane and in the cell cytoplasm while Atrn mRNA was distributed in both the nucleus and cytoplasm. No immunopositive staining was detected in spermatozoa and epididymides. In the epididymis, comprised of the caput, corpus and cauda, there was no definitive immunopositive staining within the efferent ductules or epididymal ducts. Taken together, Atrn protein and mRNA are both expressed widely in the rat testis at different stages of maturation, which suggests that Atrn protein is involved and plays an important role in the development of the reproductive system. In addition, the rat testis has the ability to synthesize Atrn protein throughout sexual development. |
doi_str_mv | 10.3892/ijmm.2013.1423 |
format | Article |
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The objective of this study was to localize Atrn protein and mRNA in the testis and epididymis of rats at different stages of maturation. Testis and epididymidis samples were obtained from the following 5 groups of Sprague Dawley (SD) rats in different developmental stages: newborn (8 h after birth), prepubertal (5 days), pubertal (20 days), postpubertal (50 days) and mature (70 days). Tissues were fixed and prepared for indirect immunofluorescence, immunohistochemistry, in situ hybridization, confocal laser scanning microscopy and western blot assays. A polyclonal antiserum against mouse Atrn and oligonucleotide riboprobes were used in the above assays. At the different stages of maturation, Atrn protein and mRNA were both widely expressed in the rat testis, including Leydig cells, primitive spermatogonia, primary spermatocytes, spermatids, Sertoli and peritubular myoid cells. Staining of the Atrn protein was mainly located on the cell membrane and in the cell cytoplasm while Atrn mRNA was distributed in both the nucleus and cytoplasm. No immunopositive staining was detected in spermatozoa and epididymides. In the epididymis, comprised of the caput, corpus and cauda, there was no definitive immunopositive staining within the efferent ductules or epididymal ducts. Taken together, Atrn protein and mRNA are both expressed widely in the rat testis at different stages of maturation, which suggests that Atrn protein is involved and plays an important role in the development of the reproductive system. In addition, the rat testis has the ability to synthesize Atrn protein throughout sexual development.</description><identifier>ISSN: 1107-3756</identifier><identifier>EISSN: 1791-244X</identifier><identifier>DOI: 10.3892/ijmm.2013.1423</identifier><identifier>PMID: 23799577</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>Age ; Animals ; Atrn mRNA ; Atrn protein ; epididymis ; Gene Expression Regulation, Developmental ; Immunohistochemistry ; In Situ Hybridization ; Laboratory animals ; Leydig Cells - metabolism ; Localization ; Male ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mutation ; Nervous system ; Organ Specificity - genetics ; Physiology ; Proteins ; Puberty ; Rats ; Reproductive system ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Rodents ; Sertoli Cells - metabolism ; stages of development ; Stem cells ; Sucrose ; testis ; Testis - embryology ; Testis - metabolism</subject><ispartof>International journal of molecular medicine, 2013-09, Vol.32 (3), p.599-606</ispartof><rights>Copyright © 2013, Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-c14fb2cc6ecfb3fd29a1958289cd176a71b4e845bcc9d131461993f4dab243023</citedby><cites>FETCH-LOGICAL-c396t-c14fb2cc6ecfb3fd29a1958289cd176a71b4e845bcc9d131461993f4dab243023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,5571,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23799577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SHANG, XUEJUN</creatorcontrib><creatorcontrib>LIU, JUAN</creatorcontrib><creatorcontrib>XU, QIUYU</creatorcontrib><creatorcontrib>ZHANG, QI</creatorcontrib><creatorcontrib>MA, BO</creatorcontrib><creatorcontrib>WANG, YONGLU</creatorcontrib><creatorcontrib>ZHANG, ZYUEHUA</creatorcontrib><creatorcontrib>CAO, XIAOMEI</creatorcontrib><creatorcontrib>ZHAN, XUXIN</creatorcontrib><title>Changes in expression and distribution of attractin in the testes of rats at different developmental stages</title><title>International journal of molecular medicine</title><addtitle>Int J Mol Med</addtitle><description>Attractin (Atrn), an autosomal recessive gene, is widely expressed in the body and displays multiple physiological and pathological functions in different types of tissues. The objective of this study was to localize Atrn protein and mRNA in the testis and epididymis of rats at different stages of maturation. Testis and epididymidis samples were obtained from the following 5 groups of Sprague Dawley (SD) rats in different developmental stages: newborn (8 h after birth), prepubertal (5 days), pubertal (20 days), postpubertal (50 days) and mature (70 days). Tissues were fixed and prepared for indirect immunofluorescence, immunohistochemistry, in situ hybridization, confocal laser scanning microscopy and western blot assays. A polyclonal antiserum against mouse Atrn and oligonucleotide riboprobes were used in the above assays. At the different stages of maturation, Atrn protein and mRNA were both widely expressed in the rat testis, including Leydig cells, primitive spermatogonia, primary spermatocytes, spermatids, Sertoli and peritubular myoid cells. Staining of the Atrn protein was mainly located on the cell membrane and in the cell cytoplasm while Atrn mRNA was distributed in both the nucleus and cytoplasm. No immunopositive staining was detected in spermatozoa and epididymides. In the epididymis, comprised of the caput, corpus and cauda, there was no definitive immunopositive staining within the efferent ductules or epididymal ducts. Taken together, Atrn protein and mRNA are both expressed widely in the rat testis at different stages of maturation, which suggests that Atrn protein is involved and plays an important role in the development of the reproductive system. In addition, the rat testis has the ability to synthesize Atrn protein throughout sexual development.</description><subject>Age</subject><subject>Animals</subject><subject>Atrn mRNA</subject><subject>Atrn protein</subject><subject>epididymis</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Laboratory animals</subject><subject>Leydig Cells - metabolism</subject><subject>Localization</subject><subject>Male</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mutation</subject><subject>Nervous system</subject><subject>Organ Specificity - genetics</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Puberty</subject><subject>Rats</subject><subject>Reproductive system</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Sertoli Cells - metabolism</subject><subject>stages of development</subject><subject>Stem cells</subject><subject>Sucrose</subject><subject>testis</subject><subject>Testis - embryology</subject><subject>Testis - metabolism</subject><issn>1107-3756</issn><issn>1791-244X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kMtLxDAQxoMo7rp69SgFL15SM3m0zVEWX7DgRcFbSdPE7bp9mKSi_70puy4M5CPzm2-GD6FLICkrJL1tNm2bUgIsBU7ZEZpDLgFTzt-PowaSY5aLbIbOvN8QQgWXxSmaUZZLKfJ8jj6Xa9V9GJ80XWJ-Bme8b_ouUV2d1I0PrqnGMH30NlEhOKVDBGOFtUmC8bGmllPBx34csdY400Vlvs22H9qo1TbxQcUd5-jEqq03F_t3gd4e7l-XT3j18vi8vFthzWQWsAZuK6p1ZrStmK2pVCBFQQupa8gzlUPFTcFFpbWsgQHPQEpmea0qyhmhbIGud76D67_GeGS56UfXxZUlSEaZAAIiUumO0q733hlbDq5plfstgZRTtuWUbTllW07ZxoGrve1YtaY-4P9hRuBmB_gh5tfUvT8wkxVmFBOGiYjX_gHzD4Rr</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>SHANG, XUEJUN</creator><creator>LIU, JUAN</creator><creator>XU, QIUYU</creator><creator>ZHANG, QI</creator><creator>MA, BO</creator><creator>WANG, YONGLU</creator><creator>ZHANG, ZYUEHUA</creator><creator>CAO, XIAOMEI</creator><creator>ZHAN, XUXIN</creator><general>D.A. Spandidos</general><general>Spandidos Publications UK Ltd</general><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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20130901</creationdate><title>Changes in expression and distribution of attractin in the testes of rats at different developmental stages</title><author>SHANG, XUEJUN ; LIU, JUAN ; XU, QIUYU ; ZHANG, QI ; MA, BO ; WANG, YONGLU ; ZHANG, ZYUEHUA ; CAO, XIAOMEI ; ZHAN, XUXIN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-c14fb2cc6ecfb3fd29a1958289cd176a71b4e845bcc9d131461993f4dab243023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Age</topic><topic>Animals</topic><topic>Atrn mRNA</topic><topic>Atrn protein</topic><topic>epididymis</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Laboratory animals</topic><topic>Leydig Cells - metabolism</topic><topic>Localization</topic><topic>Male</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Mutation</topic><topic>Nervous system</topic><topic>Organ Specificity - genetics</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Puberty</topic><topic>Rats</topic><topic>Reproductive system</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Rodents</topic><topic>Sertoli Cells - metabolism</topic><topic>stages of development</topic><topic>Stem cells</topic><topic>Sucrose</topic><topic>testis</topic><topic>Testis - embryology</topic><topic>Testis - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHANG, XUEJUN</creatorcontrib><creatorcontrib>LIU, JUAN</creatorcontrib><creatorcontrib>XU, QIUYU</creatorcontrib><creatorcontrib>ZHANG, QI</creatorcontrib><creatorcontrib>MA, BO</creatorcontrib><creatorcontrib>WANG, YONGLU</creatorcontrib><creatorcontrib>ZHANG, ZYUEHUA</creatorcontrib><creatorcontrib>CAO, XIAOMEI</creatorcontrib><creatorcontrib>ZHAN, XUXIN</creatorcontrib><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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><jtitle>International journal of molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SHANG, XUEJUN</au><au>LIU, JUAN</au><au>XU, QIUYU</au><au>ZHANG, QI</au><au>MA, BO</au><au>WANG, YONGLU</au><au>ZHANG, ZYUEHUA</au><au>CAO, XIAOMEI</au><au>ZHAN, XUXIN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in expression and distribution of attractin in the testes of rats at different developmental stages</atitle><jtitle>International journal of molecular medicine</jtitle><addtitle>Int J Mol Med</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>32</volume><issue>3</issue><spage>599</spage><epage>606</epage><pages>599-606</pages><issn>1107-3756</issn><eissn>1791-244X</eissn><abstract>Attractin (Atrn), an autosomal recessive gene, is widely expressed in the body and displays multiple physiological and pathological functions in different types of tissues. The objective of this study was to localize Atrn protein and mRNA in the testis and epididymis of rats at different stages of maturation. Testis and epididymidis samples were obtained from the following 5 groups of Sprague Dawley (SD) rats in different developmental stages: newborn (8 h after birth), prepubertal (5 days), pubertal (20 days), postpubertal (50 days) and mature (70 days). Tissues were fixed and prepared for indirect immunofluorescence, immunohistochemistry, in situ hybridization, confocal laser scanning microscopy and western blot assays. A polyclonal antiserum against mouse Atrn and oligonucleotide riboprobes were used in the above assays. At the different stages of maturation, Atrn protein and mRNA were both widely expressed in the rat testis, including Leydig cells, primitive spermatogonia, primary spermatocytes, spermatids, Sertoli and peritubular myoid cells. Staining of the Atrn protein was mainly located on the cell membrane and in the cell cytoplasm while Atrn mRNA was distributed in both the nucleus and cytoplasm. No immunopositive staining was detected in spermatozoa and epididymides. In the epididymis, comprised of the caput, corpus and cauda, there was no definitive immunopositive staining within the efferent ductules or epididymal ducts. Taken together, Atrn protein and mRNA are both expressed widely in the rat testis at different stages of maturation, which suggests that Atrn protein is involved and plays an important role in the development of the reproductive system. In addition, the rat testis has the ability to synthesize Atrn protein throughout sexual development.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>23799577</pmid><doi>10.3892/ijmm.2013.1423</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Animals Atrn mRNA Atrn protein epididymis Gene Expression Regulation, Developmental Immunohistochemistry In Situ Hybridization Laboratory animals Leydig Cells - metabolism Localization Male Membrane Proteins - genetics Membrane Proteins - metabolism Mutation Nervous system Organ Specificity - genetics Physiology Proteins Puberty Rats Reproductive system RNA, Messenger - genetics RNA, Messenger - metabolism Rodents Sertoli Cells - metabolism stages of development Stem cells Sucrose testis Testis - embryology Testis - metabolism |
title | Changes in expression and distribution of attractin in the testes of rats at different developmental stages |
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