Failure of Spermatogenesis in Mice Lacking Connexin43
Connexin43 (Cx43), a gap junction protein encoded by the Gja1 gene, is expressed in several cell types of the testis. Cx43 gap junctions couple Sertoli cells with each other, Leydig cells with each other, and spermatogonia/spermatocytes with Sertoli cells. To investigate the role of this communicati...
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Veröffentlicht in: | Biology of reproduction 2001-09, Vol.65 (3), p.829-838 |
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creator | ROSCOE, Wendi A BARR, Kevin J MHAWI, Abdul Amir POMERANTZ, David K KIDDER, Gerald M |
description | Connexin43 (Cx43), a gap junction protein encoded by the Gja1 gene, is expressed in several cell types of the testis. Cx43 gap junctions couple Sertoli cells with each other, Leydig cells
with each other, and spermatogonia/spermatocytes with Sertoli cells. To investigate the role of this communication pathway
in spermatogenesis, we studied postnatal testis development in mice lacking Cx43. Because such mice die shortly after birth,
it was necessary to graft testes from null mutant fetuses under the kidney capsules of adult males for up to 3 wk. Grafted
wild-type testes were used as controls. In our initial experiments with wild-type testes, histological examination indicated
that the development of grafted testes kept pace with that of nongrafted testes in terms of the onset of meiosis, but this
development required the presence of the host gonads. When excised grafts were stimulated in vitro with cAMP or LH, there
was no significant difference in androgen production between null mutant and wild-type testes, indicating that the absence
of Cx43 had not compromised steroidogenesis. Previous research has shown that Cx43 null mutant neonates have a germ cell deficiency
that arises during fetal life, and our analysis of grafted testes demonstrated that this deficiency persists postnatally,
giving rise to a âSertoli cell onlyâ phenotype. These results indicate that intercellular communication via Cx43 channels
is required for postnatal expansion of the male germ line. |
doi_str_mv | 10.1095/biolreprod65.3.829 |
format | Article |
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with each other, and spermatogonia/spermatocytes with Sertoli cells. To investigate the role of this communication pathway
in spermatogenesis, we studied postnatal testis development in mice lacking Cx43. Because such mice die shortly after birth,
it was necessary to graft testes from null mutant fetuses under the kidney capsules of adult males for up to 3 wk. Grafted
wild-type testes were used as controls. In our initial experiments with wild-type testes, histological examination indicated
that the development of grafted testes kept pace with that of nongrafted testes in terms of the onset of meiosis, but this
development required the presence of the host gonads. When excised grafts were stimulated in vitro with cAMP or LH, there
was no significant difference in androgen production between null mutant and wild-type testes, indicating that the absence
of Cx43 had not compromised steroidogenesis. Previous research has shown that Cx43 null mutant neonates have a germ cell deficiency
that arises during fetal life, and our analysis of grafted testes demonstrated that this deficiency persists postnatally,
giving rise to a âSertoli cell onlyâ phenotype. These results indicate that intercellular communication via Cx43 channels
is required for postnatal expansion of the male germ line.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod65.3.829</identifier><identifier>PMID: 11514348</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Animals ; Apoptosis ; Biological and medical sciences ; Cell Division ; Connexin 43 - deficiency ; Connexin 43 - genetics ; Connexin 43 - physiology ; Cyclic AMP - pharmacology ; Fundamental and applied biological sciences. Psychology ; Genotype ; Immunohistochemistry ; In Situ Nick-End Labeling ; Kidney ; Leydig Cells - ultrastructure ; Luteinizing Hormone - pharmacology ; Male ; Mammalian male genital system ; Meiosis ; Mice ; Mice, Knockout ; Microscopy, Electron ; Morphology. Physiology ; Mutation ; Oligospermia - genetics ; Oligospermia - pathology ; Oligospermia - physiopathology ; Proliferating Cell Nuclear Antigen - analysis ; Seminiferous Tubules - pathology ; Spermatogenesis - physiology ; Testis - embryology ; Testis - physiopathology ; Testis - transplantation ; Testosterone - biosynthesis ; Transplantation, Heterotopic ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 2001-09, Vol.65 (3), p.829-838</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14129817$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11514348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ROSCOE, Wendi A</creatorcontrib><creatorcontrib>BARR, Kevin J</creatorcontrib><creatorcontrib>MHAWI, Abdul Amir</creatorcontrib><creatorcontrib>POMERANTZ, David K</creatorcontrib><creatorcontrib>KIDDER, Gerald M</creatorcontrib><title>Failure of Spermatogenesis in Mice Lacking Connexin43</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>Connexin43 (Cx43), a gap junction protein encoded by the Gja1 gene, is expressed in several cell types of the testis. Cx43 gap junctions couple Sertoli cells with each other, Leydig cells
with each other, and spermatogonia/spermatocytes with Sertoli cells. To investigate the role of this communication pathway
in spermatogenesis, we studied postnatal testis development in mice lacking Cx43. Because such mice die shortly after birth,
it was necessary to graft testes from null mutant fetuses under the kidney capsules of adult males for up to 3 wk. Grafted
wild-type testes were used as controls. In our initial experiments with wild-type testes, histological examination indicated
that the development of grafted testes kept pace with that of nongrafted testes in terms of the onset of meiosis, but this
development required the presence of the host gonads. When excised grafts were stimulated in vitro with cAMP or LH, there
was no significant difference in androgen production between null mutant and wild-type testes, indicating that the absence
of Cx43 had not compromised steroidogenesis. Previous research has shown that Cx43 null mutant neonates have a germ cell deficiency
that arises during fetal life, and our analysis of grafted testes demonstrated that this deficiency persists postnatally,
giving rise to a âSertoli cell onlyâ phenotype. These results indicate that intercellular communication via Cx43 channels
is required for postnatal expansion of the male germ line.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Connexin 43 - deficiency</subject><subject>Connexin 43 - genetics</subject><subject>Connexin 43 - physiology</subject><subject>Cyclic AMP - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genotype</subject><subject>Immunohistochemistry</subject><subject>In Situ Nick-End Labeling</subject><subject>Kidney</subject><subject>Leydig Cells - ultrastructure</subject><subject>Luteinizing Hormone - pharmacology</subject><subject>Male</subject><subject>Mammalian male genital system</subject><subject>Meiosis</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Microscopy, Electron</subject><subject>Morphology. Physiology</subject><subject>Mutation</subject><subject>Oligospermia - genetics</subject><subject>Oligospermia - pathology</subject><subject>Oligospermia - physiopathology</subject><subject>Proliferating Cell Nuclear Antigen - analysis</subject><subject>Seminiferous Tubules - pathology</subject><subject>Spermatogenesis - physiology</subject><subject>Testis - embryology</subject><subject>Testis - physiopathology</subject><subject>Testis - transplantation</subject><subject>Testosterone - biosynthesis</subject><subject>Transplantation, Heterotopic</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0D1PwzAQBmALgWgp_AEGlAW2FH_EHxlRRQGpiAGYLce5tIbEKXajwL_HEkWd7oZHr-49hC4JnhNc8tvK9W2Abehrwedsrmh5hKaE0zKXVKhjNMUYi5wxwSboLMYPjEnBKDtFE0J4Wgs1RXxpXDsEyPome91C6MyuX4OH6GLmfPbsLGQrYz-dX2eL3nv4dr5g5-ikMW2Ei_2coffl_dviMV-9PDwt7lb5hgq5y6t0jLK1KoysysZKZayQQlpBGSONkLLmtaBYEWtL4IkUBKAkDYbGYGCSzdDNX24q-TVA3OnORQttazz0Q9SSkEJxghO82sOh6qDW2-A6E370f9EErvfARGvaJhhvXTy4gtBSEXlwG7fejC6Ajp1p2xTL9DiOgmum06PZL4jdb-4</recordid><startdate>20010901</startdate><enddate>20010901</enddate><creator>ROSCOE, Wendi A</creator><creator>BARR, Kevin J</creator><creator>MHAWI, Abdul Amir</creator><creator>POMERANTZ, David K</creator><creator>KIDDER, Gerald M</creator><general>Society for the Study of Reproduction</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20010901</creationdate><title>Failure of Spermatogenesis in Mice Lacking Connexin43</title><author>ROSCOE, Wendi A ; BARR, Kevin J ; MHAWI, Abdul Amir ; POMERANTZ, David K ; KIDDER, Gerald M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h267t-b1528cd84a7b9fc78ac6767c62331f677d5d62081cc9e5b9f41ee91f0efa0e373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cell Division</topic><topic>Connexin 43 - deficiency</topic><topic>Connexin 43 - genetics</topic><topic>Connexin 43 - physiology</topic><topic>Cyclic AMP - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genotype</topic><topic>Immunohistochemistry</topic><topic>In Situ Nick-End Labeling</topic><topic>Kidney</topic><topic>Leydig Cells - ultrastructure</topic><topic>Luteinizing Hormone - pharmacology</topic><topic>Male</topic><topic>Mammalian male genital system</topic><topic>Meiosis</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Microscopy, Electron</topic><topic>Morphology. Physiology</topic><topic>Mutation</topic><topic>Oligospermia - genetics</topic><topic>Oligospermia - pathology</topic><topic>Oligospermia - physiopathology</topic><topic>Proliferating Cell Nuclear Antigen - analysis</topic><topic>Seminiferous Tubules - pathology</topic><topic>Spermatogenesis - physiology</topic><topic>Testis - embryology</topic><topic>Testis - physiopathology</topic><topic>Testis - transplantation</topic><topic>Testosterone - biosynthesis</topic><topic>Transplantation, Heterotopic</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ROSCOE, Wendi A</creatorcontrib><creatorcontrib>BARR, Kevin J</creatorcontrib><creatorcontrib>MHAWI, Abdul Amir</creatorcontrib><creatorcontrib>POMERANTZ, David K</creatorcontrib><creatorcontrib>KIDDER, Gerald M</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>MEDLINE - Academic</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ROSCOE, Wendi A</au><au>BARR, Kevin J</au><au>MHAWI, Abdul Amir</au><au>POMERANTZ, David K</au><au>KIDDER, Gerald M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Failure of Spermatogenesis in Mice Lacking Connexin43</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2001-09-01</date><risdate>2001</risdate><volume>65</volume><issue>3</issue><spage>829</spage><epage>838</epage><pages>829-838</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>Connexin43 (Cx43), a gap junction protein encoded by the Gja1 gene, is expressed in several cell types of the testis. Cx43 gap junctions couple Sertoli cells with each other, Leydig cells
with each other, and spermatogonia/spermatocytes with Sertoli cells. To investigate the role of this communication pathway
in spermatogenesis, we studied postnatal testis development in mice lacking Cx43. Because such mice die shortly after birth,
it was necessary to graft testes from null mutant fetuses under the kidney capsules of adult males for up to 3 wk. Grafted
wild-type testes were used as controls. In our initial experiments with wild-type testes, histological examination indicated
that the development of grafted testes kept pace with that of nongrafted testes in terms of the onset of meiosis, but this
development required the presence of the host gonads. When excised grafts were stimulated in vitro with cAMP or LH, there
was no significant difference in androgen production between null mutant and wild-type testes, indicating that the absence
of Cx43 had not compromised steroidogenesis. Previous research has shown that Cx43 null mutant neonates have a germ cell deficiency
that arises during fetal life, and our analysis of grafted testes demonstrated that this deficiency persists postnatally,
giving rise to a âSertoli cell onlyâ phenotype. These results indicate that intercellular communication via Cx43 channels
is required for postnatal expansion of the male germ line.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>11514348</pmid><doi>10.1095/biolreprod65.3.829</doi><tpages>10</tpages></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; BioOne Complete |
subjects | Animals Apoptosis Biological and medical sciences Cell Division Connexin 43 - deficiency Connexin 43 - genetics Connexin 43 - physiology Cyclic AMP - pharmacology Fundamental and applied biological sciences. Psychology Genotype Immunohistochemistry In Situ Nick-End Labeling Kidney Leydig Cells - ultrastructure Luteinizing Hormone - pharmacology Male Mammalian male genital system Meiosis Mice Mice, Knockout Microscopy, Electron Morphology. Physiology Mutation Oligospermia - genetics Oligospermia - pathology Oligospermia - physiopathology Proliferating Cell Nuclear Antigen - analysis Seminiferous Tubules - pathology Spermatogenesis - physiology Testis - embryology Testis - physiopathology Testis - transplantation Testosterone - biosynthesis Transplantation, Heterotopic Vertebrates: reproduction |
title | Failure of Spermatogenesis in Mice Lacking Connexin43 |
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