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
Hauptverfasser: ROSCOE, Wendi A, BARR, Kevin J, MHAWI, Abdul Amir, POMERANTZ, David K, KIDDER, Gerald M
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container_issue 3
container_start_page 829
container_title Biology of reproduction
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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 “Sertoli cell only” phenotype. These results indicate that intercellular communication via Cx43 channels is required for postnatal expansion of the male germ line.
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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. 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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. 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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 “Sertoli cell only” 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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