A BKCa to Kv Switch During Spermatogenesis in the Rat Seminiferous Tubules
Spermatogenesis is a complex cellular event during which the diploid germ cells differentiate and divide by mitosis and meiosis at specific time points along the spermatogenic cycle to generate the haploid spermatozoa. For this complex event to go in an orderly manner, cell differentiation and divis...
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Veröffentlicht in: | Biology of reproduction 2002-07, Vol.67 (1), p.46-54 |
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creator | GONG, X. D LI, J. C. H LEUNG, G. P. H CHEUNG, K. H WONG, P. Y. D |
description | Spermatogenesis is a complex cellular event during which the diploid germ cells differentiate and divide by mitosis and meiosis
at specific time points along the spermatogenic cycle to generate the haploid spermatozoa. For this complex event to go in
an orderly manner, cell differentiation and division must be precisely controlled by signals arising from within and outside
the seminiferous tubules. Changes in the membrane potential of the germ cells are likely to be an important part of the signaling
mechanism. We have applied the whole-cell patch clamp technique to identify and characterize ion channels in different spermatogenic
cells from immature and mature rat testes fractionated by discontinuous Percoll gradient. A voltage- and Ca 2+ - dependent, outwardly rectifying current with gating and pharmacologic properties resembling the large conductance K + channels (BK Ca ) was recorded from the spermatogonia and primary spermatocytes. Another voltage-dependent, outwardly rectifying current that
was sensitive to 4-aminopyridine, a K v channel blocker, was detected in spermatocytes and early spermatids. This current is likely caused by the smaller conductance,
voltage-sensitive K + channels (K v ). In some spermatogonia, both the BK Ca channels and the K v channels could be simultaneously detected in the same cell. It appears that during the course of spermatogenesis, there is
up-regulation of K v but down-regulation of BK Ca . Reverse transcription-polymerase chain reaction, Western blot analysis, and immunohistochemistry further confirmed the differential
expression of the ion channels in different spermatogenic cells. We conclude that these ion channels may play an important
role in the control of spermatogenesis. |
doi_str_mv | 10.1095/biolreprod67.1.46 |
format | Article |
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at specific time points along the spermatogenic cycle to generate the haploid spermatozoa. For this complex event to go in
an orderly manner, cell differentiation and division must be precisely controlled by signals arising from within and outside
the seminiferous tubules. Changes in the membrane potential of the germ cells are likely to be an important part of the signaling
mechanism. We have applied the whole-cell patch clamp technique to identify and characterize ion channels in different spermatogenic
cells from immature and mature rat testes fractionated by discontinuous Percoll gradient. A voltage- and Ca 2+ - dependent, outwardly rectifying current with gating and pharmacologic properties resembling the large conductance K + channels (BK Ca ) was recorded from the spermatogonia and primary spermatocytes. Another voltage-dependent, outwardly rectifying current that
was sensitive to 4-aminopyridine, a K v channel blocker, was detected in spermatocytes and early spermatids. This current is likely caused by the smaller conductance,
voltage-sensitive K + channels (K v ). In some spermatogonia, both the BK Ca channels and the K v channels could be simultaneously detected in the same cell. It appears that during the course of spermatogenesis, there is
up-regulation of K v but down-regulation of BK Ca . Reverse transcription-polymerase chain reaction, Western blot analysis, and immunohistochemistry further confirmed the differential
expression of the ion channels in different spermatogenic cells. We conclude that these ion channels may play an important
role in the control of spermatogenesis.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod67.1.46</identifier><identifier>PMID: 12079998</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Mammalian male genital system ; Morphology. Physiology ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 2002-07, Vol.67 (1), p.46-54</ispartof><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13757588$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>GONG, X. D</creatorcontrib><creatorcontrib>LI, J. C. H</creatorcontrib><creatorcontrib>LEUNG, G. P. H</creatorcontrib><creatorcontrib>CHEUNG, K. H</creatorcontrib><creatorcontrib>WONG, P. Y. D</creatorcontrib><title>A BKCa to Kv Switch During Spermatogenesis in the Rat Seminiferous Tubules</title><title>Biology of reproduction</title><description>Spermatogenesis is a complex cellular event during which the diploid germ cells differentiate and divide by mitosis and meiosis
at specific time points along the spermatogenic cycle to generate the haploid spermatozoa. For this complex event to go in
an orderly manner, cell differentiation and division must be precisely controlled by signals arising from within and outside
the seminiferous tubules. Changes in the membrane potential of the germ cells are likely to be an important part of the signaling
mechanism. We have applied the whole-cell patch clamp technique to identify and characterize ion channels in different spermatogenic
cells from immature and mature rat testes fractionated by discontinuous Percoll gradient. A voltage- and Ca 2+ - dependent, outwardly rectifying current with gating and pharmacologic properties resembling the large conductance K + channels (BK Ca ) was recorded from the spermatogonia and primary spermatocytes. Another voltage-dependent, outwardly rectifying current that
was sensitive to 4-aminopyridine, a K v channel blocker, was detected in spermatocytes and early spermatids. This current is likely caused by the smaller conductance,
voltage-sensitive K + channels (K v ). In some spermatogonia, both the BK Ca channels and the K v channels could be simultaneously detected in the same cell. It appears that during the course of spermatogenesis, there is
up-regulation of K v but down-regulation of BK Ca . Reverse transcription-polymerase chain reaction, Western blot analysis, and immunohistochemistry further confirmed the differential
expression of the ion channels in different spermatogenic cells. We conclude that these ion channels may play an important
role in the control of spermatogenesis.</description><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Mammalian male genital system</subject><subject>Morphology. Physiology</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNotzE1PwyAcgHFiNG5OP4A3DnrsBP6FwnHO9y0xcfPcUAorpm-B1sZvr0ZPz-WXB6FLSpaUKH5T-K4Otg9dKbIlXabiCM0pZyrJmJDHaE4IEQmAgBk6i_GDEJoCg1M0o4xkSik5Ry8rfLtZazx0ePOJd5MfTIXvxuDbA971NjR66A62tdFH7Fs8VBa_6QHvbONb72zoxoj3YzHWNp6jE6fraC_-u0DvD_f79VOyfX18Xq-2SUVZNiQ2NZRw5RQA04V0nDleloIpp7VNWSopVaUApYUwJZgCOP_RwCQFyamRsEDXf99eR6NrF3RrfMz74BsdvnIKGc-4_HVXf67yh2ryweax0XXdjwXk0zSJLKd5KuAbFBZfIQ</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>GONG, X. D</creator><creator>LI, J. C. H</creator><creator>LEUNG, G. P. H</creator><creator>CHEUNG, K. H</creator><creator>WONG, P. Y. D</creator><general>Society for the Study of Reproduction</general><scope>IQODW</scope></search><sort><creationdate>20020701</creationdate><title>A BKCa to Kv Switch During Spermatogenesis in the Rat Seminiferous Tubules</title><author>GONG, X. D ; LI, J. C. H ; LEUNG, G. P. H ; CHEUNG, K. H ; WONG, P. Y. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h127t-e4c1059f9332ab8f52f5dd629faae4248119d639a66cd3cb35559f32813851c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Mammalian male genital system</topic><topic>Morphology. Physiology</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GONG, X. D</creatorcontrib><creatorcontrib>LI, J. C. H</creatorcontrib><creatorcontrib>LEUNG, G. P. H</creatorcontrib><creatorcontrib>CHEUNG, K. H</creatorcontrib><creatorcontrib>WONG, P. Y. D</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GONG, X. D</au><au>LI, J. C. H</au><au>LEUNG, G. P. H</au><au>CHEUNG, K. H</au><au>WONG, P. Y. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A BKCa to Kv Switch During Spermatogenesis in the Rat Seminiferous Tubules</atitle><jtitle>Biology of reproduction</jtitle><date>2002-07-01</date><risdate>2002</risdate><volume>67</volume><issue>1</issue><spage>46</spage><epage>54</epage><pages>46-54</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>Spermatogenesis is a complex cellular event during which the diploid germ cells differentiate and divide by mitosis and meiosis
at specific time points along the spermatogenic cycle to generate the haploid spermatozoa. For this complex event to go in
an orderly manner, cell differentiation and division must be precisely controlled by signals arising from within and outside
the seminiferous tubules. Changes in the membrane potential of the germ cells are likely to be an important part of the signaling
mechanism. We have applied the whole-cell patch clamp technique to identify and characterize ion channels in different spermatogenic
cells from immature and mature rat testes fractionated by discontinuous Percoll gradient. A voltage- and Ca 2+ - dependent, outwardly rectifying current with gating and pharmacologic properties resembling the large conductance K + channels (BK Ca ) was recorded from the spermatogonia and primary spermatocytes. Another voltage-dependent, outwardly rectifying current that
was sensitive to 4-aminopyridine, a K v channel blocker, was detected in spermatocytes and early spermatids. This current is likely caused by the smaller conductance,
voltage-sensitive K + channels (K v ). In some spermatogonia, both the BK Ca channels and the K v channels could be simultaneously detected in the same cell. It appears that during the course of spermatogenesis, there is
up-regulation of K v but down-regulation of BK Ca . Reverse transcription-polymerase chain reaction, Western blot analysis, and immunohistochemistry further confirmed the differential
expression of the ion channels in different spermatogenic cells. We conclude that these ion channels may play an important
role in the control of spermatogenesis.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>12079998</pmid><doi>10.1095/biolreprod67.1.46</doi><tpages>9</tpages></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; BioOne Complete; Oxford University Press Journals All Titles (1996-Current) |
subjects | Biological and medical sciences Fundamental and applied biological sciences. Psychology Mammalian male genital system Morphology. Physiology Vertebrates: reproduction |
title | A BKCa to Kv Switch During Spermatogenesis in the Rat Seminiferous Tubules |
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