去甲肾上腺素通过连接蛋白43间隙连接泛素化抑制大鼠心肌细胞间偶联。

Q2 Biochemistry, Genetics and Molecular Biology
Cell Communication and Adhesion Pub Date : 2011-08-01 Epub Date: 2011-09-21 DOI:10.3109/15419061.2011.611920
Sarah Mollerup, Johannes P Hofgaard, Thomas H Braunstein, Ane Kjenseth, Edward Leithe, Edgar Rivedal, Niels-Henrik Holstein-Rathlou, Morten Schak Nielsen
{"title":"去甲肾上腺素通过连接蛋白43间隙连接泛素化抑制大鼠心肌细胞间偶联。","authors":"Sarah Mollerup,&nbsp;Johannes P Hofgaard,&nbsp;Thomas H Braunstein,&nbsp;Ane Kjenseth,&nbsp;Edward Leithe,&nbsp;Edgar Rivedal,&nbsp;Niels-Henrik Holstein-Rathlou,&nbsp;Morten Schak Nielsen","doi":"10.3109/15419061.2011.611920","DOIUrl":null,"url":null,"abstract":"<p><strong>Unlabelled: </strong>Gαq-stimulation reduces intercellular coupling within 10 min via a decrease in the membrane lipid phosphatidylinositol-4,5-bisphosphate (PIP2), but the mechanism is unknown. Here we show that uncoupling in rat cardiomyocytes after stimulation of α-adrenergic Gαq-coupled receptors with norepinephrine is prevented by proteasomal and lysosomal inhibitors, suggesting that internalization and possibly degradation of connexin43 (Cx43) is involved. Uncoupling was accompanied by increased Triton X-100 solubility of Cx43, which is considered a measure of the non-junctional pool of Cx43. However, inhibition of the proteasome and lysosome further increased solubility while preserving coupling, suggesting that communicating gap junctions can be part of the soluble fraction. Ubiquitination of Cx43 was also increased, and Cx43 co-immunoprecipitated with the ubiquitin ligase Nedd4.</p><p><strong>Conclusions: </strong>Norepinephrine increases ubiquitination of Cx43 in cardiomyocytes, possibly via Nedd4. We suggest that Cx43 is subsequently internalized, which is preceded by acquired solubility in Triton X-100, which does not lead to uncoupling per se.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"18 4","pages":"57-65"},"PeriodicalIF":0.0000,"publicationDate":"2011-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2011.611920","citationCount":"21","resultStr":"{\"title\":\"Norepinephrine inhibits intercellular coupling in rat cardiomyocytes by ubiquitination of connexin43 gap junctions.\",\"authors\":\"Sarah Mollerup,&nbsp;Johannes P Hofgaard,&nbsp;Thomas H Braunstein,&nbsp;Ane Kjenseth,&nbsp;Edward Leithe,&nbsp;Edgar Rivedal,&nbsp;Niels-Henrik Holstein-Rathlou,&nbsp;Morten Schak Nielsen\",\"doi\":\"10.3109/15419061.2011.611920\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Unlabelled: </strong>Gαq-stimulation reduces intercellular coupling within 10 min via a decrease in the membrane lipid phosphatidylinositol-4,5-bisphosphate (PIP2), but the mechanism is unknown. Here we show that uncoupling in rat cardiomyocytes after stimulation of α-adrenergic Gαq-coupled receptors with norepinephrine is prevented by proteasomal and lysosomal inhibitors, suggesting that internalization and possibly degradation of connexin43 (Cx43) is involved. Uncoupling was accompanied by increased Triton X-100 solubility of Cx43, which is considered a measure of the non-junctional pool of Cx43. However, inhibition of the proteasome and lysosome further increased solubility while preserving coupling, suggesting that communicating gap junctions can be part of the soluble fraction. Ubiquitination of Cx43 was also increased, and Cx43 co-immunoprecipitated with the ubiquitin ligase Nedd4.</p><p><strong>Conclusions: </strong>Norepinephrine increases ubiquitination of Cx43 in cardiomyocytes, possibly via Nedd4. We suggest that Cx43 is subsequently internalized, which is preceded by acquired solubility in Triton X-100, which does not lead to uncoupling per se.</p>\",\"PeriodicalId\":55269,\"journal\":{\"name\":\"Cell Communication and Adhesion\",\"volume\":\"18 4\",\"pages\":\"57-65\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.3109/15419061.2011.611920\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Communication and Adhesion\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3109/15419061.2011.611920\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2011/9/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Communication and Adhesion","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/15419061.2011.611920","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2011/9/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 21

摘要

未标记:g αq刺激通过降低膜脂磷脂酰肌醇-4,5-二磷酸(PIP2)在10分钟内减少细胞间偶联,但其机制尚不清楚。本研究表明,在用去甲肾上腺素刺激α-肾上腺素能g - αq偶联受体后,大鼠心肌细胞的解偶联可被蛋白酶体和溶酶体抑制剂阻止,这表明连接蛋白43 (Cx43)的内化和可能的降解参与其中。解耦伴随着Cx43的Triton X-100溶解度的增加,这被认为是Cx43非连接池的测量。然而,蛋白酶体和溶酶体的抑制在保持偶联的同时进一步增加了溶解度,这表明通信间隙连接可能是可溶性部分的一部分。Cx43的泛素化也增加,并且Cx43与泛素连接酶Nedd4共免疫沉淀。结论:去甲肾上腺素可能通过Nedd4增加心肌细胞中Cx43的泛素化。我们认为Cx43随后被内化,这之前在Triton X-100中获得溶解度,这不会导致本身的解耦。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Norepinephrine inhibits intercellular coupling in rat cardiomyocytes by ubiquitination of connexin43 gap junctions.

Unlabelled: Gαq-stimulation reduces intercellular coupling within 10 min via a decrease in the membrane lipid phosphatidylinositol-4,5-bisphosphate (PIP2), but the mechanism is unknown. Here we show that uncoupling in rat cardiomyocytes after stimulation of α-adrenergic Gαq-coupled receptors with norepinephrine is prevented by proteasomal and lysosomal inhibitors, suggesting that internalization and possibly degradation of connexin43 (Cx43) is involved. Uncoupling was accompanied by increased Triton X-100 solubility of Cx43, which is considered a measure of the non-junctional pool of Cx43. However, inhibition of the proteasome and lysosome further increased solubility while preserving coupling, suggesting that communicating gap junctions can be part of the soluble fraction. Ubiquitination of Cx43 was also increased, and Cx43 co-immunoprecipitated with the ubiquitin ligase Nedd4.

Conclusions: Norepinephrine increases ubiquitination of Cx43 in cardiomyocytes, possibly via Nedd4. We suggest that Cx43 is subsequently internalized, which is preceded by acquired solubility in Triton X-100, which does not lead to uncoupling per se.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Cell Communication and Adhesion
Cell Communication and Adhesion 生物-生化与分子生物学
CiteScore
2.50
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation Cell Communication and Adhesion is an international Open Access journal which provides a central forum for research on mechanisms underlying cellular signalling and adhesion. The journal provides a single source of information concerning all forms of cellular communication, cell junctions, adhesion molecules and families of receptors from diverse biological systems. The journal welcomes submission of original research articles, reviews, short communications and conference reports.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信