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Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP

Connexins are membrane proteins that form GJ (gap junction) channels between adjacent cells. Cx43 (connexin 43), the most widely expressed member of the connexin family, has a rapid turnover rate, and its degradation involves both the lysosomal and ubiquitin–proteasome pathway. The goal of this work...

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Autores principales: Rangel, Marisa, Ionta, Marisa, Cristina Pfister, Sandra, Adolpho Sant’Anna Ferreira, Raphael, Maria Machado-Santelli, Glaucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476824/
https://www.ncbi.nlm.nih.gov/pubmed/23119141
http://dx.doi.org/10.1042/CBR20100003
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author Rangel, Marisa
Ionta, Marisa
Cristina Pfister, Sandra
Adolpho Sant’Anna Ferreira, Raphael
Maria Machado-Santelli, Glaucia
author_facet Rangel, Marisa
Ionta, Marisa
Cristina Pfister, Sandra
Adolpho Sant’Anna Ferreira, Raphael
Maria Machado-Santelli, Glaucia
author_sort Rangel, Marisa
collection PubMed
description Connexins are membrane proteins that form GJ (gap junction) channels between adjacent cells. Cx43 (connexin 43), the most widely expressed member of the connexin family, has a rapid turnover rate, and its degradation involves both the lysosomal and ubiquitin–proteasome pathway. The goal of this work was to study the effects of geodiamolides, natural peptides from marine sponge that normally are involved with microfilament disruption, on connexin assembly or degradation in the plasma membrane. HTC (hepatocarcinoma cells) expressing Cx43–GFP (green fluorescent protein) were submitted to treatment with 200 nM geodiamolides A, B, H and I for 2 and 4 h. Microfilament distribution and the presence and size of GJ plaques were evaluated by laser scanning confocal microscopy. Among the four peptides tested, only Geo H (geodiamolide H) statistically enhanced the length of GJ plaques. Geodiamolide A also showed activity in the GJ plaque size; however, its effect was less pronounced. Treatment with Geo H could interfere with the delivery of connexins to the degradation structures, similar to proteasomal pathways, keeping the connexins assembled and accumulating GJ plaques. Further experiments, with the cells treated with Geo H, using the fungal antibiotic BFA (brefeldin A), were performed in order to uncouple events leading to GJ assembly from those related to GJ removal, since BFA is known to block protein trafficking within a fused ER (endoplasmic reticulum)/Golgi compartment. GJ plaques were drastically reduced after BFA/Geo H treatment, thus indicating that Geo H affects mainly the delivery pathway of Cx43 protein.
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spelling pubmed-34768242012-10-30 Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP Rangel, Marisa Ionta, Marisa Cristina Pfister, Sandra Adolpho Sant’Anna Ferreira, Raphael Maria Machado-Santelli, Glaucia Cell Biol Int Rep (2010) Research Article Connexins are membrane proteins that form GJ (gap junction) channels between adjacent cells. Cx43 (connexin 43), the most widely expressed member of the connexin family, has a rapid turnover rate, and its degradation involves both the lysosomal and ubiquitin–proteasome pathway. The goal of this work was to study the effects of geodiamolides, natural peptides from marine sponge that normally are involved with microfilament disruption, on connexin assembly or degradation in the plasma membrane. HTC (hepatocarcinoma cells) expressing Cx43–GFP (green fluorescent protein) were submitted to treatment with 200 nM geodiamolides A, B, H and I for 2 and 4 h. Microfilament distribution and the presence and size of GJ plaques were evaluated by laser scanning confocal microscopy. Among the four peptides tested, only Geo H (geodiamolide H) statistically enhanced the length of GJ plaques. Geodiamolide A also showed activity in the GJ plaque size; however, its effect was less pronounced. Treatment with Geo H could interfere with the delivery of connexins to the degradation structures, similar to proteasomal pathways, keeping the connexins assembled and accumulating GJ plaques. Further experiments, with the cells treated with Geo H, using the fungal antibiotic BFA (brefeldin A), were performed in order to uncouple events leading to GJ assembly from those related to GJ removal, since BFA is known to block protein trafficking within a fused ER (endoplasmic reticulum)/Golgi compartment. GJ plaques were drastically reduced after BFA/Geo H treatment, thus indicating that Geo H affects mainly the delivery pathway of Cx43 protein. Portland Press Ltd 2010-08-11 /pmc/articles/PMC3476824/ /pubmed/23119141 http://dx.doi.org/10.1042/CBR20100003 Text en © The Author(s). http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commerical use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rangel, Marisa
Ionta, Marisa
Cristina Pfister, Sandra
Adolpho Sant’Anna Ferreira, Raphael
Maria Machado-Santelli, Glaucia
Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title_full Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title_fullStr Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title_full_unstemmed Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title_short Marine sponge depsipeptide increases gap junction length in HTC cells transfected with Cx43–GFP
title_sort marine sponge depsipeptide increases gap junction length in htc cells transfected with cx43–gfp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476824/
https://www.ncbi.nlm.nih.gov/pubmed/23119141
http://dx.doi.org/10.1042/CBR20100003
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