Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/271569 |
Resumo: | S100B, a homodimeric Ca2+-binding protein, is produced and secreted by astrocytes, and its extracellular levels have been used as a glial marker in brain damage and neurodegenerative and psychiatric diseases; however, its mechanism of secretion is elusive. We used primary astrocyte cultures and calcium measurements from real-time fluorescence microscopy to investigate the role of intracellular calcium in S100B secretion. In addition, the dimethyl sulfoxide (DMSO) effect on S100B was investigated in vitro and in vivo using Wistar rats. We found that DMSO, a widely used vehicle in biological assays, is a powerful S100B secretagogue, which caused a biphasic response of Ca2+ mobilization. Our data show that astroglial S100B secretion is triggered by the increase in intracellular Ca2+ and indicate that this increase is due to Ca2+ mobilization from the endoplasmic reticulum. Also, blocking plasma membrane Ca2+ channels involved in the Ca2+ replenishment of internal stores decreased S100B secretion. The DMSO-induced S100B secretion was confirmed in vivo and in ex vivo hippocampal slices. Our data support a nonclassic vesicular export of S100B modulated by Ca2+, and the results might contribute to understanding the mechanism underlying the astroglial release of S100B. |
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Leite, Marina ConcliGalland, Fabiana Andrea BarreraGuerra, Maria Cristina Azambuja Barea da SilveiraRodrigues, LetíciaTaday, Jéssica HauschildMonteforte, Priscila TotarelliHirata, HanakoGottfried, Carmem Juracy SilveiraDonato, RosárioSmaili, Soraya SoubhiGoncalves, Carlos Alberto Saraiva2024-02-06T04:31:53Z20231422-0067http://hdl.handle.net/10183/271569001193421S100B, a homodimeric Ca2+-binding protein, is produced and secreted by astrocytes, and its extracellular levels have been used as a glial marker in brain damage and neurodegenerative and psychiatric diseases; however, its mechanism of secretion is elusive. We used primary astrocyte cultures and calcium measurements from real-time fluorescence microscopy to investigate the role of intracellular calcium in S100B secretion. In addition, the dimethyl sulfoxide (DMSO) effect on S100B was investigated in vitro and in vivo using Wistar rats. We found that DMSO, a widely used vehicle in biological assays, is a powerful S100B secretagogue, which caused a biphasic response of Ca2+ mobilization. Our data show that astroglial S100B secretion is triggered by the increase in intracellular Ca2+ and indicate that this increase is due to Ca2+ mobilization from the endoplasmic reticulum. Also, blocking plasma membrane Ca2+ channels involved in the Ca2+ replenishment of internal stores decreased S100B secretion. The DMSO-induced S100B secretion was confirmed in vivo and in ex vivo hippocampal slices. Our data support a nonclassic vesicular export of S100B modulated by Ca2+, and the results might contribute to understanding the mechanism underlying the astroglial release of S100B.application/pdfengInternational journal of molecular sciences. Basel. Vol. 24, no. 23 (Dec. 2023), 16576, 18 p.Sistema nervosoAstrócitosDoenças neurodegenerativasProteínas de ligação ao cálcioS100B secretionCalcium signalingAstrocytesAstroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagoguesEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001193421.pdf.txt001193421.pdf.txtExtracted Texttext/plain8315http://www.lume.ufrgs.br/bitstream/10183/271569/2/001193421.pdf.txt7dede64920ad2781fd28a1e7e254a10dMD52ORIGINAL001193421.pdfTexto completo (inglês)application/pdf77809http://www.lume.ufrgs.br/bitstream/10183/271569/1/001193421.pdf741ba0320b30e4fe48f5cfdb8dad58feMD5110183/2715692024-02-07 06:01:35.623593oai:www.lume.ufrgs.br:10183/271569Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-02-07T08:01:35Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
title |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
spellingShingle |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues Leite, Marina Concli Sistema nervoso Astrócitos Doenças neurodegenerativas Proteínas de ligação ao cálcio S100B secretion Calcium signaling Astrocytes |
title_short |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
title_full |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
title_fullStr |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
title_full_unstemmed |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
title_sort |
Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues |
author |
Leite, Marina Concli |
author_facet |
Leite, Marina Concli Galland, Fabiana Andrea Barrera Guerra, Maria Cristina Azambuja Barea da Silveira Rodrigues, Letícia Taday, Jéssica Hauschild Monteforte, Priscila Totarelli Hirata, Hanako Gottfried, Carmem Juracy Silveira Donato, Rosário Smaili, Soraya Soubhi Goncalves, Carlos Alberto Saraiva |
author_role |
author |
author2 |
Galland, Fabiana Andrea Barrera Guerra, Maria Cristina Azambuja Barea da Silveira Rodrigues, Letícia Taday, Jéssica Hauschild Monteforte, Priscila Totarelli Hirata, Hanako Gottfried, Carmem Juracy Silveira Donato, Rosário Smaili, Soraya Soubhi Goncalves, Carlos Alberto Saraiva |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Leite, Marina Concli Galland, Fabiana Andrea Barrera Guerra, Maria Cristina Azambuja Barea da Silveira Rodrigues, Letícia Taday, Jéssica Hauschild Monteforte, Priscila Totarelli Hirata, Hanako Gottfried, Carmem Juracy Silveira Donato, Rosário Smaili, Soraya Soubhi Goncalves, Carlos Alberto Saraiva |
dc.subject.por.fl_str_mv |
Sistema nervoso Astrócitos Doenças neurodegenerativas Proteínas de ligação ao cálcio |
topic |
Sistema nervoso Astrócitos Doenças neurodegenerativas Proteínas de ligação ao cálcio S100B secretion Calcium signaling Astrocytes |
dc.subject.eng.fl_str_mv |
S100B secretion Calcium signaling Astrocytes |
description |
S100B, a homodimeric Ca2+-binding protein, is produced and secreted by astrocytes, and its extracellular levels have been used as a glial marker in brain damage and neurodegenerative and psychiatric diseases; however, its mechanism of secretion is elusive. We used primary astrocyte cultures and calcium measurements from real-time fluorescence microscopy to investigate the role of intracellular calcium in S100B secretion. In addition, the dimethyl sulfoxide (DMSO) effect on S100B was investigated in vitro and in vivo using Wistar rats. We found that DMSO, a widely used vehicle in biological assays, is a powerful S100B secretagogue, which caused a biphasic response of Ca2+ mobilization. Our data show that astroglial S100B secretion is triggered by the increase in intracellular Ca2+ and indicate that this increase is due to Ca2+ mobilization from the endoplasmic reticulum. Also, blocking plasma membrane Ca2+ channels involved in the Ca2+ replenishment of internal stores decreased S100B secretion. The DMSO-induced S100B secretion was confirmed in vivo and in ex vivo hippocampal slices. Our data support a nonclassic vesicular export of S100B modulated by Ca2+, and the results might contribute to understanding the mechanism underlying the astroglial release of S100B. |
publishDate |
2023 |
dc.date.issued.fl_str_mv |
2023 |
dc.date.accessioned.fl_str_mv |
2024-02-06T04:31:53Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/271569 |
dc.identifier.issn.pt_BR.fl_str_mv |
1422-0067 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001193421 |
identifier_str_mv |
1422-0067 001193421 |
url |
http://hdl.handle.net/10183/271569 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
International journal of molecular sciences. Basel. Vol. 24, no. 23 (Dec. 2023), 16576, 18 p. |
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info:eu-repo/semantics/openAccess |
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openAccess |
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