Astroglial S100B secretion is mediated by Ca2+ mobilization from endoplasmic reticulum : a study using forskolin and DMSO as secretagogues

Detalhes bibliográficos
Autor(a) principal: Leite, Marina Concli
Data de Publicação: 2023
Outros Autores: 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
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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spelling 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
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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
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url http://hdl.handle.net/10183/271569
dc.language.iso.fl_str_mv eng
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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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