Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10451/54095 |
Resumo: | Breast cancer (BC) brain metastases is a life-threatening condition to which accounts the poor understanding of BC cells’ (BCCs) extravasation into the brain, precluding the development of preventive strategies. Thus, we aimed to unravel the players involved in the interaction between BCCs and blood–brain barrier (BBB) endothelial cells underlying BBB alterations and the transendothelial migration of malignant cells. We used brain microvascular endothelial cells (BMECs) as a BBB in vitro model, under conditions mimicking shear stress to improve in vivo-like BBB features. Mixed cultures were performed by the addition of fluorescently labelled BCCs to distinguish individual cell populations. BCC–BMEC interaction compromised BBB integrity, as revealed by junctional proteins (β-catenin and zonula occludens-1) disruption and caveolae (caveolin-1) increase, reflecting paracellular and transcellular hyperpermeability, respectively. Both BMECs and BCCs presented alterations in the expression pattern of connexin 43, suggesting the involvement of the gap junction protein. Myosin light chain kinase and phosphorylated myosin light chain were upregulated, revealing the involvement of the endothelial cytoskeleton in the extravasation process. β4-Integrin and focal adhesion kinase were colocalised in malignant cells, reflecting molecular interaction. Moreover, BCCs exhibited invadopodia, attesting migratory properties. Collectively, hub players involved in BC brain metastases formation were unveiled, disclosing possible therapeutic targets for metastases prevention. |
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Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier DisruptionBlood–brain barrierBreast cancer brain metastasesExtravasationParacellular and transcellular migrationAdhesionCellular communicationBreast cancer (BC) brain metastases is a life-threatening condition to which accounts the poor understanding of BC cells’ (BCCs) extravasation into the brain, precluding the development of preventive strategies. Thus, we aimed to unravel the players involved in the interaction between BCCs and blood–brain barrier (BBB) endothelial cells underlying BBB alterations and the transendothelial migration of malignant cells. We used brain microvascular endothelial cells (BMECs) as a BBB in vitro model, under conditions mimicking shear stress to improve in vivo-like BBB features. Mixed cultures were performed by the addition of fluorescently labelled BCCs to distinguish individual cell populations. BCC–BMEC interaction compromised BBB integrity, as revealed by junctional proteins (β-catenin and zonula occludens-1) disruption and caveolae (caveolin-1) increase, reflecting paracellular and transcellular hyperpermeability, respectively. Both BMECs and BCCs presented alterations in the expression pattern of connexin 43, suggesting the involvement of the gap junction protein. Myosin light chain kinase and phosphorylated myosin light chain were upregulated, revealing the involvement of the endothelial cytoskeleton in the extravasation process. β4-Integrin and focal adhesion kinase were colocalised in malignant cells, reflecting molecular interaction. Moreover, BCCs exhibited invadopodia, attesting migratory properties. Collectively, hub players involved in BC brain metastases formation were unveiled, disclosing possible therapeutic targets for metastases prevention.This work was funded by the Portuguese Foundation for Science and Technology (FCT), Portugal, grant numbers PTDC/MED-ONC/29402/2017, UIDP/04138/2020 and UIDB/04138/2020. We also acknowledge FCT financial support of J.G.-P. (SFRH/BD/145522/2019) and of A.R.G. (2020.07115.BD). We acknowledge the Faculty of Sciences of the University of Lisbon’s Microscopy Facility, a node of the Portuguese Platform of BioImaging (PPBI-POCI-01-0145-FEDER-022122). We also acknowledge Luís Marques (Faculty of Sciences, University of Lisbon) for the excellent technical support with image acquisition.MDPIRepositório da Universidade de LisboaPereira, JoanaGarcia, Ana RitaFigueira, InêsMalhó, RuiBrito, Maria Alexandra2022-08-09T17:28:08Z2021-06-302022-06-29T11:35:01Z2021-06-30T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/54095engGodinho-Pereira J, Garcia AR, Figueira I, Malhó R, Brito MA. Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood–Brain Barrier Disruption. International Journal of Molecular Sciences 2021;22:7057. https://doi.org/10.3390/ijms22137057.cv-prod-276345910.3390/ijms22137057info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-08T16:59:24Zoai:repositorio.ul.pt:10451/54095Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:04:29.459334Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
title |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
spellingShingle |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption Pereira, Joana Blood–brain barrier Breast cancer brain metastases Extravasation Paracellular and transcellular migration Adhesion Cellular communication |
title_short |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
title_full |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
title_fullStr |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
title_full_unstemmed |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
title_sort |
Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood Brain Barrier Disruption |
author |
Pereira, Joana |
author_facet |
Pereira, Joana Garcia, Ana Rita Figueira, Inês Malhó, Rui Brito, Maria Alexandra |
author_role |
author |
author2 |
Garcia, Ana Rita Figueira, Inês Malhó, Rui Brito, Maria Alexandra |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Repositório da Universidade de Lisboa |
dc.contributor.author.fl_str_mv |
Pereira, Joana Garcia, Ana Rita Figueira, Inês Malhó, Rui Brito, Maria Alexandra |
dc.subject.por.fl_str_mv |
Blood–brain barrier Breast cancer brain metastases Extravasation Paracellular and transcellular migration Adhesion Cellular communication |
topic |
Blood–brain barrier Breast cancer brain metastases Extravasation Paracellular and transcellular migration Adhesion Cellular communication |
description |
Breast cancer (BC) brain metastases is a life-threatening condition to which accounts the poor understanding of BC cells’ (BCCs) extravasation into the brain, precluding the development of preventive strategies. Thus, we aimed to unravel the players involved in the interaction between BCCs and blood–brain barrier (BBB) endothelial cells underlying BBB alterations and the transendothelial migration of malignant cells. We used brain microvascular endothelial cells (BMECs) as a BBB in vitro model, under conditions mimicking shear stress to improve in vivo-like BBB features. Mixed cultures were performed by the addition of fluorescently labelled BCCs to distinguish individual cell populations. BCC–BMEC interaction compromised BBB integrity, as revealed by junctional proteins (β-catenin and zonula occludens-1) disruption and caveolae (caveolin-1) increase, reflecting paracellular and transcellular hyperpermeability, respectively. Both BMECs and BCCs presented alterations in the expression pattern of connexin 43, suggesting the involvement of the gap junction protein. Myosin light chain kinase and phosphorylated myosin light chain were upregulated, revealing the involvement of the endothelial cytoskeleton in the extravasation process. β4-Integrin and focal adhesion kinase were colocalised in malignant cells, reflecting molecular interaction. Moreover, BCCs exhibited invadopodia, attesting migratory properties. Collectively, hub players involved in BC brain metastases formation were unveiled, disclosing possible therapeutic targets for metastases prevention. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-30 2021-06-30T00:00:00Z 2022-08-09T17:28:08Z 2022-06-29T11:35:01Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10451/54095 |
url |
http://hdl.handle.net/10451/54095 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Godinho-Pereira J, Garcia AR, Figueira I, Malhó R, Brito MA. Behind Brain Metastases Formation: Cellular and Molecular Alterations and Blood–Brain Barrier Disruption. International Journal of Molecular Sciences 2021;22:7057. https://doi.org/10.3390/ijms22137057. cv-prod-2763459 10.3390/ijms22137057 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
MDPI |
publisher.none.fl_str_mv |
MDPI |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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