Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells
[Introduction]: HIV-1 exploits dendritic cells (DCs) to spread throughout the body via specific recognition of gangliosides present on the viral envelope by the CD169/Siglec-1 membrane receptor. This interaction triggers the internalization of HIV-1 within a structure known as the sac-like compartme...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/379551 |
| Acceso en línea: | http://hdl.handle.net/10261/379551 |
| Access Level: | acceso abierto |
| Palabra clave: | Dendritic cells CD169/Siglec1 HIV Sac-like compartment MEND |
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Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cellsLaguía, FernandoChojnacki, JakubErkizia, ItziarGeli, María IsabelEnrich, CarlosMartinez-Picado. JavierResa-Infante, PatriciaDendritic cellsCD169/Siglec1HIVSac-like compartmentMEND[Introduction]: HIV-1 exploits dendritic cells (DCs) to spread throughout the body via specific recognition of gangliosides present on the viral envelope by the CD169/Siglec-1 membrane receptor. This interaction triggers the internalization of HIV-1 within a structure known as the sac-like compartment. While the mechanism underlying sac-like compartment formation remains elusive, prior research indicates that the process is clathrin-independent and cell membrane cholesterol–dependent and involves transient disruption of cortical actin. Here, we investigate the potential involvement of massive endocytosis (MEND) in this process.[Methods]: We used live cell confocal imaging to measure the dimensions and dynamics of the compartment. We assessed the role of actin and cholesterol in fixed and live cells using confocal microscopy and evaluated the effect of PI3K and protein palmytoilation inhibitors during viral uptake.[Results]: Our data demonstrate extensive plasma membrane invagination based on sac-like compartment dimensions (2.9 μm in diameter and 20 μm3 in volume). We showed that the cholesterol concentration doubles within the regions of viral uptake, suggesting lipid-phase separation, and that development of the sac-like compartment is accompanied by transient depolarization of cortical actin. Moreover, we observed that protein palmitoylation and PI3K inhibition reduce the sac-like compartment formation rate from 70% to 20% and 40%, respectively.[Conclusions]: Our results indicate the involvement of MEND mechanisms during sac-like compartment formation.The authors’ laboratories were supported by funding from the Spanish Ministry of Science and Innovation (grants PID2022-139271OB-I00 and CB21/13/00063, Spain), NIH/NIAID (1UM1AI164561-01 and 1P01AI178376-01, United States of America), Generalitat de València (grant PROMETEO/2021/036, Spain), and Grifols (Spain).Peer reviewedFrontiers MediaMinisterio de Ciencia e Innovación (España)Agencia Estatal de Investigación (España)National Institutes of Health (US)National Institute of Allergy and Infectious Diseases (US)Generalitat ValencianaGrifolsConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]202520252024info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501Publisher's versioninfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10261/379551reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Inglés#PLACEHOLDER_PARENT_METADATA_VALUE#info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-139271OB-I00The underlying dataset has been published as supplementary material of the article in the publisher platform at DOI https://doi.org/10.3389/fimmu.2024.1505840https://doi.org/10.3389/fimmu.2024.1505840Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/3795512026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| title |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| spellingShingle |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells Laguía, Fernando Dendritic cells CD169/Siglec1 HIV Sac-like compartment MEND |
| title_short |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| title_full |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| title_fullStr |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| title_full_unstemmed |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| title_sort |
Massive endocytosis mechanisms are involved in uptake of HIV-1 particles by monocyte-derived dendritic cells |
| dc.creator.none.fl_str_mv |
Laguía, Fernando Chojnacki, Jakub Erkizia, Itziar Geli, María Isabel Enrich, Carlos Martinez-Picado. Javier Resa-Infante, Patricia |
| author |
Laguía, Fernando |
| author_facet |
Laguía, Fernando Chojnacki, Jakub Erkizia, Itziar Geli, María Isabel Enrich, Carlos Martinez-Picado. Javier Resa-Infante, Patricia |
| author_role |
author |
| author2 |
Chojnacki, Jakub Erkizia, Itziar Geli, María Isabel Enrich, Carlos Martinez-Picado. Javier Resa-Infante, Patricia |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Ministerio de Ciencia e Innovación (España) Agencia Estatal de Investigación (España) National Institutes of Health (US) National Institute of Allergy and Infectious Diseases (US) Generalitat Valenciana Grifols Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| dc.subject.none.fl_str_mv |
Dendritic cells CD169/Siglec1 HIV Sac-like compartment MEND |
| topic |
Dendritic cells CD169/Siglec1 HIV Sac-like compartment MEND |
| description |
[Introduction]: HIV-1 exploits dendritic cells (DCs) to spread throughout the body via specific recognition of gangliosides present on the viral envelope by the CD169/Siglec-1 membrane receptor. This interaction triggers the internalization of HIV-1 within a structure known as the sac-like compartment. While the mechanism underlying sac-like compartment formation remains elusive, prior research indicates that the process is clathrin-independent and cell membrane cholesterol–dependent and involves transient disruption of cortical actin. Here, we investigate the potential involvement of massive endocytosis (MEND) in this process. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 2025 2025 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 Publisher's version info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10261/379551 |
| url |
http://hdl.handle.net/10261/379551 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
#PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2022-139271OB-I00 The underlying dataset has been published as supplementary material of the article in the publisher platform at DOI https://doi.org/10.3389/fimmu.2024.1505840 https://doi.org/10.3389/fimmu.2024.1505840 Sí |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Frontiers Media |
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Frontiers Media |
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reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC instname:Consejo Superior de Investigaciones Científicas (CSIC) |
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Consejo Superior de Investigaciones Científicas (CSIC) |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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DIGITAL.CSIC. Repositorio Institucional del CSIC |
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