RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes
Autor(a) principal: | |
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Data de Publicação: | 2023 |
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/10773/40272 |
Resumo: | Endo-lysosomes transport along microtubules and clustering in the perinuclear area are two necessary steps for microbes to activate specialized phagocyte functions. We report that RUN and FYVE domain-containing protein 3 (RUFY3) exists as two alternative isoforms distinguishable by the presence of a C-terminal FYVE domain and by their affinity for phosphatidylinositol 3-phosphate on endosomal membranes. The FYVE domain-bearing isoform (iRUFY3) is preferentially expressed in primary immune cells and up-regulated upon activation by microbes and Interferons. iRUFY3 is necessary for ARL8b + /LAMP1+ endo-lysosomes positioning in the pericentriolar organelles cloud of LPS-activated macrophages. We show that iRUFY3 controls macrophages migration, MHC II presentation and responses to Interferon-γ, while being important for intracellular Salmonella replication. Specific inactivation of rufy3 in phagocytes leads to aggravated pathologies in mouse upon LPS injection or bacterial pneumonia. This study highlights the role of iRUFY3 in controlling endo-lysosomal dynamics, which contributes to phagocyte activation and immune response regulation. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytesAnimalsMiceEndosomesLysosomesPhagocytesAntigen presentationLipopolysaccharidesEndo-lysosomes transport along microtubules and clustering in the perinuclear area are two necessary steps for microbes to activate specialized phagocyte functions. We report that RUN and FYVE domain-containing protein 3 (RUFY3) exists as two alternative isoforms distinguishable by the presence of a C-terminal FYVE domain and by their affinity for phosphatidylinositol 3-phosphate on endosomal membranes. The FYVE domain-bearing isoform (iRUFY3) is preferentially expressed in primary immune cells and up-regulated upon activation by microbes and Interferons. iRUFY3 is necessary for ARL8b + /LAMP1+ endo-lysosomes positioning in the pericentriolar organelles cloud of LPS-activated macrophages. We show that iRUFY3 controls macrophages migration, MHC II presentation and responses to Interferon-γ, while being important for intracellular Salmonella replication. Specific inactivation of rufy3 in phagocytes leads to aggravated pathologies in mouse upon LPS injection or bacterial pneumonia. This study highlights the role of iRUFY3 in controlling endo-lysosomal dynamics, which contributes to phagocyte activation and immune response regulation.Nature Research2024-01-23T11:22:09Z2023-07-18T00:00:00Z2023-07-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/40272eng10.1038/s41467-023-40062-xChar, RémyZhuangzhuang LiuJacqueline, CédricDavieau, MarionDelgado, Maria-GracielaSoufflet, ClaraFallet, MathieuChasson, LionelChapuy, RaphaelCamosseto, VoahiranaStrock, EvaRua, RejaneAlmeida, Catarina R.Bing SuLennon-Duménil, Ana-MariaNal, BeatriceRoquilly, AntoineYinming LiangMéresse, StéphaneGatti, EvelinaPierre, Philippeinfo: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:RCAAP2024-05-06T04:51:42Zoai:ria.ua.pt:10773/40272Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-06T04:51:42Repositório 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 |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
title |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
spellingShingle |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes Char, Rémy Animals Mice Endosomes Lysosomes Phagocytes Antigen presentation Lipopolysaccharides |
title_short |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
title_full |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
title_fullStr |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
title_full_unstemmed |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
title_sort |
RUFY3 regulates endolysosomes perinuclear positioning, antigen presentation and migration in activated phagocytes |
author |
Char, Rémy |
author_facet |
Char, Rémy Zhuangzhuang Liu Jacqueline, Cédric Davieau, Marion Delgado, Maria-Graciela Soufflet, Clara Fallet, Mathieu Chasson, Lionel Chapuy, Raphael Camosseto, Voahirana Strock, Eva Rua, Rejane Almeida, Catarina R. Bing Su Lennon-Duménil, Ana-Maria Nal, Beatrice Roquilly, Antoine Yinming Liang Méresse, Stéphane Gatti, Evelina Pierre, Philippe |
author_role |
author |
author2 |
Zhuangzhuang Liu Jacqueline, Cédric Davieau, Marion Delgado, Maria-Graciela Soufflet, Clara Fallet, Mathieu Chasson, Lionel Chapuy, Raphael Camosseto, Voahirana Strock, Eva Rua, Rejane Almeida, Catarina R. Bing Su Lennon-Duménil, Ana-Maria Nal, Beatrice Roquilly, Antoine Yinming Liang Méresse, Stéphane Gatti, Evelina Pierre, Philippe |
author2_role |
author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Char, Rémy Zhuangzhuang Liu Jacqueline, Cédric Davieau, Marion Delgado, Maria-Graciela Soufflet, Clara Fallet, Mathieu Chasson, Lionel Chapuy, Raphael Camosseto, Voahirana Strock, Eva Rua, Rejane Almeida, Catarina R. Bing Su Lennon-Duménil, Ana-Maria Nal, Beatrice Roquilly, Antoine Yinming Liang Méresse, Stéphane Gatti, Evelina Pierre, Philippe |
dc.subject.por.fl_str_mv |
Animals Mice Endosomes Lysosomes Phagocytes Antigen presentation Lipopolysaccharides |
topic |
Animals Mice Endosomes Lysosomes Phagocytes Antigen presentation Lipopolysaccharides |
description |
Endo-lysosomes transport along microtubules and clustering in the perinuclear area are two necessary steps for microbes to activate specialized phagocyte functions. We report that RUN and FYVE domain-containing protein 3 (RUFY3) exists as two alternative isoforms distinguishable by the presence of a C-terminal FYVE domain and by their affinity for phosphatidylinositol 3-phosphate on endosomal membranes. The FYVE domain-bearing isoform (iRUFY3) is preferentially expressed in primary immune cells and up-regulated upon activation by microbes and Interferons. iRUFY3 is necessary for ARL8b + /LAMP1+ endo-lysosomes positioning in the pericentriolar organelles cloud of LPS-activated macrophages. We show that iRUFY3 controls macrophages migration, MHC II presentation and responses to Interferon-γ, while being important for intracellular Salmonella replication. Specific inactivation of rufy3 in phagocytes leads to aggravated pathologies in mouse upon LPS injection or bacterial pneumonia. This study highlights the role of iRUFY3 in controlling endo-lysosomal dynamics, which contributes to phagocyte activation and immune response regulation. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-18T00:00:00Z 2023-07-18 2024-01-23T11:22:09Z |
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/10773/40272 |
url |
http://hdl.handle.net/10773/40272 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1038/s41467-023-40062-x |
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 |
Nature Research |
publisher.none.fl_str_mv |
Nature Research |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817543887971942400 |