Endolysosomal vesicles at the center of B cell activation

dc.contributor.authorHämälistö, Saara
dc.contributor.authorBatalla
dc.contributor.authorValle del Felipe
dc.contributor.authorYuseff Isabel, María
dc.contributor.authorMattila, Pieta
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id380834693
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/380834693
dc.date.accessioned2025-08-27T21:34:52Z
dc.date.available2025-08-27T21:34:52Z
dc.description.abstract<p>The endolysosomal system specializes in degrading cellular components and is crucial to maintaining homeostasis and adapting rapidly to metabolic and environmental cues. Cells of the immune system exploit this network to process antigens or promote cell death by secreting lysosome-related vesicles. In B lymphocytes, lysosomes are harnessed to facilitate the extraction of antigens and to promote their processing into peptides for presentation to T cells, critical steps to mount protective high-affinity antibody responses. Intriguingly, lysosomal vesicles are now considered important signaling units within cells and also display secretory functions by releasing their content to the extracellular space. In this review, we focus on how B cells use pathways involved in the intracellular trafficking, secretion, and function of endolysosomes to promote adaptive immune responses. A basic understanding of such mechanisms poses an interesting frontier for the development of therapeutic strategies in the context of cancer and autoimmune diseases.<br></p>
dc.identifier.eissn1540-8140
dc.identifier.jour-issn0021-9525
dc.identifier.olddbid200660
dc.identifier.oldhandle10024/183687
dc.identifier.urihttps://www.utupub.fi/handle/11111/46635
dc.identifier.urlhttps://doi.org/10.1083/jcb.202307047
dc.identifier.urnURN:NBN:fi-fe2025082789191
dc.language.isoen
dc.okm.affiliatedauthorHämälistö, Saara
dc.okm.affiliatedauthorMattila, Pieta
dc.okm.affiliatedauthorDataimport, MediCity
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherRockefeller University Press
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumbere202307047
dc.relation.doi10.1083/jcb.202307047
dc.relation.ispartofjournalJournal of Cell Biology
dc.relation.issue3
dc.relation.volume223
dc.source.identifierhttps://www.utupub.fi/handle/10024/183687
dc.titleEndolysosomal vesicles at the center of B cell activation
dc.year.issued2024

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