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dc.contributor.authorTollersrud, ole kristian
dc.contributor.authorKrausz, Máté
dc.contributor.authorBoehler, Vincent
dc.contributor.authorPolyzou, Aikaterini
dc.contributor.authorSeidl, Maximilian
dc.contributor.authorSpahiu, Ambra
dc.contributor.authorAbdullah, Zeinab
dc.contributor.authorAndryka-Cegielski, Katarzyna
dc.contributor.authorDominick, Felix Immunuel
dc.contributor.authorHuebscher, Katrin
dc.contributor.authorGoschin, Andreas
dc.contributor.authorSmulski, Cristian R.
dc.contributor.authorTrompouki, Eirini
dc.contributor.authorLink, Regina
dc.contributor.authorEbersbach, Hilmar
dc.contributor.authorSrinivas, Honnappa
dc.contributor.authorMarchant, Martine
dc.contributor.authorSogkas, Georgios
dc.contributor.authorStaab, Dieter
dc.contributor.authorVågbø, Cathrine Broberg
dc.contributor.authorGuerini, Danilo
dc.contributor.authorBaasch, Sebastian
dc.contributor.authorLatz, Eicke
dc.contributor.authorHartmann, Gunther
dc.contributor.authorHenneke, Philippe
dc.contributor.authorGeiger, Roger
dc.contributor.authorPeng, Xiao P.
dc.contributor.authorGrimbacher, Bodo
dc.contributor.authorBartok, Eva
dc.contributor.authorAlseth, Ingrun
dc.contributor.authorWarncke, Max
dc.contributor.authorProietti, Michele
dc.date.accessioned2024-11-13T09:07:34Z
dc.date.available2024-11-13T09:07:34Z
dc.date.issued2024-10-22
dc.description.abstractAlthough adenosine deaminase 2 (ADA2) is considered an extracellular ADA, evidence questions the physiological relevance of this activity. Our study reveals that ADA2 localizes within the lysosomes, where it is targeted through modifications of its glycan structures. We show that ADA2 interacts with DNA molecules, altering their sequences by converting deoxyadenosine (dA) to deoxyinosine (dI). We characterize its DNA substrate preferences and provide data suggesting that DNA, rather than free adenosine, is its natural substrate. Finally, we demonstrate that dA-to-dI editing of DNA molecules and ADA2 regulate lysosomal immune sensing of nucleic acids (NAs) by modulating Toll-like receptor 9 (TLR9) activation. Our results describe a mechanism involved in the complex interplay between NA metabolism and immune response, possibly impacting ADA2 deficiency (DADA2) and other diseases involving this pathway, including autoimmune diseases, cancer, or infectious diseases.en_US
dc.identifier.citationTollersrud, Krausz, Boehler, Polyzou, Seidl, Spahiu, Abdullah, Andryka-Cegielski, Dominick, Huebscher, Goschin, Smulski, Trompouki, Link, Ebersbach, Srinivas, Marchant, Sogkas, Staab, Vågbø, Guerini, Baasch, Latz, Hartmann, Henneke, Geiger, Peng, Grimbacher, Bartok, Alseth, Warncke, Proietti. ADA2 is a lysosomal deoxyadenosine deaminase acting on DNA involved in regulating TLR9-mediated immune sensing of DNA. Cell reports. 2024;43(11)en_US
dc.identifier.cristinIDFRIDAID 2318497
dc.identifier.doi10.1016/j.celrep.2024.114899
dc.identifier.issn2211-1247
dc.identifier.urihttps://hdl.handle.net/10037/35680
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalCell reports
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2024 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleADA2 is a lysosomal deoxyadenosine deaminase acting on DNA involved in regulating TLR9-mediated immune sensing of DNAen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Except where otherwise noted, this item's license is described as Attribution 4.0 International (CC BY 4.0)