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A deep-learning framework reveals whole-body perturbations at cell level

dc.contributor.coauthorKaltenecker, D.
dc.contributor.coauthorHorvath, I.
dc.contributor.coauthorAl-Maskari, R.
dc.contributor.coauthorChen, Y.
dc.contributor.coauthorKolabas, Z. I.
dc.contributor.coauthorHoeher, L.
dc.contributor.coauthorTodorov, M.
dc.contributor.coauthorMinde, D.
dc.contributor.coauthorKapoor, S.
dc.contributor.coauthorTurhan, S. G.
dc.contributor.coauthorKuemmerle, L. B.
dc.contributor.coauthorSteinke, H.
dc.contributor.coauthorWohlgemuth, T.
dc.contributor.coauthorAli, M.
dc.contributor.coauthorKofler, F.
dc.contributor.coauthorMorigny, P.
dc.contributor.coauthorGeppert, J.
dc.contributor.coauthorJeridi, D.
dc.contributor.coauthorWittmann, B.
dc.contributor.coauthorLuo, J.
dc.contributor.coauthorShit, S.
dc.contributor.coauthorCigankova, C.
dc.contributor.coauthorKolenic, V. M.
dc.contributor.coauthorGür, N.
dc.contributor.coauthorAydeniz, E.
dc.contributor.coauthorYücecan, A.
dc.contributor.coauthorSimons, L. H. A.
dc.contributor.coauthorPan, C.
dc.contributor.coauthorPiraud, M.
dc.contributor.coauthorRueckert, D.
dc.contributor.coauthorRohm, M.
dc.contributor.coauthorHellal, F.
dc.contributor.coauthorElsner, M.
dc.contributor.coauthorBhatia, H. S.
dc.contributor.coauthorBechmann, I.
dc.contributor.coauthorMenze, B. H.
dc.contributor.coauthorHerzig, S.
dc.contributor.coauthorPaetzold, J. C.
dc.contributor.coauthorDiaz, M. B.
dc.contributor.coauthorErtürk, A.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorErtürk, Ali Maximilian
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-07-17T08:28:30Z
dc.date.issued2026
dc.description.abstractMany diseases, including obesity, have systemic effects that perturb multiple organ systems throughout the body^ 1 , 2 . However, tools for comprehensive, high-resolution analysis of disease-associated changes at the whole-body scale have been lacking. Here we developed MouseMapper, a suite of foundation-model-based deep-learning algorithms enabling multi-system analysis of disease across the entire mouse body. MouseMapper enables whole-body quantitative analysis of nerves and immune cells, resolving fine axonal branches and immune-cell clusters while automatically segmenting 31 organs and tissues. We used MouseMapper to study diet-induced obesity, and identified structural alterations of the infraorbital branch of the trigeminal ganglia. This structural impairment in infraorbital nerves was associated with functional sensory deficits in whisker sensing. Furthermore, we identified proteomic changes in the trigeminal ganglion affecting axon remodelling and complement pathways both in mice and humans. MouseMapper also generated detailed three-dimensional inflammation maps by characterizing immune cell cluster compositions across tissues. The MouseMapper framework demonstrates robust generalizability across different imaging resolutions and datasets. Our study provides a powerful, scalable approach for identifying and quantifying systemic pathologies, bridging molecular insights from animal models to human conditions. An analysis of diet-induced obesity using MouseMapper—a suite of foundation-model-based deep-learning algorithms—identifies structural alterations of the infraorbital branch of the trigeminal ganglia.
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuEU
dc.description.sponsorshipWe thank L. Mehr, D. Ha\u00DF, R. T. Exp\u00F3sito, A. Gr\u00FCttner and K. Lohr for technical and operational support. Figures , and were created in BioRender. Parts of Extended Data Fig. were created in draw.io. This work was supported by the Vascular Dementia Research Foundation, Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany\u2019s Excellence Strategy within the framework of the Munich Cluster for Systems Neurology (EXC 2145 SyNergy, grant 390857198) and DFG (grants SFB 1052, project A9; TR 296 project 03) as well as the German Federal Ministry of Education and Research (Bundesministerium f\u00FCr Bildung und Forschung) within the NATON collaboration (grant 01KX2121) and the HIVacToGC collaboration. A.E. received support through the European Research Council Consolidator grant (CALVARIA, grant GA 865323), Nomis Heart Atlas Project Grant (Nomis Foundation), the Helmholtz Imaging Platform - FOMIA (ZT-I-PF-4-091) and a collaborative research centre grant (CRC1744, DFG, German Research Foundation). D.K. was supported by EFSD and Novo Nordisk A/S Programme for Diabetes Research in Europe. Y.C. was supported by the China Scholarship Council for the PhD study. This work was supported by the European Research Council under the European Union\u2019s Horizon 2020 research and innovation program (949017 to M.R.) and a grant from the Else-Kr\u00F6ner-Fresenius-Stiftung (2020 EKSE.23 to S.H.), as well as the Edith-Haberland-Wagner Stiftung. B.H.M and B.W. acknowledge support by the Helmut Horten Foundation and C.P. acknowledges the Edith-Haberland-Wagner Stiftung and Shanghai Basic Research Pioneer Project. F.K. acknowledges Gemeinn\u00FCtzige Hertie Stiftung.
dc.description.versionPublished Version
dc.identifier.ScopusPercentile99
dc.identifier.ScopusQuartileQ1
dc.identifier.WoSPercentile99.6
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.1038/s41586-026-10535-2
dc.identifier.eissn1476-4687
dc.identifier.embargoN/A
dc.identifier.endpage11
dc.identifier.grantnoGA 865323
dc.identifier.grantno949017
dc.identifier.issn0028-0836
dc.identifier.pubmed42162424
dc.identifier.scopus2-s2.0-105039684383
dc.identifier.startpage1
dc.identifier.urihttp://doi.org/10.1038/s41586-026-10535-2
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33379
dc.identifier.wos001771187200001
dc.keywordsTrigeminal ganglion
dc.keywordsAxon
dc.keywordsInfraorbital nerve
dc.keywordsTrigeminal nerve
dc.keywordsSensory system
dc.keywordsSemaphorin
dc.keywordsImmune system
dc.keywordsAfferent
dc.languageeng
dc.publisherNature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNature
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectGenetics and molecular biology
dc.subjectMolecular biology
dc.subjectNeuroscience
dc.subjectNeurology
dc.subjectBiophysics
dc.titleA deep-learning framework reveals whole-body perturbations at cell level
dc.typeJournal Article
dspace.entity.typePublication
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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