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Stein"],"technology_type":["Data-dependent acquisition","Mass Spectrometry"],"software":[""],"submitter_keywords":["Fcyriiia","Slan+ non-classical monocytes","Cd16a","Immune complexes","Migration","Slanmo","Haptokinesis"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD079927"],"tissue":["Primary Cell","Monocyte"],"sample_protocol":["Slan+ non-classical monocytes were seeded onto immobilized immune complexes and incubated at 37°C for 2h. As reference,  Slan+ non-classical monocytes from the same donor were incubated on uncoated culture dishes for 2h and cells were then  harvested from tissue culture dishes. Cells were lysed in urea-based lysis buffer containing phosphatase and protease inhibitors. Lysates were sonicated, cleared by centrifugation, and protein concentrations were determined. Proteins were precipitated by methanol/chloroform extraction, resuspended in HEPES/SDC buffer, reduced and alkylated, and digested overnight with trypsin. Peptides were desalted using Oasis HLB cartridges. Phosphopeptides were enriched using Fe-NTA magnetic beads on a KingFisher Apex platform. Enriched phosphopeptides were TMT10plex labeled, pooled, fractionated by high-pH reversed-phase chromatography, and analyzed by LC-MS/MS on an Orbitrap Fusion Lumos mass spectrometer."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["Raw files were converted to mzML format using ProteoWizard MSConvert and searched using MSFragger in FragPipe v20 against the Homo sapiens UniProt reference proteome (UP000005640) including common contaminants and decoy sequences. Carbamidomethylation and TMT10 labeling were specified as fixed modifications, while oxidation, acetylation, TMT10 N-terminal labeling, and phosphorylation (STY) were included as variable modifications where appropriate. Peptide and protein false discovery rates were controlled at 1%. Downstream data processing and statistical analyses were performed in R. Batch effects were removed using limma, normalization was performed using variance stabilization normalization (VSN), and differential expression analysis was conducted using moderated t-tests implemented in limma."],"omics_type":["Proteomics"],"labhead":["Knut Schäkel"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Universitäts Hautklinik Heidelberg"],"species":["Homo Sapiens (human)"],"publication":["10.1016/J.JAUT.2026.103579","42288023 Hertwig M, Oehrl S, Döbel T, Zhang H, Meisel S, List A, Schäkel K. A gradient of immune complexes induces directional migration and a lupus-associated transcriptional program in Slan&lt;sup&gt;+&lt;/sup&gt; non-classical monocytes. J Autoimmun. 2026 162:103579 10.1016/j.jaut.2026.103579"],"submitter_mail":["frank.stein@embl.de"],"submitter_affiliation":["EMBL"],"submitter_country":["Germany"],"pubmed_abstract":["Immune complexes (ICs) play a central role in autoimmune diseases, where they accumulate in tissues, activate Fc gamma receptor-expressing cells, and promote chronic inflammation. However, the role of ICs as directional migratory cues for human leukocytes remains poorly defined. Here, we identify pro-inflammatory Slan + non-classical monocytes (SlanMo), a CD14<sup>dim</sup> CD16<sup>++</sup> monocyte subset, as the only blood leukocyte population that migrates directionally toward ICs. Using in vitro transmigration assays, we demonstrate that SlanMo respond to ICs in a concentration-dependent, gradient-dependent, and CD16-mediated manner. Strikingly, SlanMo follow IC gradients with high specificity, enabling their active and directed migration towards high concentrations of ICs. This migration is independent of G protein-coupled receptor signaling, and is, therefore, not dependent on chemokines. Guided by our phosphoproteomic analysis of migrating SlanMo, we identified ROCK, Lyn, crk, FAK, and moesin as relevant signaling proteins. Our transcriptomic profiling of SlanMo after migration on immobilized ICs versus uncoated surfaces revealed enrichment of pathways linked to SLE as well as an upregulation of genes associated with antigen processing, endocytosis, and protein digestion. These findings suggest that ICs can act as directional cues for selective leukocyte recruitment of pro-inflammatory SlanMo which may be of relevance in IC-rich environments such as in SLE."],"pubmed_title":["A gradient of immune complexes induces directional migration and a lupus-associated transcriptional program in Slan&lt;sup&gt;+&lt;/sup&gt; non-classical monocytes."],"pubmed_authors":["Hertwig Michael M, Oehrl Stephanie S, Döbel Thomas T, Zhang Hao H, Meisel Stefan S, List Amelie A, Schäkel Knut K"],"additional_accession":[]},"is_claimable":false,"name":"Immune Complex-Induced Migration of Slan+ Non-Classical Monocytes","description":"Slan+ Non-Classical Monocytes migrate on immobilized immune complexes. This phenomenon can be blcoked with anti-CD16 blocking antibodies and is therefore thought to be mediated via CD16 (FcyRIII). Nonetheless, other CD16+ cells, such as NK cells or neutrophils, as well as lineage related cells suchs as classical monocytes do not migrate on immobilized immune complexes. We therefore isolated protein content of Slan+ Non-Classical Monocytes after migration immobilized immune complexes to perform phosphoproteomics in order to better understand the underlying signaling pathways inducing the migratory response.","dates":{"publication":"2026-07-09","submission":"2026-06-19"},"accession":"PXD079927","cross_references":{"TAXONOMY":["NEWT:3555","NEWT:71647","NEWT:330879","NEWT:35554","NEWT:32046","NEWT:544496","NEWT:2042546","NEWT:32049","NEWT:1392696","NEWT:259447","NEWT:295546","NEWT:45351","NEWT:445974","NEWT:43179","NEWT:180454","NEWT:5722","NCBITaxon:1280","NEWT:1129","NEWT:309807","NEWT:55153","NEWT:309800","NEWT:281395","NEWT:1211601","NEWT:876138","NEWT:44271","NEWT:43186","NEWT:10036","NEWT:1590","NEWT:498019","NEWT:1351","NEWT:1438992","NEWT:1352","NEWT:2649997","NEWT:1147161","NEWT:638632","NEWT:263737","NEWT:224326","NEWT:1333499","NCBITaxon:79857","NEWT:1096976","NEWT:5702","NEWT:95648","NEWT:1589","NEWT:135622","NEWT:1349","NEWT:96731","NEWT:383379","NEWT:418106","NEWT:10029","NEWT:913645","NEWT:44491","NEWT:641809","NEWT:27933","NEWT:556484","NEWT:317447","NEWT:4688","NEWT:7955","NEWT:7959","NEWT:2261","NEWT:31156","NEWT:3112","NEWT:79329","NEWT:4442","NEWT:192875","NEWT:1214915","NEWT:12637","NEWT:59729","NEWT:2164133","NEWT:108061","NEWT:60711","NEWT:1316931","NEWT:224308","NEWT:3347","NEWT:511145","NEWT:160621","NEWT:212790","NEWT:931281","NEWT:4432","NEWT:5762","NEWT:658457","NEWT:1310161","NEWT:77133","NEWT:295358","NEWT:145481","NCBITaxon:79824","NEWT:2246","NEWT:2652724","NCBITaxon:4563","NEWT:5755","NEWT:44689","NEWT:44447","NEWT:752555","NEWT:498211","NEWT:5759","NEWT:1736231","NEWT:5518","NEWT:398007","NEWT:1392","NEWT:498217","NEWT:498216","NEWT:2242","NEWT:11320","NEWT:286","NEWT:391619","NEWT:246196","NEWT:287","NEWT:246197","NEWT:1367269","NEWT:633149","NEWT:10239","NEWT:44685","NEWT:161934","NEWT:4897","NEWT:1148","NEWT:5744","NEWT:5508","NEWT:3329","NEWT:5507","NEWT:410661","NEWT:55571","NEWT:35500","NEWT:1235816","NEWT:1140","NCBITaxon:2157","NEWT:1143","NEWT:4896","NEWT:1287689","NEWT:1390","NEWT:11557","NEWT:1094343","NEWT:1462472","NEWT:1336795","NEWT:644042","NEWT:294","NEWT:1773","NEWT:1182590","NEWT:3712","NEWT:82380","NEWT:3711","NEWT:935293","NEWT:375146","NEWT:2065263","NEWT:118698","NEWT:1616117","NEWT:263","NEWT:118696","NEWT:52283","NEWT:284812","NEWT:8175","NEWT:43330","NEWT:1603293","NEWT:408169","NEWT:44664","NEWT:47946","NEWT:3702","NEWT:243277","NEWT:1246791","NEWT:7067","NEWT:118694","NEWT:2850","NEWT:118691","NEWT:33548","NEWT:274","NEWT:7070","NEWT:408172","NEWT:408170","NEWT:96794","NEWT:3708","NEWT:332648","NEWT:44670","NEWT:536231","NEWT:376219","NEWT:219813","NEWT:1436733","NEWT:460519","NEWT:1247411","NEWT:572307","NEWT:1432138","NEWT:1424507","NEWT:1194599","NEWT:272844","NEWT:9483","NEWT:333760","NEWT:1513458","NEWT:1233681","NCBITaxon:40559","NEWT:506599","NEWT:2853422","NEWT:84588","NEWT:1679718","NEWT:480","NEWT:65349","NEWT:67767","NEWT:46835","NEWT:109757","NEWT:582580","NEWT:300852","NEWT:1502","NEWT:376686","NEWT:95486","NEWT:508771","NEWT:1883446","NEWT:253","NCBITaxon:2759","NEWT:1233435","NEWT:93061","NEWT:93062","NCBITaxon:4932","NEWT:109760","NEWT:943274","NEWT:644223","NEWT:235443","NEWT:108458","NEWT:5936","NEWT:272623","NEWT:272624","NEWT:320637","NEWT:983964","NEWT:118499","NEWT:11706","NEWT:32644","NEWT:527796","NEWT:55529","NEWT:499175","NEWT:109779","NEWT:3745","NEWT:1715989","NCBITaxon:4751","NEWT:476272","NEWT:3747","NEWT:195051","NEWT:3988","NEWT:1116234","NEWT:1255228","NEWT:649908","NEWT:410289","NEWT:373153","NEWT:3983","NEWT:352472","NEWT:1071661","NEWT:1202532","NEWT:360094","NEWT:470","NEWT:41364","NEWT:1313","NEWT:1218097","NEWT:39491","NCBITaxon:5811","NEWT:29491","NEWT:2014887","NEWT:33952","NEWT:153009","NEWT:261756","NEWT:571256","NEWT:40483","NEWT:63366","NEWT:63367","NEWT:215402","NCBITaxon:548681","NEWT:272634","NEWT:9031","NEWT:1872122","NEWT:7091","NEWT:1034015","NEWT:141262","NEWT:108931","NEWT:1055524","NEWT:4087","NEWT:9778","NEWT:306","NEWT:150475","NEWT:303","NEWT:267872","NEWT:7111","NEWT:347515","NEWT:9534","NEWT:5180","NEWT:256737","NEWT:4090","NEWT:4092","NEWT:9541","NEWT:8694","NEWT:4093","NEWT:4096","NEWT:8692","NEWT:2903","NEWT:185579","NEWT:941442","NEWT:536088","NEWT:13076","NEWT:1226408","NEWT:7108","NEWT:40479","NEWT:43989","NEWT:4076","NEWT:142615","NEWT:317","NEWT:1006581","NEWT:885318","NEWT:39488","NEWT:550","NEWT:4081","NEWT:273068","NEWT:554","NEWT:98334","NEWT:451516","NEWT:4084","NEWT:63577","NEWT:36185","NEWT:1225786","NEWT:7574","NEWT:1715256","NEWT:30640","NEWT:575412","NEWT:929793","NEWT:29204","NEWT:28112","NEWT:114155","NEWT:6494","NEWT:6491","NEWT:507601","NEWT:186441","NEWT:643680","NEWT:214092","NCBITaxon:6157","NEWT:6239","NEWT:162425","NEWT:216257","NEWT:102169","NEWT:9986","NEWT:4054","NEWT:8654","NEWT:8658","NEWT:1268063","NEWT:8655","NEWT:98351","NEWT:1263854","NEWT:118503","NEWT:2059687","NEWT:160488","NEWT:28104","NEWT:207559","NEWT:407821","NCBITaxon:2","NEWT:85057","NEWT:985076","NEWT:568708","NEWT:1215323","NEWT:986","NEWT:52641","NEWT:7159","NEWT:267671","NEWT:28532","NEWT:353152","NEWT:8496","NEWT:7165","NEWT:27448","NEWT:40674","NEWT:1194669","NEWT:51329","NEWT:243230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