Ulcerative colitis is a debilitating and recurrent condition with significant co-morbidities including risk of developing cancer and that is associated with extensive tissue remodeling that is both a consequence and mediator of disease progression. Here, label-free mass spectrometry was used to characterise extracellular matrix remodelling in a murine model of colitis. Unique proteomic profiles of the extracellular matrix landscape distinguished inflamed from matched-normal colon tissue thus identifying pre- and pathological colitic states that were predominantly differentiated by expression of proteoglycans. Network maps derived from this dataset highlighted a central role for matrisomal proteins in epithelial-stromal interactions and identified orchestrating nodes that could be exploited in selection of therapeutic targets.
[doi:10.25345/C5MW28Q9W]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Inflammatory Bowel Diseases ; Extracellular Matrix ; Proteoglycans ; Quantitative Proteomics ; Data-Independent Acquisition (DIA)
Principal Investigators: (in alphabetical order) |
Birgit Schilling, Buck Institute, USA |
Submitting User: | JoannaBons |
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