The fallopian tubes are essential to several physiological and pathological processes from pregnancy to ovarian cancer. However, current in vitro models to study their pathophysiology were validated using two-dimensional (2D) tissue sections and measuring the organoid response to female hormone stimulation. These analyses overlook the 3D heterogeneity of the tissue and the fallopian tube mechanical function (transport of an oocyte). We developed a multi-compartment organoid model of the human fallopian tube that was meticulously tuned to reflect the compartmentalization and heterogeneity of the tissue composition. We validated the proteome, cilia-driven transport function, and architectural accuracy of this organoid through a novel platform wherein organoids are quantitatively compared to a 3D single-cell resolution reference map of a healthy, transplantation-quality human fallopian tube. This organoid model was precision-engineered using our iterative platform to resemble the cellular and extracellular proteome, biological function, and 3D microanatomy of the human fallopian tube.
[doi:10.25345/C5028PQ1D]
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Human fallopian tube ; Organoid ; Quantitative proteomics ; diaPASEF ; Data-independent acquisition (DIA)
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Birgit Schilling, Buck Institute, USA |
Submitting User: | JoannaBons |
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Owner | Reanalyses | |
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