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bioRxiv · 10.1101/2021.09.30.462577

Tissue engineered organoid co-culture model of the cycling human endometrium in a fully-defined synthetic extracellular matrix

Gnecco, J. S.·Brown, A. T.·Buttrey, K.·Ives, C. S.·Goods, B. A.·Baugh, L.·Hernandez-Gordillo, V.·Loring, M.·Isaacson, K.·Griffith, L. G.
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Abstract

The human endometrium undergoes recurring cycles of growth, differentiation, and breakdown in response to sex hormones. Dysregulation of epithelial-stromal communication during hormone cycles is linked to myriad gynecological disorders for which treatments remain inadequate. Here, we describe a completely defined, synthetic extracellular matrix that enables co-culture of human endometrial epithelial and stromal cells in a manner that captures healthy and disease states across a simulated menstrual cycle. We parsed cycle-dependent endometrial integrin expression and matrix composition to define candidate cell-matrix interaction cues for inclusion in a polyethylene glycol (PEG)-based hydrogel crosslinked with matrix metalloproteinase-labile peptides. We semi-empirically screened a parameter space of biophysical and molecular features representative of the endometrium to define compositions suitable for hormone-driven expansion and differentiation of epithelial organoids, stromal cells, and co-cultures of the two cell types. Each cell type exhibited characteristic morphological and molecular responses to hormone changes when co-encapsulated in hydrogels tuned to a stiffness regime similar to the native tissue and functionalized with a collagen-derived adhesion peptide (GFOGER) and a fibronectin-derived peptide (PHSRN-K-RGD). Analysis of cell-cell crosstalk during IL-1{beta}-induced inflammation revealed dysregulation of epithelial proliferation mediated by stromal cells. Altogether, we demonstrate the development of a fully synthetic matrix to sustain the dynamic changes of the endometrial microenvironment and support its applications to understand menstrual health and endometriotic diseases. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=114 SRC="FIGDIR/small/462577v2_ufig1.gif" ALT="Figure 1"> View larger version (47K): org.highwire.dtl.DTLVardef@1cc97dcorg.highwire.dtl.DTLVardef@1061157org.highwire.dtl.DTLVardef@15c8c35org.highwire.dtl.DTLVardef@f902d7_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Gnecco, J. S., Brown, A. T., Buttrey, K., Ives, C. S., Goods, B. A., Baugh, L., Hernandez-Gordillo, V., Loring, M., Isaacson, K., Griffith, L. G.. 2021-10-01. Tissue engineered organoid co-culture model of the cycling human endometrium in a fully-defined synthetic extracellular matrix. https://doi.org/10.1101/2021.09.30.462577

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