bioRxivBioengineeringPreprint
Organoid co-culture model of the cycling human endometrium in a fully-defined syntheticextracellular matrix reveals epithelial-stromal crosstalk
J. S. Gnecco, A. T. Brown, K. Buttrey, C. S. Ives, B. A. Goods, L. Baugh, V. Hernandez-Gordillo, M. Loring, K. Isaacson, L. G. Griffith
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
- organism: human
- assay: organoid / primary culture
- research focus: cell type annotation
- research focus: cell-cell communication
- approach: experimental assay
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