Extracellular Matrix Composition and Stiffness Regulates Progesterone Responsiveness and Decidualization

Danielle Klunk, Laura Homewood, Daniel Abebayehu
In: iScience · 2026 · vol. 29(9) , pp. 117009 · doi:10.1016/j.isci.2026.117009 · W7168251937
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This study demonstrates that extracellular matrix stiffness and composition modulate progesterone-induced decidualization in fibroblasts, with stiff matrices and fibronectin inhibiting differentiation, mirroring findings in endometriosis lesions.

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Abstract

Endometriosis is an inflammatory disease of endometrium found outside the uterus. Approximately a third of patients remain unresponsive to hormonal treatments due to progesterone resistance. Because endometriosis lesions are found within fibrotic extracellular matrix (ECM), we hypothesized that ECM stiffness and composition regulate progesterone responses. We used hydrogels to mimic physiological stiffnesses and examine how mechanical and biochemical ECM cues influence progesterone-induced differentiation (decidualization) in healthy fibroblasts. We determined that ECM ligands modulate decidualization, with laminin slowing secretory responses in favor of stabilizing upstream FOXO1 and WNT4 signaling, while fibronectin produces quicker but less stabilized differentiation. Stiff matrices override these ECM cues and inhibit decidualization across ligands. Furthermore, these findings mirror activity in endometriotic lesions based on lesions across stiffest sites displaying greater fibronectin expression and lower decidualization. Altogether, these data demonstrate a role for lesion microenvironment in the mechanism of inhibited decidualization and progesterone responses.

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