Mechanosensitive channel PIEZO1 enhances endometrial decidualization via BECN1-dependent autophagy

Kang, J.-W.; Wu, Y.; Zhang, Y.; Li, H.-X.; Li, G.-Y.; Yang, Y.-F.; Huang, X.-Q.; Yu, J.-Y.; Liang, C.; Zhang, R.; Liu, X.-Z.; Song, S.-S.; Liu, Y.-N.; Shaukat, A.; Song, Y.; Hrbek, S.; Lydon, J. P.; Guo, B.; Diao, H.-L.; Yang, Z.-M.; Fazleabas, A.; Su, R.-W.

doi:10.1101/2025.08.05.668790

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bioRxiv · 10.1101/2025.08.05.668790

Mechanosensitive channel PIEZO1 enhances endometrial decidualization via BECN1-dependent autophagy

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Abstract

The mechanosensitive ion channel PIEZO1 plays critical roles in physiological and pathological processes in response to various types of mechanical forces, including shear stress, stretch, and extracellular matrix (ECM) stiffness. Decidualization is crucial for a successful pregnancy, characterized by the differentiation of fibroblastic endometrial stromal cells into round, secretory decidual cells, along with the rapid remodeling of the ECM. Herein, we report that PIEZO1 plays a crucial role in enhancing decidualization in response to extracellular matrix (ECM) stiffness and cell contraction. Uterine-specific knockout of Piezo1 using Pgr-Cre in mice results in subfertility due to decidualization impairment in mid-late pregnancy. Silencing of PIEZO1 in human endometrial stromal cells also results in impaired decidualization. Treatment with the PIEZO1 agonist Yoda1 enhances decidualization in both in vivo and in vitro models. Stromal cells growing on ECM with 25 kPa stiffness display a better decidualization response than cells seeded on softer 2 kPa surface or harder surface of the regulator petri dish, and this difference is abolished by null of Piezo1. Consistent with PIEZO1 as a Ca2+ modulator, blocking of intracellular Ca2+ or pCaMKII significantly inhibits Yoda1-enhanced decidualization. Further investigation reveals that BECN1-dependent autophagy acts as the downstream of PIEZO1. Silencing of Beclin1 abolishes Yoda1-induced decidualization, while Tat-BECN1 fully rescues impaired decidualization caused by the lack of PIEZO1. Finally, the lower expression of PIEZO1 is associated with impaired decidualization in the endometrium of endometriotic baboons. In conclusion, we have uncovered a novel mechanism of decidualization that is regulated by PIEZO1-mediated mechanotransduction, providing further insight into decidualization studies. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=187 HEIGHT=200 SRC="FIGDIR/small/668790v1_ufig1.gif" ALT="Figure 1"> View larger version (68K): org.highwire.dtl.DTLVardef@2d25faorg.highwire.dtl.DTLVardef@186e56org.highwire.dtl.DTLVardef@1f3f61borg.highwire.dtl.DTLVardef@1a26bb7_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Kang, J.-W., Wu, Y., Zhang, Y., Li, H.-X., Li, G.-Y., Yang, Y.-F., Huang, X.-Q., Yu, J.-Y., Liang, C., Zhang, R., Liu, X.-Z., Song, S.-S., Liu, Y.-N., Shaukat, A., Song, Y., Hrbek, S., Lydon, J. P., Guo, B., Diao, H.-L., Yang, Z.-M., Fazleabas, A., Su, R.-W.. 2025-08-07. Mechanosensitive channel PIEZO1 enhances endometrial decidualization via BECN1-dependent autophagy. https://doi.org/10.1101/2025.08.05.668790

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