Scar matrix drives Piezo1 mediated stromal inflammation leading to placenta accreta spectrum

Nat Commun. 2024 Sep 27;15(1):8379. doi: 10.1038/s41467-024-52351-0.

Abstract

Scar tissue formation is a hallmark of wound repair in adults and can chronically affect tissue architecture and function. To understand the general phenomena, we sought to explore scar-driven imbalance in tissue homeostasis caused by a common, and standardized surgical procedure, the uterine scar due to cesarean surgery. Deep uterine scar is associated with a rapidly increasing condition in pregnant women, placenta accreta spectrum (PAS), characterized by aggressive trophoblast invasion into the uterus, frequently necessitating hysterectomy at parturition. We created a model of uterine scar, recapitulating PAS-like invasive phenotype, showing that scar matrix activates mechanosensitive ion channel, Piezo1, through glycolysis-fueled cellular contraction. Piezo1 activation increases intracellular calcium activity and Protein kinase C activation, leading to NF-κB nuclear translocation, and MafG stabilization. This inflammatory transformation of decidua leads to production of IL-8 and G-CSF, chemotactically recruiting invading trophoblasts towards scar, initiating PAS. Our study demonstrates aberrant mechanics of scar disturbs stroma-epithelia homeostasis in placentation, with implications in cancer dissemination.

MeSH terms

  • Animals
  • Cesarean Section / adverse effects
  • Cicatrix* / metabolism
  • Cicatrix* / pathology
  • Decidua / metabolism
  • Decidua / pathology
  • Female
  • Humans
  • Inflammation* / metabolism
  • Inflammation* / pathology
  • Interleukin-8 / metabolism
  • Ion Channels* / genetics
  • Ion Channels* / metabolism
  • Mice
  • NF-kappa B / metabolism
  • Placenta Accreta* / metabolism
  • Placenta Accreta* / pathology
  • Pregnancy
  • Protein Kinase C / genetics
  • Protein Kinase C / metabolism
  • Trophoblasts* / metabolism
  • Trophoblasts* / pathology
  • Uterus / metabolism
  • Uterus / pathology

Substances

  • Ion Channels
  • PIEZO1 protein, human
  • NF-kappa B
  • Protein Kinase C
  • Interleukin-8