Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Fibrotic Substrate Stiffness Enhances Endometriotic Epithelial Cell Motility.

Created on 10 Sep 2026

Authors

Shohini Banerjee, Nane Manukyan, Kimberly M Stroka

Published in

Tissue engineering. Part A. Pages 19373341261486719. Sep 10, 2026. Epub Sep 10, 2026.

Abstract

Fibrosis is a common pathological feature of inflammatory conditions across various organ systems, leading to a marked increase in matrix stiffness. The effects of substrate stiffness on benign epithelial cells in fibrotic microenvironments remain less well characterized compared with malignant cell types. We used an endometriotic epithelial cell line and polyacrylamide hydrogels with tunable stiffness to model mechanically driven single-cell and multicellular migration. We identified a biphasic relationship between substrate stiffness and epithelial migration, where substrates of intermediate stiffness best promoted cell speed, actin stress fiber formation, focal adhesion presentation, and spheroid expansion compared with the soft and very stiff gel substrates. Increasing cellular contractility on the soft substrate and decreasing contractility on the fibrotic stiffness substrate led to an increase and decrease in cell speed, respectively. These findings suggest a role for how fibrosis as a biomechanical state regulates epithelial cell migration during the pathogenesis of benign yet invasive conditions.

PMID:
42720355
Bibliographic data and abstract were imported from PubMed on 10 Sep 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 10
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement