Skin epithelial cells change their mechanics and proliferation upon snail-mediated EMT signalling
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
Skin cancer is the most commonly occurring cancer in the USA and Germany, and the fourth most common cancer worldwide. Snail-dependent epithelial-mesenchymal transition (EMT) was shown to initiate and promote skin cancer. Previous studies could show that EMT changes actin cortex regulation and cellular mechanics in epithelial cells of diverse tissue origin. However, in spite of its potentially high significance in the context of skin cancer, the effect of EMT on cellular mechanics, mitotic rounding and proliferation has not been studied in skin epithelial cells so far. In this work, we show that TGF-β-induced partial EMT results in a transformation of the mechanical phenotype of skin epithelial cells in a cell-cycle dependent manner. Concomitantly, we looked at EMT-induced changes of cell proliferation. While EMT decreases proliferation in 2D culture, we observed an EMT-induced boost of cellular proliferation when culturing cells as mechanically confined aggregates of skin epithelial cells. This proliferation boost was accompanied by enhanced mitotic rounding and composition changes of the actin cortex. We give evidence that observed EMT-induced changes depend on the EMT-upregulated transcription factor snail. Overall, our findings indicate that EMT-induced changes of cellular mechanics might play a currently unappreciated role in EMT-induced promotion of skin tumor proliferation.
Details
Original language | English |
---|---|
Pages (from-to) | 2585-2596 |
Number of pages | 12 |
Journal | Soft matter |
Volume | 18 |
Issue number | 13 |
Publication status | Published - 30 Mar 2022 |
Peer-reviewed | Yes |
External IDs
Scopus | 85127544937 |
---|---|
ORCID | /0000-0002-2433-916X/work/142250426 |
ORCID | /0000-0003-0189-3448/work/159607174 |
Keywords
Sustainable Development Goals
Keywords
- Cadherins/genetics, Cell Proliferation, Epithelial Cells, Epithelial-Mesenchymal Transition/genetics, Signal Transduction