| Literature DB >> 33767161 |
K Venkatesan Iyer1,2,3, Anna Taubenberger4, Salma Ahmed Zeidan5, Natalie A Dye5,6, Suzanne Eaton5,6, Frank Jülicher7,8,9.
Abstract
The levels of nuclear protein Lamin A/C are crucial for nuclear mechanotransduction. Lamin A/C levels are known to scale with tissue stiffness and extracellular matrix levels in mesenchymal tissues. But in epithelial tissues, where cells lack a strong interaction with the extracellular matrix, it is unclear how Lamin A/C is regulated. Here, we show in epithelial tissues that Lamin A/C levels scale with apico-basal cell compression, independent of tissue stiffness. Using genetic perturbations in Drosophila epithelial tissues, we show that apico-basal cell compression regulates the levels of Lamin A/C by deforming the nucleus. Further, in mammalian epithelial cells, we show that nuclear deformation regulates Lamin A/C levels by modulating the levels of phosphorylation of Lamin A/C at Serine 22, a target for Lamin A/C degradation. Taken together, our results reveal a mechanism of Lamin A/C regulation which could provide key insights for understanding nuclear mechanotransduction in epithelial tissues.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33767161 DOI: 10.1038/s41467-021-22010-9
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919