Unknown

Dataset Information

0

Metavinculin modulates force transduction in cell adhesion sites.


ABSTRACT: Vinculin is a ubiquitously expressed protein, crucial for the regulation of force transduction in cells. Muscle cells express a vinculin splice-isoform called metavinculin, which has been associated with cardiomyopathies. However, the molecular function of metavinculin has remained unclear and its role for heart muscle disorders undefined. Here, we have employed a set of piconewton-sensitive tension sensors to probe metavinculin mechanics in cells. Our experiments reveal that metavinculin bears higher molecular forces but is less frequently engaged as compared to vinculin, leading to altered force propagation in cell adhesions. In addition, we have generated knockout mice to investigate the consequences of metavinculin loss in vivo. Unexpectedly, these animals display an unaltered tissue response in a cardiac hypertrophy model. Together, the data reveal that the transduction of cell adhesion forces is modulated by expression of metavinculin, yet its role for heart muscle function seems more subtle than previously thought.

SUBMITTER: Kanoldt V 

PROVIDER: S-EPMC7747745 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications


Vinculin is a ubiquitously expressed protein, crucial for the regulation of force transduction in cells. Muscle cells express a vinculin splice-isoform called metavinculin, which has been associated with cardiomyopathies. However, the molecular function of metavinculin has remained unclear and its role for heart muscle disorders undefined. Here, we have employed a set of piconewton-sensitive tension sensors to probe metavinculin mechanics in cells. Our experiments reveal that metavinculin bears  ...[more]

Similar Datasets

| S-EPMC4803541 | biostudies-literature
| S-EPMC6726196 | biostudies-literature
| S-EPMC3556026 | biostudies-literature
| S-EPMC6053543 | biostudies-literature
| S-EPMC7091509 | biostudies-literature
| S-EPMC3192957 | biostudies-literature
| S-EPMC2898422 | biostudies-literature
| S-EPMC7173973 | biostudies-literature
| S-EPMC2675629 | biostudies-literature
| S-EPMC10103301 | biostudies-literature