Proteomics

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Remodeling of the focal adhesion complex by hydrogen-peroxide- induced senescence


ABSTRACT: Cellular senescence is a phenotype characterized by cessation of cell division, which can be caused by exhaustive replication or environmental stress. It is involved in age-related pathophysiological conditions and affects both the cellular cytoskeleton and the prime cellular mechanosensors, focal adhesion complexes. While the size of focal adhesions increases during senescence, it is unknown if and how this is accompanied by a remodeling of the internal focal adhesion structure. Our study uses metal-induced energy transfer to study the axial dimension of focal adhesion proteins from oxidative-stress-induced senescent cells with nanometer precision, and compares these to unstressed cells. We influenced cytoskeletal tension and the functioning of mechanosensitive ion channels using drugs and studied the combined effect of senescence and drug intervention on the focal adhesion structure. We find that H 2 O 2 induced restructuring of the focal adhesion complex indicates a loss of tension and altered talin complexation. Mass spectroscopy-based proteomics confirmed the differential regulation of several cytoskeletal proteins induced by H 2 O 2 treatment.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Cell Culture, Fibroblast

SUBMITTER: Meytal Radzinski  

LAB HEAD: Kay-Eberhard Gottschalk

PROVIDER: PXD041766 | Pride | 2023-07-06

REPOSITORIES: Pride

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Publications

Remodeling of the focal adhesion complex by hydrogen-peroxide-induced senescence.

Grandy Carolin C   Port Fabian F   Radzinski Meytal M   Singh Karmveer K   Erz Dorothee D   Pfeil Jonas J   Reichmann Dana D   Gottschalk Kay-Eberhard KE  

Scientific reports 20230615 1


Cellular senescence is a phenotype characterized by cessation of cell division, which can be caused by exhaustive replication or environmental stress. It is involved in age-related pathophysiological conditions and affects both the cellular cytoskeleton and the prime cellular mechanosensors, focal adhesion complexes. While the size of focal adhesions increases during senescence, it is unknown if and how this is accompanied by a remodeling of the internal focal adhesion structure. Our study uses  ...[more]

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