Differential Talin cleavage in transformed and non-transformed cells and its consequences.

TIRF and FRAP calpain cancer biology focal adhesion mechanobiology talin cleavage

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2024
Historique:
received: 10 05 2024
accepted: 03 06 2024
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 1 8 2024
Statut: epublish

Résumé

This study investigates differences in focal adhesion (FA) morphology and Talin cleavage levels between transformed and non-transformed cell lines. Utilizing fluorescently tagged wild-type Talin and Talin mutants with calpain cleavage site mutations, FA structures were visualized. Mutations in different Talin cleavage sites showed varying impacts on FA morphology and distribution across melanoma cell lines (Meljuso, A375P, A2058) and a non-transformed cell line (HFF). Western blot analysis, ratiometric fluorescence intensity-based measurements, and FRAP experiments revealed higher Talin cleavage levels within FAs of transformed cell lines compared to non-transformed cells. Additionally, growth assays indicated that reducing calpain cleavage levels attenuated transformed cell growth. These findings suggest that Talin cleavage level is crucial for FA morphology and assembly, with higher levels observed in transformed cells, influencing their growth dynamics.

Identifiants

pubmed: 39086658
doi: 10.3389/fcell.2024.1430728
pii: 1430728
pmc: PMC11289324
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1430728

Informations de copyright

Copyright © 2024 Hu, Jalal, Yao, Bakke, Margadant and Sheetz.

Déclaration de conflit d'intérêts

Authors FM and MS are shareholders of Mechanobiologics. Inc. Authors FM, MY and MS hold patents in the field. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Xian Hu (X)

Center for Cancer Cell Reprogramming, Faculty of Medicine, University of Oslo, Oslo, Norway.
Department of Biosciences, University of Oslo, Oslo, Norway.

Salma Jalal (S)

Mechanobiology Institute, National University of Singapore, Singapore, Singapore.

Mingxi Yao (M)

Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, Guangdong, China.

Oddmund Bakke (O)

Department of Biosciences, University of Oslo, Oslo, Norway.

Felix Margadant (F)

Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
Molecular Mechanomedicine Program, Biochemistry and Molecular Biology Department, University of Texas Medical Branch, Galveston, TX, United States.

Michael Sheetz (M)

Mechanobiology Institute, National University of Singapore, Singapore, Singapore.
Molecular Mechanomedicine Program, Biochemistry and Molecular Biology Department, University of Texas Medical Branch, Galveston, TX, United States.

Classifications MeSH