Plectin-mediated cytoskeletal crosstalk controls cell tension and cohesion in epithelial sheets.
Actins
/ metabolism
Animals
Biomechanical Phenomena
Cytoskeleton
/ metabolism
Desmosomes
/ metabolism
Dogs
Epithelial Cells
/ metabolism
Gene Knockout Techniques
Humans
Keratins
/ metabolism
MCF-7 Cells
Madin Darby Canine Kidney Cells
Mice
Plectin
/ metabolism
Protein Isoforms
/ metabolism
Tensile Strength
Journal
The Journal of cell biology
ISSN: 1540-8140
Titre abrégé: J Cell Biol
Pays: United States
ID NLM: 0375356
Informations de publication
Date de publication:
09 02 2022
09 02 2022
Historique:
received:
25
05
2021
revised:
07
12
2021
accepted:
20
12
2021
entrez:
9
2
2022
pubmed:
10
2
2022
medline:
25
2
2022
Statut:
ppublish
Résumé
The coordinated interplay of cytoskeletal networks critically determines tissue biomechanics and structural integrity. Here, we show that plectin, a major intermediate filament-based cytolinker protein, orchestrates cortical cytoskeletal networks in epithelial sheets to support intercellular junctions. By combining CRISPR/Cas9-based gene editing and pharmacological inhibition, we demonstrate that in an F-actin-dependent context, plectin is essential for the formation of the circumferential keratin rim, organization of radial keratin spokes, and desmosomal patterning. In the absence of plectin-mediated cytoskeletal cross-linking, the aberrant keratin-desmosome (DSM)-network feeds back to the actin cytoskeleton, which results in elevated actomyosin contractility. Also, by complementing a predictive mechanical model with Förster resonance energy transfer-based tension sensors, we provide evidence that in the absence of cytoskeletal cross-linking, major intercellular junctions (adherens junctions and DSMs) are under intrinsically generated tensile stress. Defective cytoarchitecture and tensional disequilibrium result in reduced intercellular cohesion, associated with general destabilization of plectin-deficient sheets upon mechanical stress.
Identifiants
pubmed: 35139142
pii: 212995
doi: 10.1083/jcb.202105146
pmc: PMC8932528
pii:
doi:
Substances chimiques
Actins
0
Plectin
0
Protein Isoforms
0
Keratins
68238-35-7
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2022 Prechova et al.
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