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Biomechanical regulation of focal adhesion and invadopodia formation
- Source :
- Journal of Cell Science. 133
- Publication Year :
- 2020
- Publisher :
- The Company of Biologists, 2020.
-
Abstract
- Integrin adhesions are a structurally and functionally diverse family of transmembrane, multi-protein complexes that link the intracellular cytoskeleton to the extracellular matrix (ECM). The different members of this family, including focal adhesions (FAs), focal complexes, fibrillar adhesions, podosomes and invadopodia, contain many shared scaffolding and signaling ‘adhesome’ components, as well as distinct molecules that perform specific functions, unique to each adhesion form. In this Hypothesis, we address the pivotal roles of mechanical forces, generated by local actin polymerization or actomyosin-based contractility, in the formation, maturation and functionality of two members of the integrin adhesions family, namely FAs and invadopodia, which display distinct structures and functional properties. FAs are robust and stable ECM contacts, associated with contractile stress fibers, while invadopodia are invasive adhesions that degrade the underlying matrix and penetrate into it. We discuss here the mechanisms, whereby these two types of adhesion utilize a similar molecular machinery to drive very different – often opposing cellular activities, and hypothesize that early stages of FAs and invadopodia assembly use similar biomechanical principles, whereas maturation of the two structures, and their ‘adhesive’ and ‘invasive’ functionalities require distinct sources of biomechanical reinforcement.
- Subjects :
- Focal Adhesions
Integrins
0303 health sciences
biology
Podosome
Adhesome
Integrin
Cell Biology
Extracellular Matrix
Cell biology
Focal adhesion
Extracellular matrix
03 medical and health sciences
0302 clinical medicine
Podosomes
Invadopodia
Cell Adhesion
biology.protein
Cell adhesion
Cytoskeleton
030217 neurology & neurosurgery
030304 developmental biology
Subjects
Details
- ISSN :
- 14779137 and 00219533
- Volume :
- 133
- Database :
- OpenAIRE
- Journal :
- Journal of Cell Science
- Accession number :
- edsair.doi.dedup.....ac01d62ea80b6e8f2ea10ea8347745ea
- Full Text :
- https://doi.org/10.1242/jcs.244848