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Journal ArticleDOI

Degrading devices: invadosomes in proteolytic cell invasion.

Stefan Linder, +2 more
- 10 Oct 2011 - 
- Vol. 27, Iss: 1, pp 185-211
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TLDR
An overview of the field is provided, with special focus on current developments such as intracellular transport processes, ultrastructural analysis, the possible involvement of invadosomes in disease, and the tentative identification of invadoomes in 3D environments and in vivo.
Abstract
Podosomes and invadopodia, collectively known as invadosomes, are cell-matrix contacts in a variety of cell types, such as monocytic cells or cancer cells, that have to cross tissue barriers. Both structures share an actin-rich core, which distinguishes them from other matrix contacts, and are regulated by a multitude of signaling pathways including RhoGTPases, kinases, actin-associated proteins, and microtubule-dependent transport. Invadosomes recruit and secrete proteinases and are thus able to lyse extracellular matrix components. They are therefore considered to be potential key structures in proteolytic cell invasion in both physiological and pathological settings. This review provides an overview of the field, with special focus on current developments such as intracellular transport processes, ultrastructural analysis, the possible involvement of invadosomes in disease, and the tentative identification of invadosomes in 3D environments and in vivo.

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Citations
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Role of Extracellular Matrix in Development and Cancer Progression.

TL;DR: The ways in which biophysical forces of the microenvironment influence biochemical regulation and cell phenotype during key stages of human development and cancer progression are reviewed.
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At the leading edge of three-dimensional cell migration.

TL;DR: It is proposed that the mode of 3D cell migration is governed by a signaling axis involving cell–matrix adhesions, RhoA signaling and actomyosin contractility, and that this might represent a universal mechanism that controls 3Dcell migration.
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Integrin traffic – the update

TL;DR: The initial concept of integrin traffic as a means to translocate adhesion receptors within the cell has now been expanded with the growing appreciation that traffic is intimately linked to the cell signalling apparatus.
References
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Journal ArticleDOI

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TL;DR: Cancer cells possess a broad spectrum of migration and invasion mechanisms and learning more about the cellular and molecular basis of these different migration/invasion programmes will help to understand how cancer cells disseminate and lead to new treatment strategies.
Journal ArticleDOI

The Extracellular Matrix: Not Just Pretty Fibrils

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Molecular complexity and dynamics of cell-matrix adhesions

TL;DR: Integrin-mediated adhesions can undergo dynamic changes in structure and molecular properties from dot-like focal complexes to stress-fiber-associated focal contacts, which can further 'mature' to form fibronectin-bound fibrillar adhesion.
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The ADAMs family of metalloproteases: multidomain proteins with multiple functions

TL;DR: This review will first discuss the properties of each of the domains of the ADAMs, then describe the involvement ofADAMs in selected biological processes, and highlight recent interesting findings suggesting roles for ADams in human disease.
Journal ArticleDOI

Microtubule acetylation promotes kinesin-1 binding and transport

TL;DR: It is shown that the kinesin-1 cargo protein JNK-interacting protein 1 (JIP1) is localized to only a subset of neurites in cultured neuronal cells, and microtubule PTMs are important markers of distinct microtubules populations and that they act to control motor-protein trafficking.
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