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The matrix corroded

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The matrix corroded : podosomes and invadopodia in extracellular matrix degradation. / Linder, Stefan.

In: TRENDS CELL BIOL, Vol. 17, No. 3, 01.03.2007, p. 107-17.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Linder, S 2007, 'The matrix corroded: podosomes and invadopodia in extracellular matrix degradation', TRENDS CELL BIOL, vol. 17, no. 3, pp. 107-17. https://doi.org/10.1016/j.tcb.2007.01.002

APA

Linder, S. (2007). The matrix corroded: podosomes and invadopodia in extracellular matrix degradation. TRENDS CELL BIOL, 17(3), 107-17. https://doi.org/10.1016/j.tcb.2007.01.002

Vancouver

Linder S. The matrix corroded: podosomes and invadopodia in extracellular matrix degradation. TRENDS CELL BIOL. 2007 Mar 1;17(3):107-17. https://doi.org/10.1016/j.tcb.2007.01.002

Bibtex

@article{97333f2c9d2a490babd0b7bdacacafc6,
title = "The matrix corroded: podosomes and invadopodia in extracellular matrix degradation",
abstract = "Podosomes and invadopodia are unique actin-rich adhesions that establish close contact to the substratum but can also degrade components of the extracellular matrix. Accordingly, matrix degradation localized at podosomes or invadopodia is thought to contribute to cellular invasiveness in physiological and pathological situations. Cell types that form podosomes include monocytic, endothelial and smooth muscle cells, whereas invadopodia have been mostly observed in carcinoma cells. This review highlights important new developments in the field, discusses the common and divergent features of podosomes and invadopodia and summarizes current knowledge about matrix-degrading proteinases at these structures.",
keywords = "Animals, Cell Adhesion, Cell Surface Extensions, Cytoskeleton, Extracellular Matrix, Humans, Peptide Hydrolases, Signal Transduction",
author = "Stefan Linder",
year = "2007",
month = mar,
day = "1",
doi = "10.1016/j.tcb.2007.01.002",
language = "English",
volume = "17",
pages = "107--17",
journal = "TRENDS CELL BIOL",
issn = "0962-8924",
publisher = "Elsevier Limited",
number = "3",

}

RIS

TY - JOUR

T1 - The matrix corroded

T2 - podosomes and invadopodia in extracellular matrix degradation

AU - Linder, Stefan

PY - 2007/3/1

Y1 - 2007/3/1

N2 - Podosomes and invadopodia are unique actin-rich adhesions that establish close contact to the substratum but can also degrade components of the extracellular matrix. Accordingly, matrix degradation localized at podosomes or invadopodia is thought to contribute to cellular invasiveness in physiological and pathological situations. Cell types that form podosomes include monocytic, endothelial and smooth muscle cells, whereas invadopodia have been mostly observed in carcinoma cells. This review highlights important new developments in the field, discusses the common and divergent features of podosomes and invadopodia and summarizes current knowledge about matrix-degrading proteinases at these structures.

AB - Podosomes and invadopodia are unique actin-rich adhesions that establish close contact to the substratum but can also degrade components of the extracellular matrix. Accordingly, matrix degradation localized at podosomes or invadopodia is thought to contribute to cellular invasiveness in physiological and pathological situations. Cell types that form podosomes include monocytic, endothelial and smooth muscle cells, whereas invadopodia have been mostly observed in carcinoma cells. This review highlights important new developments in the field, discusses the common and divergent features of podosomes and invadopodia and summarizes current knowledge about matrix-degrading proteinases at these structures.

KW - Animals

KW - Cell Adhesion

KW - Cell Surface Extensions

KW - Cytoskeleton

KW - Extracellular Matrix

KW - Humans

KW - Peptide Hydrolases

KW - Signal Transduction

U2 - 10.1016/j.tcb.2007.01.002

DO - 10.1016/j.tcb.2007.01.002

M3 - SCORING: Journal article

C2 - 17275303

VL - 17

SP - 107

EP - 117

JO - TRENDS CELL BIOL

JF - TRENDS CELL BIOL

SN - 0962-8924

IS - 3

ER -