TY - JOUR
T1 - Mechanisms and roles of podosomes and invadopodia
AU - Linder, Stefan
AU - Cervero, Pasquale
AU - Eddy, Robert
AU - Condeelis, John
N1 - Funding Information:
S.L. and P.C. thank A. Mordhorst for expert technical assistance, the UKE Microscopy Imaging Facility for support with imaging and M. Aepfelbacher for continuous support. Work on podosomes and matrix metalloproteinases in the S.L. laboratory is supported by the Deutsche Forschungsgemeinschaft (LI925/8-1 and CRC877/B13), and work on invadopodia in the J.C. laboratory is supported by grants from the US National Cancer Institute (CA216248 and CA255153). The authors apologize to all authors whose work has not been mentioned due to space limitations.
Publisher Copyright:
© 2022, Springer Nature Limited.
PY - 2023/2
Y1 - 2023/2
N2 - Cell invasion into the surrounding extracellular matrix or across tissue boundaries and endothelial barriers occurs in both physiological and pathological scenarios such as immune surveillance or cancer metastasis. Podosomes and invadopodia, collectively called ‘invadosomes’, are actin-based structures that drive the proteolytic invasion of cells, by forming highly regulated platforms for the localized release of lytic enzymes that degrade the matrix. Recent advances in high-resolution microscopy techniques, in vivo imaging and high-throughput analyses have led to considerable progress in understanding mechanisms of invadosomes, revealing the intricate inner architecture of these structures, as well as their growing repertoire of functions that extends well beyond matrix degradation. In this Review, we discuss the known functions, architecture and regulatory mechanisms of podosomes and invadopodia. In particular, we describe the molecular mechanisms of localized actin turnover and microtubule-based cargo delivery, with a special focus on matrix-lytic enzymes that enable proteolytic invasion. Finally, we point out topics that should become important in the invadosome field in the future.
AB - Cell invasion into the surrounding extracellular matrix or across tissue boundaries and endothelial barriers occurs in both physiological and pathological scenarios such as immune surveillance or cancer metastasis. Podosomes and invadopodia, collectively called ‘invadosomes’, are actin-based structures that drive the proteolytic invasion of cells, by forming highly regulated platforms for the localized release of lytic enzymes that degrade the matrix. Recent advances in high-resolution microscopy techniques, in vivo imaging and high-throughput analyses have led to considerable progress in understanding mechanisms of invadosomes, revealing the intricate inner architecture of these structures, as well as their growing repertoire of functions that extends well beyond matrix degradation. In this Review, we discuss the known functions, architecture and regulatory mechanisms of podosomes and invadopodia. In particular, we describe the molecular mechanisms of localized actin turnover and microtubule-based cargo delivery, with a special focus on matrix-lytic enzymes that enable proteolytic invasion. Finally, we point out topics that should become important in the invadosome field in the future.
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U2 - 10.1038/s41580-022-00530-6
DO - 10.1038/s41580-022-00530-6
M3 - Review article
C2 - 36104625
AN - SCOPUS:85138070172
SN - 1471-0072
VL - 24
SP - 86
EP - 106
JO - Nature Reviews Molecular Cell Biology
JF - Nature Reviews Molecular Cell Biology
IS - 2
ER -