Abstract
Podosomes are dynamic actin-based membrane protrusions that are important for extracellular matrix degradation and invasive cell motility. Individual podosomes are often found to organize into large rosette-like structures in some types of cells, such as osteoclasts, endothelial cells, Src-transformed fibroblasts, and certain highly invasive cancer cells. In this study, we show that new podosome rosettes arise through one of two mechanisms; de novo assembly or fission of a pre-existing podosome rosette in Src-transformed fibroblasts. Fission is a more efficient way than de novo assembly to generate new podosome rosettes in these cells. Podosome rosettes undergoing fission possess higher motility and a stronger matrix-degrading capability. Podosome rosette fission may be the result of polarized myosin II-mediated contractility of these structures, which is coordinately regulated by myosin light chain kinase and Rho-associated kinase II. Collectively, this study unveils a previously unknown mechanism - fission for the biogenesis of podosome rosettes.
| Original language | English |
|---|---|
| Article number | 524 |
| Journal | Scientific reports |
| Volume | 8 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2018 Dec 1 |
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All Science Journal Classification (ASJC) codes
- General
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Biogenesis of podosome rosettes through fission. / Kuo, Szu Lin; Chen, Chien Lin; Pan, Yi Ru; Chiu, Wen Tai; Chen, Hong Chen.
In: Scientific reports, Vol. 8, No. 1, 524, 01.12.2018.Research output: Contribution to journal › Article
TY - JOUR
T1 - Biogenesis of podosome rosettes through fission
AU - Kuo, Szu Lin
AU - Chen, Chien Lin
AU - Pan, Yi Ru
AU - Chiu, Wen Tai
AU - Chen, Hong Chen
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Podosomes are dynamic actin-based membrane protrusions that are important for extracellular matrix degradation and invasive cell motility. Individual podosomes are often found to organize into large rosette-like structures in some types of cells, such as osteoclasts, endothelial cells, Src-transformed fibroblasts, and certain highly invasive cancer cells. In this study, we show that new podosome rosettes arise through one of two mechanisms; de novo assembly or fission of a pre-existing podosome rosette in Src-transformed fibroblasts. Fission is a more efficient way than de novo assembly to generate new podosome rosettes in these cells. Podosome rosettes undergoing fission possess higher motility and a stronger matrix-degrading capability. Podosome rosette fission may be the result of polarized myosin II-mediated contractility of these structures, which is coordinately regulated by myosin light chain kinase and Rho-associated kinase II. Collectively, this study unveils a previously unknown mechanism - fission for the biogenesis of podosome rosettes.
AB - Podosomes are dynamic actin-based membrane protrusions that are important for extracellular matrix degradation and invasive cell motility. Individual podosomes are often found to organize into large rosette-like structures in some types of cells, such as osteoclasts, endothelial cells, Src-transformed fibroblasts, and certain highly invasive cancer cells. In this study, we show that new podosome rosettes arise through one of two mechanisms; de novo assembly or fission of a pre-existing podosome rosette in Src-transformed fibroblasts. Fission is a more efficient way than de novo assembly to generate new podosome rosettes in these cells. Podosome rosettes undergoing fission possess higher motility and a stronger matrix-degrading capability. Podosome rosette fission may be the result of polarized myosin II-mediated contractility of these structures, which is coordinately regulated by myosin light chain kinase and Rho-associated kinase II. Collectively, this study unveils a previously unknown mechanism - fission for the biogenesis of podosome rosettes.
UR - http://www.scopus.com/inward/record.url?scp=85040465101&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85040465101&partnerID=8YFLogxK
U2 - 10.1038/s41598-017-18861-2
DO - 10.1038/s41598-017-18861-2
M3 - Article
C2 - 29323185
AN - SCOPUS:85040465101
VL - 8
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
IS - 1
M1 - 524
ER -