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Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages
Podosomes, an important actin-based adhesive architecture, play critical roles in cell migration and matrix invasiveness. Here, we elucidate the ultrastructural organization and regulation of podosome clusters in primary macrophages. With three-dimensional stochastic optical reconstruction microscop...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678738/ https://www.ncbi.nlm.nih.gov/pubmed/36425766 http://dx.doi.org/10.1016/j.isci.2022.105514 |
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author | Hu, Fen Zhu, Donglan Dong, Hao Zhang, Ping Xing, Fulin Li, Wan Yan, Rui Zhou, Jun Xu, Ke Pan, Leiting Xu, Jingjun |
author_facet | Hu, Fen Zhu, Donglan Dong, Hao Zhang, Ping Xing, Fulin Li, Wan Yan, Rui Zhou, Jun Xu, Ke Pan, Leiting Xu, Jingjun |
author_sort | Hu, Fen |
collection | PubMed |
description | Podosomes, an important actin-based adhesive architecture, play critical roles in cell migration and matrix invasiveness. Here, we elucidate the ultrastructural organization and regulation of podosome clusters in primary macrophages. With three-dimensional stochastic optical reconstruction microscopy (3D-STORM), we achieve ∼20/50 nm (lateral/axial) spatial resolution to resolve the mutual localization of podosome core and ring components, and further show that microtubules pass through podosomes at the layer of myosin IIA. The microtubule disruption-caused podosome dissolution is previously ascribed to Rho/ROCK-myosin signaling, yet inhibiting this pathway with Y27632 or blebbistatin only partially recovers podosome assembly, thus suggesting the contribution of the physical supporting of microtubules in stabilizing podosome structures. Through improved substrate-coating technique, we further corroborate that the matrix-degrading capability of macrophages depends on the formation of podosome clusters. Together, 3D-STORM super-resolution microscopy reveals the nanoscale spatial arrangement and the microtubule-dependent regulation of the matrix-degrading podosome clusters in macrophages. |
format | Online Article Text |
id | pubmed-9678738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96787382022-11-23 Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages Hu, Fen Zhu, Donglan Dong, Hao Zhang, Ping Xing, Fulin Li, Wan Yan, Rui Zhou, Jun Xu, Ke Pan, Leiting Xu, Jingjun iScience Article Podosomes, an important actin-based adhesive architecture, play critical roles in cell migration and matrix invasiveness. Here, we elucidate the ultrastructural organization and regulation of podosome clusters in primary macrophages. With three-dimensional stochastic optical reconstruction microscopy (3D-STORM), we achieve ∼20/50 nm (lateral/axial) spatial resolution to resolve the mutual localization of podosome core and ring components, and further show that microtubules pass through podosomes at the layer of myosin IIA. The microtubule disruption-caused podosome dissolution is previously ascribed to Rho/ROCK-myosin signaling, yet inhibiting this pathway with Y27632 or blebbistatin only partially recovers podosome assembly, thus suggesting the contribution of the physical supporting of microtubules in stabilizing podosome structures. Through improved substrate-coating technique, we further corroborate that the matrix-degrading capability of macrophages depends on the formation of podosome clusters. Together, 3D-STORM super-resolution microscopy reveals the nanoscale spatial arrangement and the microtubule-dependent regulation of the matrix-degrading podosome clusters in macrophages. Elsevier 2022-11-05 /pmc/articles/PMC9678738/ /pubmed/36425766 http://dx.doi.org/10.1016/j.isci.2022.105514 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Hu, Fen Zhu, Donglan Dong, Hao Zhang, Ping Xing, Fulin Li, Wan Yan, Rui Zhou, Jun Xu, Ke Pan, Leiting Xu, Jingjun Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title | Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title_full | Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title_fullStr | Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title_full_unstemmed | Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title_short | Super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
title_sort | super-resolution microscopy reveals nanoscale architecture and regulation of podosome clusters in primary macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678738/ https://www.ncbi.nlm.nih.gov/pubmed/36425766 http://dx.doi.org/10.1016/j.isci.2022.105514 |
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