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Confined environments induce polarized paraspeckle condensates

Cancer cells experience confinement as they navigate the tumour microenvironment during metastasis. Recent studies have revealed that the nucleus can function as a ‘ruler’ for measuring physical confinement via membrane tension, allowing for compression-sensitive changes in migration. Cell nuclei co...

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Autores principales: Todorovski, Vanja, McCluggage, Finn, Li, Yixuan, Meid, Annika, Spatz, Joachim P., Holle, Andrew W., Fox, Archa H., Choi, Yu Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9898560/
https://www.ncbi.nlm.nih.gov/pubmed/36737664
http://dx.doi.org/10.1038/s42003-023-04528-4
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author Todorovski, Vanja
McCluggage, Finn
Li, Yixuan
Meid, Annika
Spatz, Joachim P.
Holle, Andrew W.
Fox, Archa H.
Choi, Yu Suk
author_facet Todorovski, Vanja
McCluggage, Finn
Li, Yixuan
Meid, Annika
Spatz, Joachim P.
Holle, Andrew W.
Fox, Archa H.
Choi, Yu Suk
author_sort Todorovski, Vanja
collection PubMed
description Cancer cells experience confinement as they navigate the tumour microenvironment during metastasis. Recent studies have revealed that the nucleus can function as a ‘ruler’ for measuring physical confinement via membrane tension, allowing for compression-sensitive changes in migration. Cell nuclei contain many nuclear bodies that form when their components phase separate and condense within permissive local regions within the nucleus. However, how sub-nuclear organisation and phase separation changes with cell confinement and compression is largely unknown. Here we focus on paraspeckles, stress-responsive subnuclear bodies that form by phase separation around the long non-coding RNA NEAT1. As cells entered moderate confinement, a significant increase in paraspeckle number and size was observed compared to unconfined cells. Paraspeckle polarization bias towards the leading edge was also observed in confinement, correlating with regions of euchromatin. Increasing paraspeckle abundance resulted in increases in confined migration likelihood, speed, and directionality, as well as an enhancement of paraspeckle polarization towards the leading edge. This polarization of paraspeckle condensates may play a key role in regulating confined migration and invasion in cancer cells, and illustrates the utility of microchannel-based assays for identifying phenomena not observed on 2D or 3D bulk substrates.
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spelling pubmed-98985602023-02-05 Confined environments induce polarized paraspeckle condensates Todorovski, Vanja McCluggage, Finn Li, Yixuan Meid, Annika Spatz, Joachim P. Holle, Andrew W. Fox, Archa H. Choi, Yu Suk Commun Biol Article Cancer cells experience confinement as they navigate the tumour microenvironment during metastasis. Recent studies have revealed that the nucleus can function as a ‘ruler’ for measuring physical confinement via membrane tension, allowing for compression-sensitive changes in migration. Cell nuclei contain many nuclear bodies that form when their components phase separate and condense within permissive local regions within the nucleus. However, how sub-nuclear organisation and phase separation changes with cell confinement and compression is largely unknown. Here we focus on paraspeckles, stress-responsive subnuclear bodies that form by phase separation around the long non-coding RNA NEAT1. As cells entered moderate confinement, a significant increase in paraspeckle number and size was observed compared to unconfined cells. Paraspeckle polarization bias towards the leading edge was also observed in confinement, correlating with regions of euchromatin. Increasing paraspeckle abundance resulted in increases in confined migration likelihood, speed, and directionality, as well as an enhancement of paraspeckle polarization towards the leading edge. This polarization of paraspeckle condensates may play a key role in regulating confined migration and invasion in cancer cells, and illustrates the utility of microchannel-based assays for identifying phenomena not observed on 2D or 3D bulk substrates. Nature Publishing Group UK 2023-02-03 /pmc/articles/PMC9898560/ /pubmed/36737664 http://dx.doi.org/10.1038/s42003-023-04528-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Todorovski, Vanja
McCluggage, Finn
Li, Yixuan
Meid, Annika
Spatz, Joachim P.
Holle, Andrew W.
Fox, Archa H.
Choi, Yu Suk
Confined environments induce polarized paraspeckle condensates
title Confined environments induce polarized paraspeckle condensates
title_full Confined environments induce polarized paraspeckle condensates
title_fullStr Confined environments induce polarized paraspeckle condensates
title_full_unstemmed Confined environments induce polarized paraspeckle condensates
title_short Confined environments induce polarized paraspeckle condensates
title_sort confined environments induce polarized paraspeckle condensates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9898560/
https://www.ncbi.nlm.nih.gov/pubmed/36737664
http://dx.doi.org/10.1038/s42003-023-04528-4
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