Cargando…
The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes
Inflammatory cells acquire a polarized phenotype to migrate towards sites of infection or injury. A conserved polarity complex comprising PAR-3, PAR-6 and atypical protein kinase C (aPKC) relays extracellular polarizing cues to control cytoskeletal and signaling networks affecting morphological and...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197085/ https://www.ncbi.nlm.nih.gov/pubmed/25179599 http://dx.doi.org/10.1242/jcs.146217 |
_version_ | 1782339565413990400 |
---|---|
author | Crespo, Carolina Lage Vernieri, Claudio Keller, Philipp J. Garrè, Massimiliano Bender, Jeffrey R. Wittbrodt, Joachim Pardi, Ruggero |
author_facet | Crespo, Carolina Lage Vernieri, Claudio Keller, Philipp J. Garrè, Massimiliano Bender, Jeffrey R. Wittbrodt, Joachim Pardi, Ruggero |
author_sort | Crespo, Carolina Lage |
collection | PubMed |
description | Inflammatory cells acquire a polarized phenotype to migrate towards sites of infection or injury. A conserved polarity complex comprising PAR-3, PAR-6 and atypical protein kinase C (aPKC) relays extracellular polarizing cues to control cytoskeletal and signaling networks affecting morphological and functional polarization. However, there is no evidence that myeloid cells use PAR signaling to migrate vectorially in three-dimensional (3D) environments in vivo. Using genetically encoded bioprobes and high-resolution live imaging, we reveal the existence of F-actin oscillations in the trailing edge and constant repositioning of the microtubule organizing center (MTOC) to direct leukocyte migration in wounded medaka fish larvae (Oryzias latipes). Genetic manipulation in live myeloid cells demonstrates that the catalytic activity of aPKC and the regulated interaction with PAR-3 and PAR-6 are required for consistent F-actin oscillations, MTOC perinuclear mobility, aPKC repositioning and wound-directed migration upstream of Rho kinase (also known as ROCK or ROK) activation. We propose that the PAR complex coordinately controls cytoskeletal changes affecting both the generation of traction force and the directionality of leukocyte migration to sites of injury. |
format | Online Article Text |
id | pubmed-4197085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-41970852014-11-18 The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes Crespo, Carolina Lage Vernieri, Claudio Keller, Philipp J. Garrè, Massimiliano Bender, Jeffrey R. Wittbrodt, Joachim Pardi, Ruggero J Cell Sci Research Article Inflammatory cells acquire a polarized phenotype to migrate towards sites of infection or injury. A conserved polarity complex comprising PAR-3, PAR-6 and atypical protein kinase C (aPKC) relays extracellular polarizing cues to control cytoskeletal and signaling networks affecting morphological and functional polarization. However, there is no evidence that myeloid cells use PAR signaling to migrate vectorially in three-dimensional (3D) environments in vivo. Using genetically encoded bioprobes and high-resolution live imaging, we reveal the existence of F-actin oscillations in the trailing edge and constant repositioning of the microtubule organizing center (MTOC) to direct leukocyte migration in wounded medaka fish larvae (Oryzias latipes). Genetic manipulation in live myeloid cells demonstrates that the catalytic activity of aPKC and the regulated interaction with PAR-3 and PAR-6 are required for consistent F-actin oscillations, MTOC perinuclear mobility, aPKC repositioning and wound-directed migration upstream of Rho kinase (also known as ROCK or ROK) activation. We propose that the PAR complex coordinately controls cytoskeletal changes affecting both the generation of traction force and the directionality of leukocyte migration to sites of injury. The Company of Biologists 2014-10-15 /pmc/articles/PMC4197085/ /pubmed/25179599 http://dx.doi.org/10.1242/jcs.146217 Text en © 2014. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Crespo, Carolina Lage Vernieri, Claudio Keller, Philipp J. Garrè, Massimiliano Bender, Jeffrey R. Wittbrodt, Joachim Pardi, Ruggero The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title | The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title_full | The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title_fullStr | The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title_full_unstemmed | The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title_short | The PAR complex controls the spatiotemporal dynamics of F-actin and the MTOC in directionally migrating leukocytes |
title_sort | par complex controls the spatiotemporal dynamics of f-actin and the mtoc in directionally migrating leukocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197085/ https://www.ncbi.nlm.nih.gov/pubmed/25179599 http://dx.doi.org/10.1242/jcs.146217 |
work_keys_str_mv | AT crespocarolinalage theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT verniericlaudio theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT kellerphilippj theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT garremassimiliano theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT benderjeffreyr theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT wittbrodtjoachim theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT pardiruggero theparcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT crespocarolinalage parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT verniericlaudio parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT kellerphilippj parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT garremassimiliano parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT benderjeffreyr parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT wittbrodtjoachim parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes AT pardiruggero parcomplexcontrolsthespatiotemporaldynamicsoffactinandthemtocindirectionallymigratingleukocytes |