Cargando…

Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells

The axon regeneration of neurons in the brain can be enhanced by activating intracellular signaling pathways such as those triggered by the membrane-anchored Rat sarcoma (RAS) proto-oncogene. Here we demonstrate the induction of neurite growth by expressing tagged permanently active Harvey-RAS prote...

Descripción completa

Detalles Bibliográficos
Autores principales: Raudzus, Fabian, Schöneborn, Hendrik, Neumann, Sebastian, Secret, Emilie, Michel, Aude, Fresnais, Jérome, Brylski, Oliver, Ménager, Christine, Siaugue, Jean-Michel, Heumann, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775457/
https://www.ncbi.nlm.nih.gov/pubmed/33384447
http://dx.doi.org/10.1038/s41598-020-80253-w
_version_ 1783630470599147520
author Raudzus, Fabian
Schöneborn, Hendrik
Neumann, Sebastian
Secret, Emilie
Michel, Aude
Fresnais, Jérome
Brylski, Oliver
Ménager, Christine
Siaugue, Jean-Michel
Heumann, Rolf
author_facet Raudzus, Fabian
Schöneborn, Hendrik
Neumann, Sebastian
Secret, Emilie
Michel, Aude
Fresnais, Jérome
Brylski, Oliver
Ménager, Christine
Siaugue, Jean-Michel
Heumann, Rolf
author_sort Raudzus, Fabian
collection PubMed
description The axon regeneration of neurons in the brain can be enhanced by activating intracellular signaling pathways such as those triggered by the membrane-anchored Rat sarcoma (RAS) proto-oncogene. Here we demonstrate the induction of neurite growth by expressing tagged permanently active Harvey-RAS protein or the RAS-activating catalytic domain of the guanine nucleotide exchange factor (SOS1cat), in secondary dopaminergic cells. Due to the tag, the expressed fusion protein is captured by functionalized magnetic nanoparticles in the cytoplasm of the cell. We use magnetic tips for remote translocation of the SOS1cat-loaded magnetic nanoparticles from the cytoplasm towards the inner face of the plasma membrane where the endogenous Harvey-RAS protein is located. Furthermore, we show the magnetic transport of SOS1cat-bound nanoparticles from the cytoplasm into the neurite until they accumulate at its tip on a time scale of minutes. In order to scale-up from single cells, we show the cytoplasmic delivery of the magnetic nanoparticles into large numbers of cells without changing the cellular response to nerve growth factor. These results will serve as an initial step to develop tools for refining cell replacement therapies based on grafted human induced dopaminergic neurons loaded with functionalized magnetic nanoparticles in Parkinson model systems.
format Online
Article
Text
id pubmed-7775457
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-77754572021-01-07 Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells Raudzus, Fabian Schöneborn, Hendrik Neumann, Sebastian Secret, Emilie Michel, Aude Fresnais, Jérome Brylski, Oliver Ménager, Christine Siaugue, Jean-Michel Heumann, Rolf Sci Rep Article The axon regeneration of neurons in the brain can be enhanced by activating intracellular signaling pathways such as those triggered by the membrane-anchored Rat sarcoma (RAS) proto-oncogene. Here we demonstrate the induction of neurite growth by expressing tagged permanently active Harvey-RAS protein or the RAS-activating catalytic domain of the guanine nucleotide exchange factor (SOS1cat), in secondary dopaminergic cells. Due to the tag, the expressed fusion protein is captured by functionalized magnetic nanoparticles in the cytoplasm of the cell. We use magnetic tips for remote translocation of the SOS1cat-loaded magnetic nanoparticles from the cytoplasm towards the inner face of the plasma membrane where the endogenous Harvey-RAS protein is located. Furthermore, we show the magnetic transport of SOS1cat-bound nanoparticles from the cytoplasm into the neurite until they accumulate at its tip on a time scale of minutes. In order to scale-up from single cells, we show the cytoplasmic delivery of the magnetic nanoparticles into large numbers of cells without changing the cellular response to nerve growth factor. These results will serve as an initial step to develop tools for refining cell replacement therapies based on grafted human induced dopaminergic neurons loaded with functionalized magnetic nanoparticles in Parkinson model systems. Nature Publishing Group UK 2020-12-31 /pmc/articles/PMC7775457/ /pubmed/33384447 http://dx.doi.org/10.1038/s41598-020-80253-w Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Raudzus, Fabian
Schöneborn, Hendrik
Neumann, Sebastian
Secret, Emilie
Michel, Aude
Fresnais, Jérome
Brylski, Oliver
Ménager, Christine
Siaugue, Jean-Michel
Heumann, Rolf
Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title_full Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title_fullStr Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title_full_unstemmed Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title_short Magnetic spatiotemporal control of SOS1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
title_sort magnetic spatiotemporal control of sos1 coupled nanoparticles for guided neurite growth in dopaminergic single cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775457/
https://www.ncbi.nlm.nih.gov/pubmed/33384447
http://dx.doi.org/10.1038/s41598-020-80253-w
work_keys_str_mv AT raudzusfabian magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT schonebornhendrik magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT neumannsebastian magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT secretemilie magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT michelaude magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT fresnaisjerome magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT brylskioliver magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT menagerchristine magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT siauguejeanmichel magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells
AT heumannrolf magneticspatiotemporalcontrolofsos1couplednanoparticlesforguidedneuritegrowthindopaminergicsinglecells