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Humanized Biomimetic Nanovesicles for Neuron Targeting

Nanovesicles (NVs) are emerging as innovative, theranostic tools for cargo delivery. Recently, surface engineering of NVs with membrane proteins from specific cell types has been shown to improve the biocompatibility of NVs and enable the integration of functional attributes. However, this type of b...

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Autores principales: Zinger, Assaf, Cvetkovic, Caroline, Sushnitha, Manuela, Naoi, Tomoyuki, Baudo, Gherardo, Anderson, Morgan, Shetty, Arya, Basu, Nupur, Covello, Jennifer, Tasciotti, Ennio, Amit, Moran, Xie, Tongxin, Taraballi, Francesca, Krencik, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498895/
https://www.ncbi.nlm.nih.gov/pubmed/34382379
http://dx.doi.org/10.1002/advs.202101437
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author Zinger, Assaf
Cvetkovic, Caroline
Sushnitha, Manuela
Naoi, Tomoyuki
Baudo, Gherardo
Anderson, Morgan
Shetty, Arya
Basu, Nupur
Covello, Jennifer
Tasciotti, Ennio
Amit, Moran
Xie, Tongxin
Taraballi, Francesca
Krencik, Robert
author_facet Zinger, Assaf
Cvetkovic, Caroline
Sushnitha, Manuela
Naoi, Tomoyuki
Baudo, Gherardo
Anderson, Morgan
Shetty, Arya
Basu, Nupur
Covello, Jennifer
Tasciotti, Ennio
Amit, Moran
Xie, Tongxin
Taraballi, Francesca
Krencik, Robert
author_sort Zinger, Assaf
collection PubMed
description Nanovesicles (NVs) are emerging as innovative, theranostic tools for cargo delivery. Recently, surface engineering of NVs with membrane proteins from specific cell types has been shown to improve the biocompatibility of NVs and enable the integration of functional attributes. However, this type of biomimetic approach has not yet been explored using human neural cells for applications within the nervous system. Here, this paper optimizes and validates the scalable and reproducible production of two types of neuron‐targeting NVs, each with a distinct lipid formulation backbone suited to potential therapeutic cargo, by integrating membrane proteins that are unbiasedly sourced from human pluripotent stem‐cell‐derived neurons. The results establish that both endogenous and genetically engineered cell‐derived proteins effectively transfer to NVs without disruption of their physicochemical properties. NVs with neuron‐derived membrane proteins exhibit enhanced neuronal association and uptake compared to bare NVs. Viability of 3D neural sphere cultures is not disrupted by treatment, which verifies the utility of organoid‐based approaches as NV testing platforms. Finally, these results confirm cellular association and uptake of the biomimetic humanized NVs to neurons within rodent cranial nerves. In summary, the customizable NVs reported here enable next‐generation functionalized theranostics aimed to promote neuroregeneration.
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spelling pubmed-84988952021-10-12 Humanized Biomimetic Nanovesicles for Neuron Targeting Zinger, Assaf Cvetkovic, Caroline Sushnitha, Manuela Naoi, Tomoyuki Baudo, Gherardo Anderson, Morgan Shetty, Arya Basu, Nupur Covello, Jennifer Tasciotti, Ennio Amit, Moran Xie, Tongxin Taraballi, Francesca Krencik, Robert Adv Sci (Weinh) Research Article Nanovesicles (NVs) are emerging as innovative, theranostic tools for cargo delivery. Recently, surface engineering of NVs with membrane proteins from specific cell types has been shown to improve the biocompatibility of NVs and enable the integration of functional attributes. However, this type of biomimetic approach has not yet been explored using human neural cells for applications within the nervous system. Here, this paper optimizes and validates the scalable and reproducible production of two types of neuron‐targeting NVs, each with a distinct lipid formulation backbone suited to potential therapeutic cargo, by integrating membrane proteins that are unbiasedly sourced from human pluripotent stem‐cell‐derived neurons. The results establish that both endogenous and genetically engineered cell‐derived proteins effectively transfer to NVs without disruption of their physicochemical properties. NVs with neuron‐derived membrane proteins exhibit enhanced neuronal association and uptake compared to bare NVs. Viability of 3D neural sphere cultures is not disrupted by treatment, which verifies the utility of organoid‐based approaches as NV testing platforms. Finally, these results confirm cellular association and uptake of the biomimetic humanized NVs to neurons within rodent cranial nerves. In summary, the customizable NVs reported here enable next‐generation functionalized theranostics aimed to promote neuroregeneration. John Wiley and Sons Inc. 2021-08-11 /pmc/articles/PMC8498895/ /pubmed/34382379 http://dx.doi.org/10.1002/advs.202101437 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zinger, Assaf
Cvetkovic, Caroline
Sushnitha, Manuela
Naoi, Tomoyuki
Baudo, Gherardo
Anderson, Morgan
Shetty, Arya
Basu, Nupur
Covello, Jennifer
Tasciotti, Ennio
Amit, Moran
Xie, Tongxin
Taraballi, Francesca
Krencik, Robert
Humanized Biomimetic Nanovesicles for Neuron Targeting
title Humanized Biomimetic Nanovesicles for Neuron Targeting
title_full Humanized Biomimetic Nanovesicles for Neuron Targeting
title_fullStr Humanized Biomimetic Nanovesicles for Neuron Targeting
title_full_unstemmed Humanized Biomimetic Nanovesicles for Neuron Targeting
title_short Humanized Biomimetic Nanovesicles for Neuron Targeting
title_sort humanized biomimetic nanovesicles for neuron targeting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8498895/
https://www.ncbi.nlm.nih.gov/pubmed/34382379
http://dx.doi.org/10.1002/advs.202101437
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