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Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals
Selective in vivo delivery of cargo to peripheral nervous system (PNS) has broad clinical and preclinical applications. An important applicability of this approach is systemic delivery of fluorescently conjugated ligands that selectively label PNS, which could allow visualization of peripheral nerve...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626805/ https://www.ncbi.nlm.nih.gov/pubmed/26514366 http://dx.doi.org/10.1038/srep15766 |
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author | Massaad, Cynthia A. Zhang, Gang Pillai, Laila Azhdarinia, Ali Liu, Weiqiang Sheikh, Kazim A. |
author_facet | Massaad, Cynthia A. Zhang, Gang Pillai, Laila Azhdarinia, Ali Liu, Weiqiang Sheikh, Kazim A. |
author_sort | Massaad, Cynthia A. |
collection | PubMed |
description | Selective in vivo delivery of cargo to peripheral nervous system (PNS) has broad clinical and preclinical applications. An important applicability of this approach is systemic delivery of fluorescently conjugated ligands that selectively label PNS, which could allow visualization of peripheral nerves during any surgery. We examine the use of an anti-ganglioside monoclonal antibody (mAb) as selective neuronal delivery vector for surgical imaging of peripheral nerves. Systemic delivery of an anti-ganglioside mAb was used for selective intraneuronal/axonal delivery of fluorescent agents to visualize nerves by surgical imaging in living mice. In this study, we show that intact motor, sensory, and autonomic nerve fibers/paths are distinctly labeled following a single nanomolar systemic injection of fluorescently labeled anti-ganglioside mAb. Tissue biodistribution studies with radiolabeled mAb were used to validate neuronal uptake of fluorescently labeled mAb. Implications of this proof of concept study are that fluorescent conjugates of anti-ganglioside mAbs are valuable delivery vectors to visualize nerves during surgery to avoid nerve injury and monitor nerve degeneration and regeneration after injury. These findings support that antibodies, and their derivatives/fragments, can be used as selective neuronal delivery vector for transport of various cargos to PNS in preclinical and clinical settings. |
format | Online Article Text |
id | pubmed-4626805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46268052015-11-03 Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals Massaad, Cynthia A. Zhang, Gang Pillai, Laila Azhdarinia, Ali Liu, Weiqiang Sheikh, Kazim A. Sci Rep Article Selective in vivo delivery of cargo to peripheral nervous system (PNS) has broad clinical and preclinical applications. An important applicability of this approach is systemic delivery of fluorescently conjugated ligands that selectively label PNS, which could allow visualization of peripheral nerves during any surgery. We examine the use of an anti-ganglioside monoclonal antibody (mAb) as selective neuronal delivery vector for surgical imaging of peripheral nerves. Systemic delivery of an anti-ganglioside mAb was used for selective intraneuronal/axonal delivery of fluorescent agents to visualize nerves by surgical imaging in living mice. In this study, we show that intact motor, sensory, and autonomic nerve fibers/paths are distinctly labeled following a single nanomolar systemic injection of fluorescently labeled anti-ganglioside mAb. Tissue biodistribution studies with radiolabeled mAb were used to validate neuronal uptake of fluorescently labeled mAb. Implications of this proof of concept study are that fluorescent conjugates of anti-ganglioside mAbs are valuable delivery vectors to visualize nerves during surgery to avoid nerve injury and monitor nerve degeneration and regeneration after injury. These findings support that antibodies, and their derivatives/fragments, can be used as selective neuronal delivery vector for transport of various cargos to PNS in preclinical and clinical settings. Nature Publishing Group 2015-10-30 /pmc/articles/PMC4626805/ /pubmed/26514366 http://dx.doi.org/10.1038/srep15766 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Massaad, Cynthia A. Zhang, Gang Pillai, Laila Azhdarinia, Ali Liu, Weiqiang Sheikh, Kazim A. Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title | Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title_full | Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title_fullStr | Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title_full_unstemmed | Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title_short | Fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
title_sort | fluorescently-tagged anti-ganglioside antibody selectively identifies peripheral nerve in living animals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626805/ https://www.ncbi.nlm.nih.gov/pubmed/26514366 http://dx.doi.org/10.1038/srep15766 |
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