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Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization
BACKGROUND: Accidental peripheral nerve injury during surgical intervention results in a broad spectrum of potentially debilitating side effects. Tissue distortion and poor visibility can significantly increase the risk of nerve injury with long-lasting consequences for the patient. We developed and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225226/ https://www.ncbi.nlm.nih.gov/pubmed/32409881 http://dx.doi.org/10.1186/s13550-020-00630-4 |
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author | Gonzales, Junior Pirovano, Giacomo Chow, Chun Yuen de Souza Franca, Paula Demetrio Carter, Lukas M. Klint, Julie K. Guru, Navjot Lewis, Jason S. King, Glenn F. Reiner, Thomas |
author_facet | Gonzales, Junior Pirovano, Giacomo Chow, Chun Yuen de Souza Franca, Paula Demetrio Carter, Lukas M. Klint, Julie K. Guru, Navjot Lewis, Jason S. King, Glenn F. Reiner, Thomas |
author_sort | Gonzales, Junior |
collection | PubMed |
description | BACKGROUND: Accidental peripheral nerve injury during surgical intervention results in a broad spectrum of potentially debilitating side effects. Tissue distortion and poor visibility can significantly increase the risk of nerve injury with long-lasting consequences for the patient. We developed and characterized Hs1a-FL, a fluorescent near-infrared molecule for nerve visualization in the operating theater with the aim of helping physicians to visualize nerves during surgery. Hs1a was derived from the venom of the Chinese bird spider, Haplopelma schmidti, and conjugated to Cy7.5 dye. Hs1a-FL was injected intravenously in mice, and harvested nerves were imaged microscopically and with epifluorescence. RESULTS: Hs1a-FL showed specific and stable binding to the sodium channel Na(V)1.7, present on the surface of human and mouse nerves. Hs1a-FL allowed epifluorescence visualization of sciatic mouse nerves with favorable nerve-to-muscle contrast. CONCLUSIONS: Fluorescent Na(V)1.7-targeted tracers have the potential to be adopted clinically for the intraoperative visualization of peripheral nerves during surgery, providing guidance for the surgeon and potentially improving the standard of care. |
format | Online Article Text |
id | pubmed-7225226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-72252262020-05-18 Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization Gonzales, Junior Pirovano, Giacomo Chow, Chun Yuen de Souza Franca, Paula Demetrio Carter, Lukas M. Klint, Julie K. Guru, Navjot Lewis, Jason S. King, Glenn F. Reiner, Thomas EJNMMI Res Original Research BACKGROUND: Accidental peripheral nerve injury during surgical intervention results in a broad spectrum of potentially debilitating side effects. Tissue distortion and poor visibility can significantly increase the risk of nerve injury with long-lasting consequences for the patient. We developed and characterized Hs1a-FL, a fluorescent near-infrared molecule for nerve visualization in the operating theater with the aim of helping physicians to visualize nerves during surgery. Hs1a was derived from the venom of the Chinese bird spider, Haplopelma schmidti, and conjugated to Cy7.5 dye. Hs1a-FL was injected intravenously in mice, and harvested nerves were imaged microscopically and with epifluorescence. RESULTS: Hs1a-FL showed specific and stable binding to the sodium channel Na(V)1.7, present on the surface of human and mouse nerves. Hs1a-FL allowed epifluorescence visualization of sciatic mouse nerves with favorable nerve-to-muscle contrast. CONCLUSIONS: Fluorescent Na(V)1.7-targeted tracers have the potential to be adopted clinically for the intraoperative visualization of peripheral nerves during surgery, providing guidance for the surgeon and potentially improving the standard of care. Springer Berlin Heidelberg 2020-05-14 /pmc/articles/PMC7225226/ /pubmed/32409881 http://dx.doi.org/10.1186/s13550-020-00630-4 Text en © The Author(s) 2020 Open AccessThis 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 | Original Research Gonzales, Junior Pirovano, Giacomo Chow, Chun Yuen de Souza Franca, Paula Demetrio Carter, Lukas M. Klint, Julie K. Guru, Navjot Lewis, Jason S. King, Glenn F. Reiner, Thomas Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title | Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title_full | Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title_fullStr | Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title_full_unstemmed | Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title_short | Fluorescence labeling of a Na(V)1.7-targeted peptide for near-infrared nerve visualization |
title_sort | fluorescence labeling of a na(v)1.7-targeted peptide for near-infrared nerve visualization |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225226/ https://www.ncbi.nlm.nih.gov/pubmed/32409881 http://dx.doi.org/10.1186/s13550-020-00630-4 |
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