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Spatial temperature gradients guide axonal outgrowth

Formation of neural networks during development and regeneration after injury depends on accuracy of axonal pathfinding, which is primarily believed to be influenced by chemical cues. Recently, there is growing evidence that physical cues can play crucial role in axonal guidance. However, detailed m...

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Autores principales: Black, Bryan, Vishwakarma, Vivek, Dhakal, Kamal, Bhattarai, Samik, Pradhan, Prabhakar, Jain, Ankur, Kim, Young-tae, Mohanty, Samarendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962095/
https://www.ncbi.nlm.nih.gov/pubmed/27460512
http://dx.doi.org/10.1038/srep29876
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author Black, Bryan
Vishwakarma, Vivek
Dhakal, Kamal
Bhattarai, Samik
Pradhan, Prabhakar
Jain, Ankur
Kim, Young-tae
Mohanty, Samarendra
author_facet Black, Bryan
Vishwakarma, Vivek
Dhakal, Kamal
Bhattarai, Samik
Pradhan, Prabhakar
Jain, Ankur
Kim, Young-tae
Mohanty, Samarendra
author_sort Black, Bryan
collection PubMed
description Formation of neural networks during development and regeneration after injury depends on accuracy of axonal pathfinding, which is primarily believed to be influenced by chemical cues. Recently, there is growing evidence that physical cues can play crucial role in axonal guidance. However, detailed mechanism involved in such guidance cues is lacking. By using weakly-focused near-infrared continuous wave (CW) laser microbeam in the path of an advancing axon, we discovered that the beam acts as a repulsive guidance cue. Here, we report that this highly-effective at-a-distance guidance is the result of a temperature field produced by the near-infrared laser light absorption. Since light absorption by extracellular medium increases when the laser wavelength was red shifted, the threshold laser power for reliable guidance was significantly lower in the near-infrared as compared to the visible spectrum. The spatial temperature gradient caused by the near-infrared laser beam at-a-distance was found to activate temperature-sensitive membrane receptors, resulting in an influx of calcium. The repulsive guidance effect was significantly reduced when extracellular calcium was depleted or in the presence of TRPV1-antagonist. Further, direct heating using micro-heater confirmed that the axonal guidance is caused by shallow temperature-gradient, eliminating the role of any non-photothermal effects.
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spelling pubmed-49620952016-08-08 Spatial temperature gradients guide axonal outgrowth Black, Bryan Vishwakarma, Vivek Dhakal, Kamal Bhattarai, Samik Pradhan, Prabhakar Jain, Ankur Kim, Young-tae Mohanty, Samarendra Sci Rep Article Formation of neural networks during development and regeneration after injury depends on accuracy of axonal pathfinding, which is primarily believed to be influenced by chemical cues. Recently, there is growing evidence that physical cues can play crucial role in axonal guidance. However, detailed mechanism involved in such guidance cues is lacking. By using weakly-focused near-infrared continuous wave (CW) laser microbeam in the path of an advancing axon, we discovered that the beam acts as a repulsive guidance cue. Here, we report that this highly-effective at-a-distance guidance is the result of a temperature field produced by the near-infrared laser light absorption. Since light absorption by extracellular medium increases when the laser wavelength was red shifted, the threshold laser power for reliable guidance was significantly lower in the near-infrared as compared to the visible spectrum. The spatial temperature gradient caused by the near-infrared laser beam at-a-distance was found to activate temperature-sensitive membrane receptors, resulting in an influx of calcium. The repulsive guidance effect was significantly reduced when extracellular calcium was depleted or in the presence of TRPV1-antagonist. Further, direct heating using micro-heater confirmed that the axonal guidance is caused by shallow temperature-gradient, eliminating the role of any non-photothermal effects. Nature Publishing Group 2016-07-27 /pmc/articles/PMC4962095/ /pubmed/27460512 http://dx.doi.org/10.1038/srep29876 Text en Copyright © 2016, 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
Black, Bryan
Vishwakarma, Vivek
Dhakal, Kamal
Bhattarai, Samik
Pradhan, Prabhakar
Jain, Ankur
Kim, Young-tae
Mohanty, Samarendra
Spatial temperature gradients guide axonal outgrowth
title Spatial temperature gradients guide axonal outgrowth
title_full Spatial temperature gradients guide axonal outgrowth
title_fullStr Spatial temperature gradients guide axonal outgrowth
title_full_unstemmed Spatial temperature gradients guide axonal outgrowth
title_short Spatial temperature gradients guide axonal outgrowth
title_sort spatial temperature gradients guide axonal outgrowth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962095/
https://www.ncbi.nlm.nih.gov/pubmed/27460512
http://dx.doi.org/10.1038/srep29876
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