Cargando…

Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues

Neural interfaces are designed to decode motor intent and evoke sensory precepts in amputees. In peripheral nerves, recording movement intent is challenging because motor axons are only a small fraction compared to sensory fibers and are heterogeneously mixed particularly at proximal levels. We prev...

Descripción completa

Detalles Bibliográficos
Autores principales: Anand, Sanjay, Desai, Vidhi, Alsmadi, Nesreen, Kanneganti, Aswini, Nguyen, Dianna Huyen-Tram, Tran, Martin, Patil, Lokesh, Vasudevan, Srikanth, Xu, Cancan, Hong, Yi, Cheng, Jonathan, Keefer, Edward, Romero-Ortega, Mario I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662603/
https://www.ncbi.nlm.nih.gov/pubmed/29085079
http://dx.doi.org/10.1038/s41598-017-14331-x
_version_ 1783274662853083136
author Anand, Sanjay
Desai, Vidhi
Alsmadi, Nesreen
Kanneganti, Aswini
Nguyen, Dianna Huyen-Tram
Tran, Martin
Patil, Lokesh
Vasudevan, Srikanth
Xu, Cancan
Hong, Yi
Cheng, Jonathan
Keefer, Edward
Romero-Ortega, Mario I.
author_facet Anand, Sanjay
Desai, Vidhi
Alsmadi, Nesreen
Kanneganti, Aswini
Nguyen, Dianna Huyen-Tram
Tran, Martin
Patil, Lokesh
Vasudevan, Srikanth
Xu, Cancan
Hong, Yi
Cheng, Jonathan
Keefer, Edward
Romero-Ortega, Mario I.
author_sort Anand, Sanjay
collection PubMed
description Neural interfaces are designed to decode motor intent and evoke sensory precepts in amputees. In peripheral nerves, recording movement intent is challenging because motor axons are only a small fraction compared to sensory fibers and are heterogeneously mixed particularly at proximal levels. We previously reported that pain and myelinated axons regenerating through a Y-shaped nerve guide with sealed ends, can be modulated by luminar release of nerve growth factor (NGF) and neurotrophin-3 (NT-3), respectively. Here, we evaluate the differential potency of NGF, glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), pleiotrophin (PTN), and NT-3 in asymmetrically guiding the regeneration of sensory and motor neurons. We report that, in the absence of distal target organs, molecular guidance cues can mediate the growth of electrically conductive fascicles with normal microanatomy. Compared to Y-tube compartments with bovine serum albumin (BSA), GDNF and NGF increased the motor and sensory axon content, respectively. In addition, the sensory to motor ratio was significantly increased by PTN (12.7:1) when compared to a BDNF + GDNF choice. The differential content of motor and sensory axons modulated by selective guidance cues may provide a strategy to better define axon types in peripheral nerve interfaces.
format Online
Article
Text
id pubmed-5662603
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56626032017-11-08 Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues Anand, Sanjay Desai, Vidhi Alsmadi, Nesreen Kanneganti, Aswini Nguyen, Dianna Huyen-Tram Tran, Martin Patil, Lokesh Vasudevan, Srikanth Xu, Cancan Hong, Yi Cheng, Jonathan Keefer, Edward Romero-Ortega, Mario I. Sci Rep Article Neural interfaces are designed to decode motor intent and evoke sensory precepts in amputees. In peripheral nerves, recording movement intent is challenging because motor axons are only a small fraction compared to sensory fibers and are heterogeneously mixed particularly at proximal levels. We previously reported that pain and myelinated axons regenerating through a Y-shaped nerve guide with sealed ends, can be modulated by luminar release of nerve growth factor (NGF) and neurotrophin-3 (NT-3), respectively. Here, we evaluate the differential potency of NGF, glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), pleiotrophin (PTN), and NT-3 in asymmetrically guiding the regeneration of sensory and motor neurons. We report that, in the absence of distal target organs, molecular guidance cues can mediate the growth of electrically conductive fascicles with normal microanatomy. Compared to Y-tube compartments with bovine serum albumin (BSA), GDNF and NGF increased the motor and sensory axon content, respectively. In addition, the sensory to motor ratio was significantly increased by PTN (12.7:1) when compared to a BDNF + GDNF choice. The differential content of motor and sensory axons modulated by selective guidance cues may provide a strategy to better define axon types in peripheral nerve interfaces. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662603/ /pubmed/29085079 http://dx.doi.org/10.1038/s41598-017-14331-x Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Anand, Sanjay
Desai, Vidhi
Alsmadi, Nesreen
Kanneganti, Aswini
Nguyen, Dianna Huyen-Tram
Tran, Martin
Patil, Lokesh
Vasudevan, Srikanth
Xu, Cancan
Hong, Yi
Cheng, Jonathan
Keefer, Edward
Romero-Ortega, Mario I.
Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title_full Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title_fullStr Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title_full_unstemmed Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title_short Asymmetric Sensory-Motor Regeneration of Transected Peripheral Nerves Using Molecular Guidance Cues
title_sort asymmetric sensory-motor regeneration of transected peripheral nerves using molecular guidance cues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662603/
https://www.ncbi.nlm.nih.gov/pubmed/29085079
http://dx.doi.org/10.1038/s41598-017-14331-x
work_keys_str_mv AT anandsanjay asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT desaividhi asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT alsmadinesreen asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT kannegantiaswini asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT nguyendiannahuyentram asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT tranmartin asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT patillokesh asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT vasudevansrikanth asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT xucancan asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT hongyi asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT chengjonathan asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT keeferedward asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues
AT romeroortegamarioi asymmetricsensorymotorregenerationoftransectedperipheralnervesusingmolecularguidancecues