Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System

A critical role of the peripheral axons of nociceptors of the dorsal root ganglion (DRG) is the conduction of all-or-nothing action potentials from peripheral nerve endings to the central nervous system for the perception of noxious stimuli. Plasticity along multiple sites along the pain axis has no...

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Autores principales: Rahul Atmaramani, Srivennela Veeramachaneni, Liz Valeria Mogas, Pratik Koppikar, Bryan J. Black, Audrey Hammack, Joseph J. Pancrazio, Rafael Granja-Vazquez
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/a0cb8df00bdf4655b84585a36d724080
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spelling oai:doaj.org-article:a0cb8df00bdf4655b84585a36d7240802021-11-25T18:23:05ZInvestigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System10.3390/mi121113172072-666Xhttps://doaj.org/article/a0cb8df00bdf4655b84585a36d7240802021-10-01T00:00:00Zhttps://www.mdpi.com/2072-666X/12/11/1317https://doaj.org/toc/2072-666XA critical role of the peripheral axons of nociceptors of the dorsal root ganglion (DRG) is the conduction of all-or-nothing action potentials from peripheral nerve endings to the central nervous system for the perception of noxious stimuli. Plasticity along multiple sites along the pain axis has now been widely implicated in the maladaptive changes that occur in pathological pain states such as neuropathic and inflammatory pain. Notably, increasing evidence suggests that nociceptive axons actively participate through the local expression of ion channels, receptors, and signal transduction molecules through axonal mRNA translation machinery that is independent of the soma component. In this report, we explore the sensitization of sensory neurons through the treatment of compartmentalized axon-like structures spanning microchannels that have been treated with the cytokine IL-6 and, subsequently, capsaicin. These data demonstrate the utility of isolating DRG axon-like structures using microfluidic systems, laying the groundwork for constructing the complex in vitro models of cellular networks that are involved in pain signaling for targeted pharmacological and genetic perturbations.Rahul AtmaramaniSrivennela VeeramachaneniLiz Valeria MogasPratik KoppikarBryan J. BlackAudrey HammackJoseph J. PancrazioRafael Granja-VazquezMDPI AGarticlenociceptiondorsal root gangliaaxonal stimulationmaladaptive plasticitydrug discoverymicrofluidicsMechanical engineering and machineryTJ1-1570ENMicromachines, Vol 12, Iss 1317, p 1317 (2021)
institution DOAJ
collection DOAJ
language EN
topic nociception
dorsal root ganglia
axonal stimulation
maladaptive plasticity
drug discovery
microfluidics
Mechanical engineering and machinery
TJ1-1570
spellingShingle nociception
dorsal root ganglia
axonal stimulation
maladaptive plasticity
drug discovery
microfluidics
Mechanical engineering and machinery
TJ1-1570
Rahul Atmaramani
Srivennela Veeramachaneni
Liz Valeria Mogas
Pratik Koppikar
Bryan J. Black
Audrey Hammack
Joseph J. Pancrazio
Rafael Granja-Vazquez
Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
description A critical role of the peripheral axons of nociceptors of the dorsal root ganglion (DRG) is the conduction of all-or-nothing action potentials from peripheral nerve endings to the central nervous system for the perception of noxious stimuli. Plasticity along multiple sites along the pain axis has now been widely implicated in the maladaptive changes that occur in pathological pain states such as neuropathic and inflammatory pain. Notably, increasing evidence suggests that nociceptive axons actively participate through the local expression of ion channels, receptors, and signal transduction molecules through axonal mRNA translation machinery that is independent of the soma component. In this report, we explore the sensitization of sensory neurons through the treatment of compartmentalized axon-like structures spanning microchannels that have been treated with the cytokine IL-6 and, subsequently, capsaicin. These data demonstrate the utility of isolating DRG axon-like structures using microfluidic systems, laying the groundwork for constructing the complex in vitro models of cellular networks that are involved in pain signaling for targeted pharmacological and genetic perturbations.
format article
author Rahul Atmaramani
Srivennela Veeramachaneni
Liz Valeria Mogas
Pratik Koppikar
Bryan J. Black
Audrey Hammack
Joseph J. Pancrazio
Rafael Granja-Vazquez
author_facet Rahul Atmaramani
Srivennela Veeramachaneni
Liz Valeria Mogas
Pratik Koppikar
Bryan J. Black
Audrey Hammack
Joseph J. Pancrazio
Rafael Granja-Vazquez
author_sort Rahul Atmaramani
title Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
title_short Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
title_full Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
title_fullStr Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
title_full_unstemmed Investigating the Function of Adult DRG Neuron Axons Using an In Vitro Microfluidic Culture System
title_sort investigating the function of adult drg neuron axons using an in vitro microfluidic culture system
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/a0cb8df00bdf4655b84585a36d724080
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