Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine

Peripheral nerve regeneration is a slow process that can be associated with limited outcomes and thus, a search for novel and effective therapy for peripheral nerve injury and disease is crucial. Here, we found that roscovitine, a synthetic purine nucleoside analog, enhances neurite outgrowth in ne...

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Main Authors: Vincent Law, Sophi Dong, Jesusa L. Rosales, Myung-Yung Jeong, Douglas Zochodne, Ki-Young Lee
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-10-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2016.00238/full
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spelling doaj-ebfe9b8339704000ab1aa31b163625b02020-11-24T21:06:59ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022016-10-011010.3389/fncel.2016.00238219878Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitineVincent Law0Sophi Dong1Jesusa L. Rosales2Myung-Yung Jeong3Douglas Zochodne4Ki-Young Lee5University of CalgaryUniversity of CalgaryUniversity of CalgaryPusan National UniversityUniversity of CalgaryUniversity of CalgaryPeripheral nerve regeneration is a slow process that can be associated with limited outcomes and thus, a search for novel and effective therapy for peripheral nerve injury and disease is crucial. Here, we found that roscovitine, a synthetic purine nucleoside analog, enhances neurite outgrowth in neuronal-like PC12 cells. Furthermore, ex vivo analysis of pre-injured adult rat dorsal root ganglion neurons showed that roscovitine enhances neurite regrowth in these cells. Likewise, in vivo transected sciatic nerves in rats locally perfused with roscovitine had augmented repopulation of new myelinated axons beyond the transection zone. By mass spectrometry, we found that roscovitine interacts with tubulin and actin. It interacts directly with tubulin and causes a dose-dependent induction of tubulin polymerization as well as enhances GTP-dependent tubulin polymerization. Conversely, roscovitine interacts indirectly with actin and counteracts the inhibitory effect of Cdk5 on Arp2/3-dependent actin polymerization, and thus, causes actin polymerization. Moreover, in the presence of neurotrophic factors such as NGF, roscovitine-enhanced neurite outgrowth is mediated by increased activation of the ERK1/2 and p38 MAPK pathways. Since microtubule and F-actin dynamics are critical for axonal regrowth, the ability of roscovitine to activate the ERK1/2 and p38 MAPK pathways, and support polymerization of tubulin and actin indicate a major role for this purine nucleoside analog in the promotion of axonal regeneration. Together, our findings demonstrate a therapeutic potential for the purine nucleoside analog, roscovitine, in peripheral nerve injury.http://journal.frontiersin.org/Journal/10.3389/fncel.2016.00238/fullCytoskeletonRegenerationperipheral nerveAxoninjury
collection DOAJ
language English
format Article
sources DOAJ
author Vincent Law
Sophi Dong
Jesusa L. Rosales
Myung-Yung Jeong
Douglas Zochodne
Ki-Young Lee
spellingShingle Vincent Law
Sophi Dong
Jesusa L. Rosales
Myung-Yung Jeong
Douglas Zochodne
Ki-Young Lee
Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
Frontiers in Cellular Neuroscience
Cytoskeleton
Regeneration
peripheral nerve
Axon
injury
author_facet Vincent Law
Sophi Dong
Jesusa L. Rosales
Myung-Yung Jeong
Douglas Zochodne
Ki-Young Lee
author_sort Vincent Law
title Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
title_short Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
title_full Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
title_fullStr Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
title_full_unstemmed Enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
title_sort enhancement of peripheral nerve regrowth by the purine nucleoside analog and cell cycle inhibitor, roscovitine
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2016-10-01
description Peripheral nerve regeneration is a slow process that can be associated with limited outcomes and thus, a search for novel and effective therapy for peripheral nerve injury and disease is crucial. Here, we found that roscovitine, a synthetic purine nucleoside analog, enhances neurite outgrowth in neuronal-like PC12 cells. Furthermore, ex vivo analysis of pre-injured adult rat dorsal root ganglion neurons showed that roscovitine enhances neurite regrowth in these cells. Likewise, in vivo transected sciatic nerves in rats locally perfused with roscovitine had augmented repopulation of new myelinated axons beyond the transection zone. By mass spectrometry, we found that roscovitine interacts with tubulin and actin. It interacts directly with tubulin and causes a dose-dependent induction of tubulin polymerization as well as enhances GTP-dependent tubulin polymerization. Conversely, roscovitine interacts indirectly with actin and counteracts the inhibitory effect of Cdk5 on Arp2/3-dependent actin polymerization, and thus, causes actin polymerization. Moreover, in the presence of neurotrophic factors such as NGF, roscovitine-enhanced neurite outgrowth is mediated by increased activation of the ERK1/2 and p38 MAPK pathways. Since microtubule and F-actin dynamics are critical for axonal regrowth, the ability of roscovitine to activate the ERK1/2 and p38 MAPK pathways, and support polymerization of tubulin and actin indicate a major role for this purine nucleoside analog in the promotion of axonal regeneration. Together, our findings demonstrate a therapeutic potential for the purine nucleoside analog, roscovitine, in peripheral nerve injury.
topic Cytoskeleton
Regeneration
peripheral nerve
Axon
injury
url http://journal.frontiersin.org/Journal/10.3389/fncel.2016.00238/full
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