Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels

Conventional root canal treatment replaces the infected pulp with defined materials. Alternative cell-based tissue engineering strategies aim to regenerate a fully functional pulp within the root canal. Despite recent advances in this area, however, the regeneration of an innervated pulp remains a m...

Full description

Bibliographic Details
Main Authors: TT Madanagopal, YK Tai, SH Lim, CHH Fong, T Cao, V Rosa, A Franco-Obregón
Format: Article
Language:English
Published: AO Research Institute Davos 2021-03-01
Series:European Cells & Materials
Subjects:
Online Access:https://www.ecmjournal.org/papers/vol041/pdf/v041a16.pdf
id doaj-65ca54705be6469181b0da3bcb920a92
record_format Article
spelling doaj-65ca54705be6469181b0da3bcb920a922021-03-01T09:38:37Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622021-03-014121623210.22203/eCM.v041a16Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channelsTT MadanagopalYK TaiSH LimCHH FongT CaoV RosaA Franco-ObregónConventional root canal treatment replaces the infected pulp with defined materials. Alternative cell-based tissue engineering strategies aim to regenerate a fully functional pulp within the root canal. Despite recent advances in this area, however, the regeneration of an innervated pulp remains a major challenge in the field. Both graphene (2DG) and pulsed electromagnetic fields (PEMFs) independently have been shown to promote diverse cellular developmental programs. The present study showed that 2DG promoted the neurogenic induction of human dental pulp stem cells (hDPSCs) by upregulating and accelerating the expression of mature neuronal markers. Notably, 2DG induced the highest expression of transient receptor potential canonical cation channel type 1 (TRPC1) during early neurogenesis. As brief PEMF exposure promotes in vitro differentiation by activating a TRPC1-mitochondrial axis, an opportunity to combine 2DG with developmentally targeted PEMF exposure for synergistic effects was realizable. Neurogenic gene expression, neurotransmitter release, and reactive oxygen species (ROS) production were greatly enhanced by a brief (10 min) and low amplitude (2 mT) PEMF exposure timed to coincide with the highest TRPC1 expression from hDPSCs on 2DG. In contrast, hDPSCs on glass were less responsive to PEMF exposure. The capacity of PEMFs to promote neurogenesis was precluded by the administration of penicillin/streptomycin, mirroring previous studies demonstrating that aminoglycoside antibiotics block TRPC1-mediated calcium entry and verifying the contribution of TRPC1 in this form of magnetoreception. Hence, graphene created a more conducive environment for subsequent PEMF-stimulated neurogenic induction of hDPSCs through their mutual capacity to activate TRPC1with subsequent ROS production.https://www.ecmjournal.org/papers/vol041/pdf/v041a16.pdfpulsed electromagnetic fieldsmitohormesistissue engineeringnanomaterialpulp regeneration
collection DOAJ
language English
format Article
sources DOAJ
author TT Madanagopal
YK Tai
SH Lim
CHH Fong
T Cao
V Rosa
A Franco-Obregón
spellingShingle TT Madanagopal
YK Tai
SH Lim
CHH Fong
T Cao
V Rosa
A Franco-Obregón
Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
European Cells & Materials
pulsed electromagnetic fields
mitohormesis
tissue engineering
nanomaterial
pulp regeneration
author_facet TT Madanagopal
YK Tai
SH Lim
CHH Fong
T Cao
V Rosa
A Franco-Obregón
author_sort TT Madanagopal
title Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
title_short Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
title_full Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
title_fullStr Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
title_full_unstemmed Pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting TRPC1 channels
title_sort pulsed electromagnetic fields synergize with graphene to enhance dental pulp stem cell-derived neurogenesis by selectively targeting trpc1 channels
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2021-03-01
description Conventional root canal treatment replaces the infected pulp with defined materials. Alternative cell-based tissue engineering strategies aim to regenerate a fully functional pulp within the root canal. Despite recent advances in this area, however, the regeneration of an innervated pulp remains a major challenge in the field. Both graphene (2DG) and pulsed electromagnetic fields (PEMFs) independently have been shown to promote diverse cellular developmental programs. The present study showed that 2DG promoted the neurogenic induction of human dental pulp stem cells (hDPSCs) by upregulating and accelerating the expression of mature neuronal markers. Notably, 2DG induced the highest expression of transient receptor potential canonical cation channel type 1 (TRPC1) during early neurogenesis. As brief PEMF exposure promotes in vitro differentiation by activating a TRPC1-mitochondrial axis, an opportunity to combine 2DG with developmentally targeted PEMF exposure for synergistic effects was realizable. Neurogenic gene expression, neurotransmitter release, and reactive oxygen species (ROS) production were greatly enhanced by a brief (10 min) and low amplitude (2 mT) PEMF exposure timed to coincide with the highest TRPC1 expression from hDPSCs on 2DG. In contrast, hDPSCs on glass were less responsive to PEMF exposure. The capacity of PEMFs to promote neurogenesis was precluded by the administration of penicillin/streptomycin, mirroring previous studies demonstrating that aminoglycoside antibiotics block TRPC1-mediated calcium entry and verifying the contribution of TRPC1 in this form of magnetoreception. Hence, graphene created a more conducive environment for subsequent PEMF-stimulated neurogenic induction of hDPSCs through their mutual capacity to activate TRPC1with subsequent ROS production.
topic pulsed electromagnetic fields
mitohormesis
tissue engineering
nanomaterial
pulp regeneration
url https://www.ecmjournal.org/papers/vol041/pdf/v041a16.pdf
work_keys_str_mv AT ttmadanagopal pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT yktai pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT shlim pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT chhfong pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT tcao pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT vrosa pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
AT afrancoobregon pulsedelectromagneticfieldssynergizewithgraphenetoenhancedentalpulpstemcellderivedneurogenesisbyselectivelytargetingtrpc1channels
_version_ 1724246810746159104