Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix

Transplantation of olfactory ensheathing cells (OECs) is a promising approach for repairing the injured nervous system that has been extensively trialed for nervous system repair. However, the method still needs improvement and optimization. One avenue of improving outcomes is to stimulate OEC migra...

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Main Authors: Yu-Ting Tseng, Mo Chen, Richard Lai, Francesca Oieni, Graham Smyth, Shailendra Anoopkumar-Dukie, James St John, Jenny Ekberg
Format: Article
Language:English
Published: Elsevier 2021-09-01
Series:Biomedicine & Pharmacotherapy
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0753332221006016
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spelling doaj-44baec675f4a4381bb7d596e72370b282021-09-05T04:38:47ZengElsevierBiomedicine & Pharmacotherapy0753-33222021-09-01141111819Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrixYu-Ting Tseng0Mo Chen1Richard Lai2Francesca Oieni3Graham Smyth4Shailendra Anoopkumar-Dukie5James St John6Jenny Ekberg7Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, AustraliaMenzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, AustraliaMenzies Health Institute Queensland, Griffith University, Southport, QLD 4222, AustraliaMenzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, AustraliaMenzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, AustraliaSchool of Pharmacy and Medical Sciences, Griffith University, Southport, QLD 4222, AustraliaMenzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, Australia; Griffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia; Corresponding authors at: Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia.Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia; Clem Jones Centre for Neurobiology and Stem Cell Research, Griffith University, Brisbane, QLD 4111, Australia; School of Pharmacy and Medical Sciences, Griffith University, Southport, QLD 4222, Australia; Griffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia; Corresponding authors at: Menzies Health Institute Queensland, Griffith University, Southport, QLD 4222, Australia.Transplantation of olfactory ensheathing cells (OECs) is a promising approach for repairing the injured nervous system that has been extensively trialed for nervous system repair. However, the method still needs improvement and optimization. One avenue of improving outcomes is to stimulate OEC migration into the injury site. Liraglutide is a glucagon-like peptide-1 receptor agonist used for management of diabetes and obesity. It has been shown to be neuroprotective and to promote cell migration, but whether it can stimulate glial cells remains unknown. In the current study, we investigated the effects of liraglutide on OEC migration and explored the involved mechanisms. We showed that liraglutide at low concentration (100 nM) overall promoted OEC migration over time. Liraglutide modulated the migratory behavior of OECs by reducing time in arrest, and promoted random rather than straight migration. Liraglutide also induced a morphological change of primary OECs towards a bipolar shape consistent with improved migration. We found that liraglutide activated extracellular signal-regulated kinase (ERK), which has key roles in cell migration; the timing of ERK activation correlated with stimulation of migration. Furthermore, liraglutide also modulated the extracellular matrix by upregulating laminin-1 and down-regulating collagen IV. In summary, we found that liraglutide can stimulate OEC migration and re-model the extracellular matrix to better promote cell migration, and possibly also to become more conducive for axonal regeneration. Thus, liraglutide may improve OEC transplantation outcomes.http://www.sciencedirect.com/science/article/pii/S0753332221006016GliaExtracellular signal-regulated kinaseLaminin-1Collagen IVGLP-1RCell transplantation
collection DOAJ
language English
format Article
sources DOAJ
author Yu-Ting Tseng
Mo Chen
Richard Lai
Francesca Oieni
Graham Smyth
Shailendra Anoopkumar-Dukie
James St John
Jenny Ekberg
spellingShingle Yu-Ting Tseng
Mo Chen
Richard Lai
Francesca Oieni
Graham Smyth
Shailendra Anoopkumar-Dukie
James St John
Jenny Ekberg
Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
Biomedicine & Pharmacotherapy
Glia
Extracellular signal-regulated kinase
Laminin-1
Collagen IV
GLP-1R
Cell transplantation
author_facet Yu-Ting Tseng
Mo Chen
Richard Lai
Francesca Oieni
Graham Smyth
Shailendra Anoopkumar-Dukie
James St John
Jenny Ekberg
author_sort Yu-Ting Tseng
title Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
title_short Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
title_full Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
title_fullStr Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
title_full_unstemmed Liraglutide modulates olfactory ensheathing cell migration with activation of ERK and alteration of the extracellular matrix
title_sort liraglutide modulates olfactory ensheathing cell migration with activation of erk and alteration of the extracellular matrix
publisher Elsevier
series Biomedicine & Pharmacotherapy
issn 0753-3322
publishDate 2021-09-01
description Transplantation of olfactory ensheathing cells (OECs) is a promising approach for repairing the injured nervous system that has been extensively trialed for nervous system repair. However, the method still needs improvement and optimization. One avenue of improving outcomes is to stimulate OEC migration into the injury site. Liraglutide is a glucagon-like peptide-1 receptor agonist used for management of diabetes and obesity. It has been shown to be neuroprotective and to promote cell migration, but whether it can stimulate glial cells remains unknown. In the current study, we investigated the effects of liraglutide on OEC migration and explored the involved mechanisms. We showed that liraglutide at low concentration (100 nM) overall promoted OEC migration over time. Liraglutide modulated the migratory behavior of OECs by reducing time in arrest, and promoted random rather than straight migration. Liraglutide also induced a morphological change of primary OECs towards a bipolar shape consistent with improved migration. We found that liraglutide activated extracellular signal-regulated kinase (ERK), which has key roles in cell migration; the timing of ERK activation correlated with stimulation of migration. Furthermore, liraglutide also modulated the extracellular matrix by upregulating laminin-1 and down-regulating collagen IV. In summary, we found that liraglutide can stimulate OEC migration and re-model the extracellular matrix to better promote cell migration, and possibly also to become more conducive for axonal regeneration. Thus, liraglutide may improve OEC transplantation outcomes.
topic Glia
Extracellular signal-regulated kinase
Laminin-1
Collagen IV
GLP-1R
Cell transplantation
url http://www.sciencedirect.com/science/article/pii/S0753332221006016
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