Activation of Neurogenesis in Multipotent Stem Cells Cultured In Vitro and in the Spinal Cord Tissue After Severe Injury by Inhibition of Glycogen Synthase Kinase-3.


Journal

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
ISSN: 1878-7479
Titre abrégé: Neurotherapeutics
Pays: United States
ID NLM: 101290381

Informations de publication

Date de publication:
01 2021
Historique:
accepted: 01 09 2020
pubmed: 2 10 2020
medline: 15 12 2021
entrez: 1 10 2020
Statut: ppublish

Résumé

The inhibition of glycogen synthase kinase-3 (GSK-3) can induce neurogenesis, and the associated activation of Wnt/β-catenin signaling via GSK-3 inhibition may represent a means to promote motor function recovery following spinal cord injury (SCI) via increased astrocyte migration, reduced astrocyte apoptosis, and enhanced axonal growth. Herein, we assessed the effects of GSK-3 inhibition in vitro on the neurogenesis of ependymal stem/progenitor cells (epSPCs) resident in the mouse spinal cord and of human embryonic stem cell-derived neural progenitors (hESC-NPs) and human-induced pluripotent stem cell-derived neural progenitors (hiPSC-NPs) and in vivo on spinal cord tissue regeneration and motor activity after SCI. We report that the treatment of epSPCs and human pluripotent stem cell-derived neural progenitors (hPSC-NPs) with the GSK-3 inhibitor Ro3303544 activates β-catenin signaling and increases the expression of the bIII-tubulin neuronal marker; furthermore, the differentiation of Ro3303544-treated cells prompted an increase in the number of terminally differentiated neurons. Administration of a water-soluble, bioavailable form of this GSK-3 inhibitor (Ro3303544-Cl) in a severe SCI mouse model revealed the increased expression of bIII-tubulin in the injury epicenter. Treatment with Ro3303544-Cl increased survival of mature neuron types from the propriospinal tract (vGlut1, Parv) and raphe tract (5-HT), protein kinase C gamma-positive neurons, and GABAergic interneurons (GAD65/67) above the injury epicenter. Moreover, we observed higher numbers of newly born BrdU/DCX-positive neurons in Ro3303544-Cl-treated animal tissues, a reduced area delimited by astrocyte scar borders, and improved motor function. Based on this study, we believe that treating animals with epSPCs or hPSC-NPs in combination with Ro3303544-Cl deserves further investigation towards the development of a possible therapeutic strategy for SCI.

Identifiants

pubmed: 33000422
doi: 10.1007/s13311-020-00928-0
pii: 10.1007/s13311-020-00928-0
pmc: PMC8116371
doi:

Substances chimiques

Glycogen Synthase Kinase 3 EC 2.7.11.26

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

515-533

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Auteurs

Francisco Javier Rodriguez-Jimenez (FJ)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain.

Angel Vilches (A)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain.

Maria Amparo Perez-Arago (MA)

National Stem Cell Bank-Valencia Node, Biomolecular Resources Platform PRB3, ISCIII, Research Center "Principe Felipe", C/ Eduardo Primo Yúfera 3, 46012, Valencia, Spain.

Eleonora Clemente (E)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain.

Raquel Roman (R)

Organic Molecules Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, 46012, Valencia, Spain.
Department of Organic Chemistry, University of Valencia, 46100, Burjassot, Spain.

Juliette Leal (J)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain.

Ana Artero Castro (AA)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain.

Santos Fustero (S)

Organic Molecules Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, 46012, Valencia, Spain.
Department of Organic Chemistry, University of Valencia, 46100, Burjassot, Spain.

Victoria Moreno-Manzano (V)

Neuronal and Tissue Regeneration Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, 46012, Valencia, Spain.

Pavla Jendelova (P)

Institute of Experimental Medicine, Department of Neuroregeneration, Czech Academy of Sciences, Prague, Czech Republic.

Miodrag Stojkovic (M)

Department of Human Genetics, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.
Eaton Peabody Laboratories, Department of Otolaryngology, Massachusetts Eye and Ear, Boston, MA, USA.
Department of Otolaryngology-Head and Neck Surgery, Harvard Medical School, Boston, MA, USA.

Slaven Erceg (S)

Stem Cell Therapies in Neurodegenerative Diseases Lab, Research Center "Principe Felipe", C/ Eduardo Primo Yufera 3, Valencia, Spain. serceg@cipf.es.
National Stem Cell Bank-Valencia Node, Biomolecular Resources Platform PRB3, ISCIII, Research Center "Principe Felipe", C/ Eduardo Primo Yúfera 3, 46012, Valencia, Spain. serceg@cipf.es.
Institute of Experimental Medicine, Department of Neuroregeneration, Czech Academy of Sciences, Prague, Czech Republic. serceg@cipf.es.

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