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  4. Neonatal Mesenchymal Stem Cell Treatment Improves Myelination Impaired by Global Perinatal Asphyxia in Rats
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Neonatal Mesenchymal Stem Cell Treatment Improves Myelination Impaired by Global Perinatal Asphyxia in Rats

Journal
International Journal of Molecular Sciences
ISSN
1422-0067
Date Issued
2021
Author(s)
Andrea Tapia-Bustos
Carolyne Lespay-Rebolledo
Valentina Vío
Ronald Pérez-Lobos
Emmanuel Casanova-Ortiz
EZQUER, EDUARDO FERNANDO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Mario Herrera-Marschitz
Paola Morales
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85102795463
WoS ID
WOS:000645786800001
DOI
10.3390/ijms22063275
URL
https://investigadores.udd.cl/handle/123456789/6525
URL Institutional Repository
http://hdl.handle.net/11447/5692
Abstract
<jats:p>The effect of perinatal asphyxia (PA) on oligodendrocyte (OL), neuroinflammation, and cell viability was evaluated in telencephalon of rats at postnatal day (P)1, 7, and 14, a period characterized by a spur of neuronal networking, evaluating the effect of mesenchymal stem cell (MSCs)-treatment. The issue was investigated with a rat model of global PA, mimicking a clinical risk occurring under labor. PA was induced by immersing fetus-containing uterine horns into a water bath for 21 min (AS), using sibling-caesarean-delivered fetuses (CS) as controls. Two hours after delivery, AS and CS neonates were injected with either 5 μL of vehicle (10% plasma) or 5 × 104 MSCs into the lateral ventricle. Samples were assayed for myelin-basic protein (MBP) levels; Olig-1/Olig-2 transcriptional factors; Gglial phenotype; neuroinflammation, and delayed cell death. The main effects were observed at P7, including: (i) A decrease of MBP-immunoreactivity in external capsule, corpus callosum, cingulum, but not in fimbriae of hippocampus; (ii) an increase of Olig-1-mRNA levels; (iii) an increase of IL-6-mRNA, but not in protein levels; (iv) an increase in cell death, including OLs; and (v) MSCs treatment prevented the effect of PA on myelination, OLs number, and cell death. The present findings show that PA induces regional- and developmental-dependent changes on myelination and OLs maturation. Neonatal MSCs treatment improves survival of mature OLs and myelination in telencephalic white matter.</jats:p>
Cite this document
Tapia-Bustos, A., Lespay-Rebolledo, C., Vío, V., Pérez-Lobos, R., Casanova-Ortiz, E., Ezquer, F., Herrera-Marschitz, M., & Morales, P. (2021). Neonatal mesenchymal stem cell treatment improves myelination impaired by global perinatal asphyxia in rats. International Journal of Molecular Sciences, 22(6), 3275. https://doi.org/10.3390/ijms22063275
Project(s)
Treating the whole not the hole: Administration of acellular derivative from mesenchymal stem cells subjected to a preconditioning stimulus reverts diabetic neuropathy and prevents diabetic foot ulcers in an animal model of type 2 diabetes mellitus  
Mesenchymal stem cells-secretome provides protection in neonatal hypoxiareoxygenation. Mechanisms and translational studies  
Subjects
hypomyelination

; 

oligodendrocyte

; 

myelination

; 

neonatal asphyxia

; 

ischemia

; 

apoptosis

; 

mesenchymal stem cells

; 

telencephalon

; 

rat brain

; 

neuroinflammation

; 

periventricular leukomalacia

; 

animals

; 

animals, newborn

; 

apgar score

; 

asphyxia

; 

biomarkers

; 

brain

; 

cell differentiation

; 

cell survival

; 

cytokines

; 

gene expression

; 

hippocampus

; 

immunohistochemistry

; 

inflammation mediators

; 

mesenchymal stem cell transplantation

; 

mesenchymal stem cells

; 

myelin sheath

; 

neuroglia

; 

oligodendroglia

; 

rats

; 

rna, messenger

; 

interleukin 6

; 

messenger rna

; 

myelin basic protein

; 

oligodendrocyte transcription factor 2

; 

autacoid

; 

biological marker

; 

cytokine

; 

messenger rna

; 

animal cell

; 

animal experiment

; 

animal model

; 

animal tissue

; 

article

; 

brain lateral ventricle

; 

breathing rate

; 

cell maturation

; 

cell viability

; 

cingulum (brain)

; 

confocal microscopy

; 

controlled study

; 

corpus callosum

; 

external capsule

; 

female

; 

fetus

; 

hippocampal fimbria

; 

immunoreactivity

; 

mesenchymal stem cell transplantation

; 

mrna expression level

; 

myelinated nerve

; 

myelination

; 

nervous system inflammation

; 

neuroprotection

; 

newborn

; 

nonhuman

; 

oligodendroglia

; 

perinatal asphyxia

; 

perinatal development

; 

protein expression level

; 

rat

; 

survival rate

; 

telencephalon

; 

uterus horn

; 

animal

; 

apgar score

; 

asphyxia

; 

brain

; 

cell differentiation

; 

cell survival

; 

cytology

; 

gene expression

; 

genetics

; 

glia

; 

hippocampus

; 

immunohistochemistry

; 

immunology

; 

mesenchymal stem cell

; 

metabolism

; 

myelin sheath

; 

oligodendroglia

; 

pathology
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