Conditioned medium obtained from mesenchymal stem cells attenuates focal cerebral ischemia reperfusion injury through activation of ERK1/ERK2-BDNF signaling pathway.
Animals
Brain
/ drug effects
Brain Ischemia
/ metabolism
Brain-Derived Neurotrophic Factor
/ drug effects
Culture Media, Conditioned
/ pharmacology
Humans
MAP Kinase Signaling System
/ drug effects
Male
Mesenchymal Stem Cells
/ metabolism
Neurogenesis
/ drug effects
Neuroprotective Agents
/ pharmacology
Rats
Rats, Wistar
Reperfusion Injury
/ metabolism
BDNF
Conditioned medium
Mesenchymal stem cells
Neurogenesis
Phospho-ERK1/ERK2
Journal
Journal of chemical neuroanatomy
ISSN: 1873-6300
Titre abrégé: J Chem Neuroanat
Pays: Netherlands
ID NLM: 8902615
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
05
10
2018
revised:
13
02
2019
accepted:
17
02
2019
pubmed:
23
2
2019
medline:
27
6
2020
entrez:
22
2
2019
Statut:
ppublish
Résumé
Previous studies have shown that conditioned medium (CM) obtained from mesenchymal stem cells (MSCs) might exert neuroprotective effects against focal cerebral ischemia reperfusion (I/R) injury. This study was conducted to investigate if CM obtained from MSCs gives rise to neuroprotection by targeting neurogenesis. To induce focal cerebral ischemia in rats, middle cerebral artery (MCA) was occluded for 1 h and the amniotic mesenchymal stem cells-conditioned medium (AMSC-CM) at the dose of 0.5 μl was administered 30 min after reperfusion by stereotactic intracerebral infusion. The animals were randomly divided into three groups: sham operated animals received all procedures except occlusion of MCA (sham, n = 12), I/R group only received occlusion of MCA (MCAO, n = 17), treatment group received MCAO + 0.5 μl of AMSC-CM (MCAO + AMSC-CM, n = 17). The expression of Phospho-ERK1/ERK2, BDNF, VEGF and NGF were determined using immunohistochemical assay. Neuronal loss and DNA fragmentation were evaluated by Nissl and TUNEL assay, respectively. Our results demonstrated that the expression of Phospho-ERK1/ERK2 and BDNF, VEGF and NGF significantly decreased in MCAO rats and was reversed by AMSC-CM. Likewise, AMSC-CM markedly reduced neuronal loss and DNA fragmentation at 24 h after reperfusion. In sum, our study showed that AMSC-CM administration at the onset of reperfusion led to neuroprotection by activating neuronal ERK1/ERK2-BDNF signaling pathway, neurogenesis, angiogenesis as well as suppression of apoptosis.
Identifiants
pubmed: 30790626
pii: S0891-0618(18)30165-0
doi: 10.1016/j.jchemneu.2019.02.003
pii:
doi:
Substances chimiques
Brain-Derived Neurotrophic Factor
0
Culture Media, Conditioned
0
Neuroprotective Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
87-98Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.