Conditioned medium obtained from mesenchymal stem cells attenuates focal cerebral ischemia reperfusion injury through activation of ERK1/ERK2-BDNF signaling pathway.


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
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

87-98

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Nahid Aboutaleb (N)

Physiology Research Center and Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran. Electronic address: dr_nabo40@yahoo.com.

Masoumeh Faezi (M)

Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Solmaz Nasseri Maleki (S)

Physiology Research Center and Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Donya Nazarinia (D)

Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Seyed Mohammad Taghi Razavi Tousi (SMT)

Medical Biotechnology Research Center, Guilan University of Medical Sciences, Rasht, Iran.

Narjes Hashemirad (N)

Department of biology science, Damghan University of Basic Sciences, Damghan, Semnan, Iran.

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Classifications MeSH