Mitochondrial dynamics and sex-specific responses in the developing rat hippocampus: Effect of perinatal asphyxia and mesenchymal stem cell Secretome treatment

Perinatal asphyxia is one of the major causes of neonatal death at birth. Survivors can progress but often suffer from long-term sequelae. We aim to determine the effects of perinatal asphyxia on mitochondrial dynamics and whether mesenchymal stem cell secretome (MSC-S) treatment can alleviate the d...

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Veröffentlicht in:Biochimica et biophysica acta. Molecular cell research 2024-12, Vol.1871 (8), p.119851, Article 119851
Hauptverfasser: Zamorano-Cataldo, M., Vega-Vásquez, I., García-Navarrete, C., Toledo, J., Bustamante, D., Ezquer, F., Urra, F.A., Farfán-Troncoso, N., Herrera-Marschitz, M., Morales, P.
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container_issue 8
container_start_page 119851
container_title Biochimica et biophysica acta. Molecular cell research
container_volume 1871
creator Zamorano-Cataldo, M.
Vega-Vásquez, I.
García-Navarrete, C.
Toledo, J.
Bustamante, D.
Ezquer, F.
Urra, F.A.
Farfán-Troncoso, N.
Herrera-Marschitz, M.
Morales, P.
description Perinatal asphyxia is one of the major causes of neonatal death at birth. Survivors can progress but often suffer from long-term sequelae. We aim to determine the effects of perinatal asphyxia on mitochondrial dynamics and whether mesenchymal stem cell secretome (MSC-S) treatment can alleviate the deleterious effects. Animals were subjected to 21 min of asphyxia at the time of delivery. MSC-S or vehicle was intranasally administered 2 h post-delivery. Mitochondrial mass (D-loop, qPCR), mitochondrial dynamics proteins (Drp1, Fis1 and OPA1, Western blot), mitochondrial dynamics (TOMM20, Immunofluorescence), as well as mitochondrial membrane potential (ΔΨm) (Safranin O) were evaluated at P1 and P7 in the hippocampus. Perinatal asphyxia increased levels of mitochondrial dynamics proteins Drp1 and S-OPA1 at P1 and Fis1 at P7. Mitochondrial density and mass were decreased at P1. Perinatal asphyxia induced sex-specific differences, with increased L-OPA1 in females at P7 and increased mitochondria circularity. In males, asphyxia-exposed animals exhibited a reduced ΔΨm at P7. MSC-S treatment normalised levels of mitochondrial dynamics proteins involved in fission. This study provides novel insights into the effects of perinatal asphyxia on mitochondrial dynamics in the developing brain and on the therapeutic opportunities provided by mesenchymal stem cell secretome treatment. It also highlights on the relevance of considering sex as a biological variable in perinatal brain injury and therapy development. These findings contribute to the development of targeted, personalised therapies for infants affected by perinatal asphyxia. •This study provides novel insights into the effects of perinatal asphyxia on mitochondrial dynamics in the developing brain.•It explores the therapeutic benefits of mesenchymal stem cell (MSC) secretome treatment for mitigating PA-induced damage.•It highlights on the relevance of sex as a biological variable for undesrtanding perinatal brain injury and treatment.•The findings contribute to the development of targeted personalised treatment for infants affected by perinatal asphyxia.
doi_str_mv 10.1016/j.bbamcr.2024.119851
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Survivors can progress but often suffer from long-term sequelae. We aim to determine the effects of perinatal asphyxia on mitochondrial dynamics and whether mesenchymal stem cell secretome (MSC-S) treatment can alleviate the deleterious effects. Animals were subjected to 21 min of asphyxia at the time of delivery. MSC-S or vehicle was intranasally administered 2 h post-delivery. Mitochondrial mass (D-loop, qPCR), mitochondrial dynamics proteins (Drp1, Fis1 and OPA1, Western blot), mitochondrial dynamics (TOMM20, Immunofluorescence), as well as mitochondrial membrane potential (ΔΨm) (Safranin O) were evaluated at P1 and P7 in the hippocampus. Perinatal asphyxia increased levels of mitochondrial dynamics proteins Drp1 and S-OPA1 at P1 and Fis1 at P7. Mitochondrial density and mass were decreased at P1. Perinatal asphyxia induced sex-specific differences, with increased L-OPA1 in females at P7 and increased mitochondria circularity. 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subjects Development
Hippocampus
Mesenchymal stem cell secretome
Mitochondrial dynamics
Perinatal asphyxia
Sex differences
title Mitochondrial dynamics and sex-specific responses in the developing rat hippocampus: Effect of perinatal asphyxia and mesenchymal stem cell Secretome treatment
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