Cargando…

Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect

Oxidative stress induces damages of various cell types or tissues through a repetitive imbalance between the systemic manifestation of reactive oxygen species (ROS) and detoxification of the reactive intermediates. Thioacetamide (TAA) is well known for causing several degenerative diseases by oxidat...

Descripción completa

Detalles Bibliográficos
Autores principales: Na, Jeeyoon, Song, Joseph, Kim, Hyun Ho, Seok, Jin, Kim, Jae Yeon, Jun, Ji Hye, Kim, Gi Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835021/
https://www.ncbi.nlm.nih.gov/pubmed/33406506
http://dx.doi.org/10.18632/aging.202348
_version_ 1783642421531246592
author Na, Jeeyoon
Song, Joseph
Kim, Hyun Ho
Seok, Jin
Kim, Jae Yeon
Jun, Ji Hye
Kim, Gi Jin
author_facet Na, Jeeyoon
Song, Joseph
Kim, Hyun Ho
Seok, Jin
Kim, Jae Yeon
Jun, Ji Hye
Kim, Gi Jin
author_sort Na, Jeeyoon
collection PubMed
description Oxidative stress induces damages of various cell types or tissues through a repetitive imbalance between the systemic manifestation of reactive oxygen species (ROS) and detoxification of the reactive intermediates. Thioacetamide (TAA) is well known for causing several degenerative diseases by oxidative stress. However, study of the antioxidant mechanisms of stem cells in TAA-injured rat model is insufficient. Therefore, we investigated the effect of placenta-derived mesenchymal stem cells (PD-MSCs) transplantation on liver and ovary of TAA-injured rat models to study the antioxidant effect in degenerative diseases. In TAA-injured rat model, PD-MSCs engrafted into damaged organ including liver and ovary in PD-MSCs transplanted groups (Tx) compared with non-transplanted groups (NTx) (*p<0.05). Transplanted PD-MSCs reduced inflammatory factors and upregulated oxidative stress factors in Tx compared with NTx (*p<0.05). Also, transplanted PD-MSCs enhanced antioxidants factors and organ functional restoration factors in Tx compared with NTx. These data show that PD-MSC transplantation triggers the regeneration of organ (e.g., liver and ovary) damaged by oxidative stress from TAA treatment via activating antioxidant factors. Therefore, these data suggest the therapeutic potential via antioxidant effect and help understand the therapeutic mechanism of PD-MSCs in damaged tissues such as in liver and reproductive system.
format Online
Article
Text
id pubmed-7835021
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Impact Journals
record_format MEDLINE/PubMed
spelling pubmed-78350212021-02-03 Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect Na, Jeeyoon Song, Joseph Kim, Hyun Ho Seok, Jin Kim, Jae Yeon Jun, Ji Hye Kim, Gi Jin Aging (Albany NY) Research Paper Oxidative stress induces damages of various cell types or tissues through a repetitive imbalance between the systemic manifestation of reactive oxygen species (ROS) and detoxification of the reactive intermediates. Thioacetamide (TAA) is well known for causing several degenerative diseases by oxidative stress. However, study of the antioxidant mechanisms of stem cells in TAA-injured rat model is insufficient. Therefore, we investigated the effect of placenta-derived mesenchymal stem cells (PD-MSCs) transplantation on liver and ovary of TAA-injured rat models to study the antioxidant effect in degenerative diseases. In TAA-injured rat model, PD-MSCs engrafted into damaged organ including liver and ovary in PD-MSCs transplanted groups (Tx) compared with non-transplanted groups (NTx) (*p<0.05). Transplanted PD-MSCs reduced inflammatory factors and upregulated oxidative stress factors in Tx compared with NTx (*p<0.05). Also, transplanted PD-MSCs enhanced antioxidants factors and organ functional restoration factors in Tx compared with NTx. These data show that PD-MSC transplantation triggers the regeneration of organ (e.g., liver and ovary) damaged by oxidative stress from TAA treatment via activating antioxidant factors. Therefore, these data suggest the therapeutic potential via antioxidant effect and help understand the therapeutic mechanism of PD-MSCs in damaged tissues such as in liver and reproductive system. Impact Journals 2020-12-26 /pmc/articles/PMC7835021/ /pubmed/33406506 http://dx.doi.org/10.18632/aging.202348 Text en Copyright: © 2020 Na et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Na, Jeeyoon
Song, Joseph
Kim, Hyun Ho
Seok, Jin
Kim, Jae Yeon
Jun, Ji Hye
Kim, Gi Jin
Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title_full Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title_fullStr Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title_full_unstemmed Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title_short Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect
title_sort human placenta-derived mesenchymal stem cells trigger repair system in taa-injured rat model via antioxidant effect
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835021/
https://www.ncbi.nlm.nih.gov/pubmed/33406506
http://dx.doi.org/10.18632/aging.202348
work_keys_str_mv AT najeeyoon humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT songjoseph humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT kimhyunho humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT seokjin humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT kimjaeyeon humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT junjihye humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect
AT kimgijin humanplacentaderivedmesenchymalstemcellstriggerrepairsystemintaainjuredratmodelviaantioxidanteffect