Cargando…

Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death

BACKGROUND: The paracrine effect is likely the major mechanism of the adipose-derived stem cell (ASC)-mediated cardioprotective effect. However, the exact composition and nature of ASC-released paracrine factors remain elusive. In the present study, we examined the effect of osteoprotegerin (OPG), a...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Jiyun, Lee, Seahyung, Lee, Chang Youn, Seo, Hyang-Hee, Shin, Sunhye, Choi, Jung-Won, Kim, Sang Woo, Park, Jong-Chul, Lim, Soyeon, Hwang, Ki-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606035/
https://www.ncbi.nlm.nih.gov/pubmed/28931423
http://dx.doi.org/10.1186/s13287-017-0647-6
_version_ 1783265088843546624
author Lee, Jiyun
Lee, Seahyung
Lee, Chang Youn
Seo, Hyang-Hee
Shin, Sunhye
Choi, Jung-Won
Kim, Sang Woo
Park, Jong-Chul
Lim, Soyeon
Hwang, Ki-Chul
author_facet Lee, Jiyun
Lee, Seahyung
Lee, Chang Youn
Seo, Hyang-Hee
Shin, Sunhye
Choi, Jung-Won
Kim, Sang Woo
Park, Jong-Chul
Lim, Soyeon
Hwang, Ki-Chul
author_sort Lee, Jiyun
collection PubMed
description BACKGROUND: The paracrine effect is likely the major mechanism of the adipose-derived stem cell (ASC)-mediated cardioprotective effect. However, the exact composition and nature of ASC-released paracrine factors remain elusive. In the present study, we examined the effect of osteoprotegerin (OPG), a stem cell-released decoy receptor for death ligand, on the survival of cardiomyocytes exposed to oxidative stress. METHODS: The production of OPG from ASCs under oxidative stress was determined by ELISA and immunohistochemistry. The effects of OPG and the OPG-containing conditioned media of ASCs on the survival of cardiomyocytes were determined using a cell viability assay. RESULTS: Hydrogen peroxide (H(2)O(2)) significantly increased OPG production from ASCs in vitro, and OPG production from the ASCs transplanted into the ischemia–reperfusion-injured heart was also observed. OPG significantly attenuated cardiomyocyte death in vitro. OPG-containing conditioned media of ASCs also significantly protected cardiomyocytes. Delivery of siRNA specific to OPG significantly decreased the OPG production of ASCs, and also offset the protective effect of the conditioned media of ASCs. CONCLUSIONS: Our study strongly suggests that OPG is one of the prosurvival factors released from ASCs that may contribute to the ASC-mediated cardioprotection and calls for further studies to elucidate detailed underlying mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0647-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5606035
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-56060352017-09-20 Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death Lee, Jiyun Lee, Seahyung Lee, Chang Youn Seo, Hyang-Hee Shin, Sunhye Choi, Jung-Won Kim, Sang Woo Park, Jong-Chul Lim, Soyeon Hwang, Ki-Chul Stem Cell Res Ther Short Report BACKGROUND: The paracrine effect is likely the major mechanism of the adipose-derived stem cell (ASC)-mediated cardioprotective effect. However, the exact composition and nature of ASC-released paracrine factors remain elusive. In the present study, we examined the effect of osteoprotegerin (OPG), a stem cell-released decoy receptor for death ligand, on the survival of cardiomyocytes exposed to oxidative stress. METHODS: The production of OPG from ASCs under oxidative stress was determined by ELISA and immunohistochemistry. The effects of OPG and the OPG-containing conditioned media of ASCs on the survival of cardiomyocytes were determined using a cell viability assay. RESULTS: Hydrogen peroxide (H(2)O(2)) significantly increased OPG production from ASCs in vitro, and OPG production from the ASCs transplanted into the ischemia–reperfusion-injured heart was also observed. OPG significantly attenuated cardiomyocyte death in vitro. OPG-containing conditioned media of ASCs also significantly protected cardiomyocytes. Delivery of siRNA specific to OPG significantly decreased the OPG production of ASCs, and also offset the protective effect of the conditioned media of ASCs. CONCLUSIONS: Our study strongly suggests that OPG is one of the prosurvival factors released from ASCs that may contribute to the ASC-mediated cardioprotection and calls for further studies to elucidate detailed underlying mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0647-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-19 /pmc/articles/PMC5606035/ /pubmed/28931423 http://dx.doi.org/10.1186/s13287-017-0647-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Lee, Jiyun
Lee, Seahyung
Lee, Chang Youn
Seo, Hyang-Hee
Shin, Sunhye
Choi, Jung-Won
Kim, Sang Woo
Park, Jong-Chul
Lim, Soyeon
Hwang, Ki-Chul
Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title_full Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title_fullStr Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title_full_unstemmed Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title_short Adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
title_sort adipose-derived stem cell-released osteoprotegerin protects cardiomyocytes from reactive oxygen species-induced cell death
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606035/
https://www.ncbi.nlm.nih.gov/pubmed/28931423
http://dx.doi.org/10.1186/s13287-017-0647-6
work_keys_str_mv AT leejiyun adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT leeseahyung adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT leechangyoun adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT seohyanghee adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT shinsunhye adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT choijungwon adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT kimsangwoo adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT parkjongchul adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT limsoyeon adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath
AT hwangkichul adiposederivedstemcellreleasedosteoprotegerinprotectscardiomyocytesfromreactiveoxygenspeciesinducedcelldeath