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Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium

BACKGROUND: Asherman’s syndrome (AS) is one of the gynecological disorders caused by the destruction of the endometrium. For some cases of AS available surgical methods and hormonal therapy are ineffective. Stem cell transplantation may offer a potential alternative for AS cure. METHODS: Human endom...

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Autores principales: Domnina, Alisa, Novikova, Polina, Obidina, Julia, Fridlyanskaya, Irina, Alekseenko, Larisa, Kozhukharova, Irina, Lyublinskaya, Olga, Zenin, Valeriy, Nikolsky, Nikolay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828181/
https://www.ncbi.nlm.nih.gov/pubmed/29482664
http://dx.doi.org/10.1186/s13287-018-0801-9
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author Domnina, Alisa
Novikova, Polina
Obidina, Julia
Fridlyanskaya, Irina
Alekseenko, Larisa
Kozhukharova, Irina
Lyublinskaya, Olga
Zenin, Valeriy
Nikolsky, Nikolay
author_facet Domnina, Alisa
Novikova, Polina
Obidina, Julia
Fridlyanskaya, Irina
Alekseenko, Larisa
Kozhukharova, Irina
Lyublinskaya, Olga
Zenin, Valeriy
Nikolsky, Nikolay
author_sort Domnina, Alisa
collection PubMed
description BACKGROUND: Asherman’s syndrome (AS) is one of the gynecological disorders caused by the destruction of the endometrium. For some cases of AS available surgical methods and hormonal therapy are ineffective. Stem cell transplantation may offer a potential alternative for AS cure. METHODS: Human endometrial mesenchymal stem cells (eMSC) organized in spheroids were transplanted in rats with damaged endometrium modeled on AS. Treatment response was defined as pregnancy outcome and litter size. RESULTS: Application of eMSC in spheroids significantly improved the rat fertility with the AS model. eMSC organized in spheroids retain all properties of eMSC in monolayer: growth characteristics, expression of CD markers, and differentiation potential. Synthesis of angiogenic and anti-inflammatory factors drastically increased in eMSC assembled into spheroids. CONCLUSIONS: Human endometrial mesenchymal stem cells (eMSC) can be successfully applied for Asherman’s syndrome (AS) treatment in the rat model. eMSC organized in spheroids were more therapeutically effective than the cells in monolayer. After transplantation of eMSC in spheroids the pregnancy outcome and litter size in rats with AS was higher than in rats that received autologous rat bone marrow cells. It suggests the therapeutic plausibility of heterologous eMSC in case of failure to use autologous cells.
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spelling pubmed-58281812018-02-28 Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium Domnina, Alisa Novikova, Polina Obidina, Julia Fridlyanskaya, Irina Alekseenko, Larisa Kozhukharova, Irina Lyublinskaya, Olga Zenin, Valeriy Nikolsky, Nikolay Stem Cell Res Ther Research BACKGROUND: Asherman’s syndrome (AS) is one of the gynecological disorders caused by the destruction of the endometrium. For some cases of AS available surgical methods and hormonal therapy are ineffective. Stem cell transplantation may offer a potential alternative for AS cure. METHODS: Human endometrial mesenchymal stem cells (eMSC) organized in spheroids were transplanted in rats with damaged endometrium modeled on AS. Treatment response was defined as pregnancy outcome and litter size. RESULTS: Application of eMSC in spheroids significantly improved the rat fertility with the AS model. eMSC organized in spheroids retain all properties of eMSC in monolayer: growth characteristics, expression of CD markers, and differentiation potential. Synthesis of angiogenic and anti-inflammatory factors drastically increased in eMSC assembled into spheroids. CONCLUSIONS: Human endometrial mesenchymal stem cells (eMSC) can be successfully applied for Asherman’s syndrome (AS) treatment in the rat model. eMSC organized in spheroids were more therapeutically effective than the cells in monolayer. After transplantation of eMSC in spheroids the pregnancy outcome and litter size in rats with AS was higher than in rats that received autologous rat bone marrow cells. It suggests the therapeutic plausibility of heterologous eMSC in case of failure to use autologous cells. BioMed Central 2018-02-26 /pmc/articles/PMC5828181/ /pubmed/29482664 http://dx.doi.org/10.1186/s13287-018-0801-9 Text en © The Author(s). 2018 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 Research
Domnina, Alisa
Novikova, Polina
Obidina, Julia
Fridlyanskaya, Irina
Alekseenko, Larisa
Kozhukharova, Irina
Lyublinskaya, Olga
Zenin, Valeriy
Nikolsky, Nikolay
Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title_full Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title_fullStr Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title_full_unstemmed Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title_short Human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
title_sort human mesenchymal stem cells in spheroids improve fertility in model animals with damaged endometrium
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828181/
https://www.ncbi.nlm.nih.gov/pubmed/29482664
http://dx.doi.org/10.1186/s13287-018-0801-9
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