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Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study

BACKGROUND: Human endometrium with consecutive regeneration capability undergoes monthly hormonal changes for probable implantation, which confirms the presence of the cells in the basalis layer known as stem cell. OBJECTIVE: Previously, we reported the isolation and culture of the mesenchymal-like...

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Autores principales: Akyash, Fatemeh, Javidpou, Mahdieh, Yazd, Ehsan Farashahi, Golzadeh, Jalal, Hajizadeh-Tafti, Fatemeh, Aflatoonian, Reza, Aflatoonian, Behrouz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749975/
https://www.ncbi.nlm.nih.gov/pubmed/33349802
http://dx.doi.org/10.18502/ijrm.v13i11.7961
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author Akyash, Fatemeh
Javidpou, Mahdieh
Yazd, Ehsan Farashahi
Golzadeh, Jalal
Hajizadeh-Tafti, Fatemeh
Aflatoonian, Reza
Aflatoonian, Behrouz
author_facet Akyash, Fatemeh
Javidpou, Mahdieh
Yazd, Ehsan Farashahi
Golzadeh, Jalal
Hajizadeh-Tafti, Fatemeh
Aflatoonian, Reza
Aflatoonian, Behrouz
author_sort Akyash, Fatemeh
collection PubMed
description BACKGROUND: Human endometrium with consecutive regeneration capability undergoes monthly hormonal changes for probable implantation, which confirms the presence of the cells in the basalis layer known as stem cell. OBJECTIVE: Previously, we reported the isolation and culture of the mesenchymal-like cells from human endometrium. In this study, we evaluated the biological and stemness characteristics of these cells. MATERIALS AND METHODS: The characterization of Yazd human endometrial-derived mesenchymal stem/stromal cells (YhEnMSCs) was assessed using immunofluorescence (IF) staining for CD105, VIMENTIN, and FIBRONECTIN as markers and RT-PCR for CD166, CD10, CD105, VIMENTIN, FIBRONECTIN, MHCI, CD14, and MHCII genes. Flow cytometry (FACS) was performed for CD44, CD73, CD90, and CD105 markers. Moreover, the differentiation capacity of the YhEnMSCs to the osteoblast and adipocytes was confirmed by Alizarin Red and Oil Red staining. RESULTS: YhEnMSCs expressed CD105, VIMENTIN, FIBRONECTIN, CD44, CD73, and CD90 markers and CD166, CD10, CD105, VIMENTIN, FIBRONECTIN, and MHCI, but, did not express CD14, MHCII. CONCLUSION: Our data confirm previous reports by other groups indicating the application of endometrial cells as an available source of MSCs with self-renewal and differentiation capacity. Accordingly, YhEnMSCs can be used as a suitable source for cell-based therapies.
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spelling pubmed-77499752020-12-20 Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study Akyash, Fatemeh Javidpou, Mahdieh Yazd, Ehsan Farashahi Golzadeh, Jalal Hajizadeh-Tafti, Fatemeh Aflatoonian, Reza Aflatoonian, Behrouz Int J Reprod Biomed Research Article BACKGROUND: Human endometrium with consecutive regeneration capability undergoes monthly hormonal changes for probable implantation, which confirms the presence of the cells in the basalis layer known as stem cell. OBJECTIVE: Previously, we reported the isolation and culture of the mesenchymal-like cells from human endometrium. In this study, we evaluated the biological and stemness characteristics of these cells. MATERIALS AND METHODS: The characterization of Yazd human endometrial-derived mesenchymal stem/stromal cells (YhEnMSCs) was assessed using immunofluorescence (IF) staining for CD105, VIMENTIN, and FIBRONECTIN as markers and RT-PCR for CD166, CD10, CD105, VIMENTIN, FIBRONECTIN, MHCI, CD14, and MHCII genes. Flow cytometry (FACS) was performed for CD44, CD73, CD90, and CD105 markers. Moreover, the differentiation capacity of the YhEnMSCs to the osteoblast and adipocytes was confirmed by Alizarin Red and Oil Red staining. RESULTS: YhEnMSCs expressed CD105, VIMENTIN, FIBRONECTIN, CD44, CD73, and CD90 markers and CD166, CD10, CD105, VIMENTIN, FIBRONECTIN, and MHCI, but, did not express CD14, MHCII. CONCLUSION: Our data confirm previous reports by other groups indicating the application of endometrial cells as an available source of MSCs with self-renewal and differentiation capacity. Accordingly, YhEnMSCs can be used as a suitable source for cell-based therapies. Knowledge E 2020-11-22 /pmc/articles/PMC7749975/ /pubmed/33349802 http://dx.doi.org/10.18502/ijrm.v13i11.7961 Text en Copyright © 2020 Akyash et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Article
Akyash, Fatemeh
Javidpou, Mahdieh
Yazd, Ehsan Farashahi
Golzadeh, Jalal
Hajizadeh-Tafti, Fatemeh
Aflatoonian, Reza
Aflatoonian, Behrouz
Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title_full Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title_fullStr Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title_full_unstemmed Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title_short Characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: A lab resources study
title_sort characteristics of the human endometrial regeneration cells as a potential source for future stem cell-based therapies: a lab resources study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749975/
https://www.ncbi.nlm.nih.gov/pubmed/33349802
http://dx.doi.org/10.18502/ijrm.v13i11.7961
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