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Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells

One of the readily available sources of mesenchymal stem cells (MSCs) is menstrual blood-derived stem cells (Men-SCs), which exhibit characteristics similar to other types of MSCs. This study was performed to determine the growth kinetics, plasticity, and characterization of Men-SCs in women. During...

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Autores principales: Mehrabani, Davood, Nazarabadi, Roshanak Bahrami, Kasraeian, Maryam, Tamadon, Amin, Dianatpour, Mehdi, Vahdati, Akbar, Zare, Shahrokh, Ghobadi, Farnaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Journal of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764963/
https://www.ncbi.nlm.nih.gov/pubmed/26989284
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author Mehrabani, Davood
Nazarabadi, Roshanak Bahrami
Kasraeian, Maryam
Tamadon, Amin
Dianatpour, Mehdi
Vahdati, Akbar
Zare, Shahrokh
Ghobadi, Farnaz
author_facet Mehrabani, Davood
Nazarabadi, Roshanak Bahrami
Kasraeian, Maryam
Tamadon, Amin
Dianatpour, Mehdi
Vahdati, Akbar
Zare, Shahrokh
Ghobadi, Farnaz
author_sort Mehrabani, Davood
collection PubMed
description One of the readily available sources of mesenchymal stem cells (MSCs) is menstrual blood-derived stem cells (Men-SCs), which exhibit characteristics similar to other types of MSCs. This study was performed to determine the growth kinetics, plasticity, and characterization of Men-SCs in women. During spring 2014 in the southern Iranian city of Shiraz, menstrual blood (5 mL) was obtained from 10 women on their third day of menstruation in 2 age groups of 30 to 40 and 40 to 50 years old. Ficoll was used to separate the mononuclear cell fraction. After the Men-SCs were cultured, they were subcultured up to passage 4. Growth behavior and population doubling time were evaluated by seeding 5×10(4) cells into 12- and 24-well culture plates, and the colonies were enumerated. The expression of CD44, CD90, and CD34 was evaluated. The osteogenic potential was assessed by alizarin red staining. The Men-SCs were shown to be plastic adherent and spindle-shaped. Regarding the growth curves in the 12- and 24-well culture plates, it was demonstrated that in the women aged between 30 and 40 years, population doubling time was 55.5 and 62 hours, respectively, while these values in the women aged between 40 and 50 years were 70.4 and 72.4 hours, correspondingly. Positive expression of CD44 and CD90 and negative expression of CD34 were noted. In the osteogenic differentiation medium, the cells differentiated toward osteoblasts. As human Men-SCs are easily collectable without any invasive procedure and are a safe and rapid source of MSCs, they can be a good candidate for stem cell banking and cell transplantation in women.
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spelling pubmed-47649632016-03-17 Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells Mehrabani, Davood Nazarabadi, Roshanak Bahrami Kasraeian, Maryam Tamadon, Amin Dianatpour, Mehdi Vahdati, Akbar Zare, Shahrokh Ghobadi, Farnaz Iran J Med Sci Brief Report One of the readily available sources of mesenchymal stem cells (MSCs) is menstrual blood-derived stem cells (Men-SCs), which exhibit characteristics similar to other types of MSCs. This study was performed to determine the growth kinetics, plasticity, and characterization of Men-SCs in women. During spring 2014 in the southern Iranian city of Shiraz, menstrual blood (5 mL) was obtained from 10 women on their third day of menstruation in 2 age groups of 30 to 40 and 40 to 50 years old. Ficoll was used to separate the mononuclear cell fraction. After the Men-SCs were cultured, they were subcultured up to passage 4. Growth behavior and population doubling time were evaluated by seeding 5×10(4) cells into 12- and 24-well culture plates, and the colonies were enumerated. The expression of CD44, CD90, and CD34 was evaluated. The osteogenic potential was assessed by alizarin red staining. The Men-SCs were shown to be plastic adherent and spindle-shaped. Regarding the growth curves in the 12- and 24-well culture plates, it was demonstrated that in the women aged between 30 and 40 years, population doubling time was 55.5 and 62 hours, respectively, while these values in the women aged between 40 and 50 years were 70.4 and 72.4 hours, correspondingly. Positive expression of CD44 and CD90 and negative expression of CD34 were noted. In the osteogenic differentiation medium, the cells differentiated toward osteoblasts. As human Men-SCs are easily collectable without any invasive procedure and are a safe and rapid source of MSCs, they can be a good candidate for stem cell banking and cell transplantation in women. Iranian Journal of Medical Sciences 2016-03 /pmc/articles/PMC4764963/ /pubmed/26989284 Text en Copyright: © Iranian Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Mehrabani, Davood
Nazarabadi, Roshanak Bahrami
Kasraeian, Maryam
Tamadon, Amin
Dianatpour, Mehdi
Vahdati, Akbar
Zare, Shahrokh
Ghobadi, Farnaz
Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title_full Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title_fullStr Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title_full_unstemmed Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title_short Growth Kinetics, Characterization, and Plasticity of Human Menstrual Blood Stem Cells
title_sort growth kinetics, characterization, and plasticity of human menstrual blood stem cells
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764963/
https://www.ncbi.nlm.nih.gov/pubmed/26989284
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