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Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome
Secretome of multipotent mesenchymal stromal cells (MSCs) is actively used in biomedical applications such as alveolar bone regeneration, treatment of cardiovascular disease, and neurodegenerative disorders. Nevertheless, hMSCs have low proliferative potential and production of the industrial quanti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716221/ https://www.ncbi.nlm.nih.gov/pubmed/33198321 http://dx.doi.org/10.3390/molecules25225283 |
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author | Lobov, Arseniy A. Yudintceva, Natalia M. Mittenberg, Alexey G. Shabelnikov, Sergey V. Mikhailova, Natalia A. Malashicheva, Anna B. Khotin, Mikhail G. |
author_facet | Lobov, Arseniy A. Yudintceva, Natalia M. Mittenberg, Alexey G. Shabelnikov, Sergey V. Mikhailova, Natalia A. Malashicheva, Anna B. Khotin, Mikhail G. |
author_sort | Lobov, Arseniy A. |
collection | PubMed |
description | Secretome of multipotent mesenchymal stromal cells (MSCs) is actively used in biomedical applications such as alveolar bone regeneration, treatment of cardiovascular disease, and neurodegenerative disorders. Nevertheless, hMSCs have low proliferative potential and production of the industrial quantity of their secretome might be challenging. Human fetal multipotent mesenchymal stromal cells (FetMSCs) isolated from early human embryo bone marrow are easy to expand and might be a potential source for pharmaceutical substances production based on their secretome. However, the secretome of FetMSCs was not previously analyzed. Here, we describe the secretome of FetMSCs using LC-MALDI shotgun proteomics. We identified 236 proteins. Functional annotation of the identified proteins revealed their involvement in angiogenesis, ossification, regulation of apoptosis, and immune response processes, which made it promising for biomedical applications. The proteins identified in the FetMSCs secretome are involved in the same biological processes as proteins from previously described adult hMSCs secretomes. Nevertheless, many of the common hMSCs secretome components (such as VEGF, FGF, Wnt and TGF-β) have not been identified in the FetMSCs secretome. |
format | Online Article Text |
id | pubmed-7716221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77162212020-12-05 Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome Lobov, Arseniy A. Yudintceva, Natalia M. Mittenberg, Alexey G. Shabelnikov, Sergey V. Mikhailova, Natalia A. Malashicheva, Anna B. Khotin, Mikhail G. Molecules Article Secretome of multipotent mesenchymal stromal cells (MSCs) is actively used in biomedical applications such as alveolar bone regeneration, treatment of cardiovascular disease, and neurodegenerative disorders. Nevertheless, hMSCs have low proliferative potential and production of the industrial quantity of their secretome might be challenging. Human fetal multipotent mesenchymal stromal cells (FetMSCs) isolated from early human embryo bone marrow are easy to expand and might be a potential source for pharmaceutical substances production based on their secretome. However, the secretome of FetMSCs was not previously analyzed. Here, we describe the secretome of FetMSCs using LC-MALDI shotgun proteomics. We identified 236 proteins. Functional annotation of the identified proteins revealed their involvement in angiogenesis, ossification, regulation of apoptosis, and immune response processes, which made it promising for biomedical applications. The proteins identified in the FetMSCs secretome are involved in the same biological processes as proteins from previously described adult hMSCs secretomes. Nevertheless, many of the common hMSCs secretome components (such as VEGF, FGF, Wnt and TGF-β) have not been identified in the FetMSCs secretome. MDPI 2020-11-12 /pmc/articles/PMC7716221/ /pubmed/33198321 http://dx.doi.org/10.3390/molecules25225283 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lobov, Arseniy A. Yudintceva, Natalia M. Mittenberg, Alexey G. Shabelnikov, Sergey V. Mikhailova, Natalia A. Malashicheva, Anna B. Khotin, Mikhail G. Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title | Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title_full | Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title_fullStr | Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title_full_unstemmed | Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title_short | Proteomic Profiling of the Human Fetal Multipotent Mesenchymal Stromal Cells Secretome |
title_sort | proteomic profiling of the human fetal multipotent mesenchymal stromal cells secretome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716221/ https://www.ncbi.nlm.nih.gov/pubmed/33198321 http://dx.doi.org/10.3390/molecules25225283 |
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