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Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells
Extracellular vesicles (EV) awakened interest in the research on mesenchymal stromal cells by exploring their paracrine effects. However, many isolation protocols use bovine serum albumin (BSA) during the preparation of the EV. Therefore, we produced ‘sham’ BSA-EV and tested them in comparison to EV...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Journal of Stem Cells and Regenerative Medicine
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728215/ https://www.ncbi.nlm.nih.gov/pubmed/27330254 |
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author | Stolk, Meaghan Seifert, Martina |
author_facet | Stolk, Meaghan Seifert, Martina |
author_sort | Stolk, Meaghan |
collection | PubMed |
description | Extracellular vesicles (EV) awakened interest in the research on mesenchymal stromal cells by exploring their paracrine effects. However, many isolation protocols use bovine serum albumin (BSA) during the preparation of the EV. Therefore, we produced ‘sham’ BSA-EV and tested them in comparison to EV derived from mesenchymal stromal cells (MSC-EV). We found that BSA-EV did not express MSC-specific surface markers like CD29 and CD90. However, they were capable of reducing serum-starvation induced apoptosis in vitro in a kidney epithelial cell line to a similar extent as MSC-EV as measured by Annexin V/7-Aminoactinomycin D labeling and flow cytometry. |
format | Online Article Text |
id | pubmed-4728215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Journal of Stem Cells and Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-47282152016-06-21 Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells Stolk, Meaghan Seifert, Martina J Stem Cells Regen Med Brief Communication Extracellular vesicles (EV) awakened interest in the research on mesenchymal stromal cells by exploring their paracrine effects. However, many isolation protocols use bovine serum albumin (BSA) during the preparation of the EV. Therefore, we produced ‘sham’ BSA-EV and tested them in comparison to EV derived from mesenchymal stromal cells (MSC-EV). We found that BSA-EV did not express MSC-specific surface markers like CD29 and CD90. However, they were capable of reducing serum-starvation induced apoptosis in vitro in a kidney epithelial cell line to a similar extent as MSC-EV as measured by Annexin V/7-Aminoactinomycin D labeling and flow cytometry. Journal of Stem Cells and Regenerative Medicine 2015-12-31 /pmc/articles/PMC4728215/ /pubmed/27330254 Text en Copyright © Journal of Stem Cells and Regenerative Medicine |
spellingShingle | Brief Communication Stolk, Meaghan Seifert, Martina Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title | Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title_full | Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title_fullStr | Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title_full_unstemmed | Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title_short | Protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
title_sort | protein contaminations impact quantification and functional analysis of extracellular vesicle preparations from mesenchymal stromal cells |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728215/ https://www.ncbi.nlm.nih.gov/pubmed/27330254 |
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