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Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources

BACKGROUND: Mesenchymal stem cells (MSCs) are undifferentiated cells that can give rise to a mesoderm lineage. Adipose-derived MSCs are an easy and accessible source for MSCs isolation, although each source of MSC has its own advantages and disadvantages. Our study identifies a promising source for...

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Autores principales: Rashid, Usman, Yousaf, Arfan, Yaqoob, Muhammad, Saba, Evelyn, Moaeen-ud-Din, Muhammad, Waseem, Shahid, Becker, Sandra K., Sponder, Gerhard, Aschenbach, Jörg R., Sandhu, Mansur Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684202/
https://www.ncbi.nlm.nih.gov/pubmed/34922529
http://dx.doi.org/10.1186/s12917-021-03100-8
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author Rashid, Usman
Yousaf, Arfan
Yaqoob, Muhammad
Saba, Evelyn
Moaeen-ud-Din, Muhammad
Waseem, Shahid
Becker, Sandra K.
Sponder, Gerhard
Aschenbach, Jörg R.
Sandhu, Mansur Abdullah
author_facet Rashid, Usman
Yousaf, Arfan
Yaqoob, Muhammad
Saba, Evelyn
Moaeen-ud-Din, Muhammad
Waseem, Shahid
Becker, Sandra K.
Sponder, Gerhard
Aschenbach, Jörg R.
Sandhu, Mansur Abdullah
author_sort Rashid, Usman
collection PubMed
description BACKGROUND: Mesenchymal stem cells (MSCs) are undifferentiated cells that can give rise to a mesoderm lineage. Adipose-derived MSCs are an easy and accessible source for MSCs isolation, although each source of MSC has its own advantages and disadvantages. Our study identifies a promising source for the isolation and differentiation of canines MSCs. For this purpose, adipose tissue from inguinal subcutaneous (SC), perirenal (PR), omental (OM), and infrapatellar fat pad (IPFP) was isolated and processed for MSCs isolation. In the third passage, MSCs proliferation/metabolism, surface markers expression, in vitro differentiation potential and quantitative reverse transcription PCR (CD73, CD90, CD105, PPARγ, FabP4, FAS, SP7, Osteopontin, and Osteocalcin) were evaluated. RESULTS: Our results showed that MSCs derived from IPFP have a higher proliferation rate, while OM-derived MSCs have higher cell metabolism. In addition, MSCs from all adipose tissue sources showed positive expression of CD73 (NT5E), CD90 (THY1), CD105 (ENDOGLIN), and very low expression of CD45. The isolated canine MSCs were successfully differentiated into adipogenic and osteogenic lineages. The oil-red-O quantification and adipogenic gene expression (FAS, FabP4, and PPARγ) were higher in OM-derived cells, followed by IPFP-MSCs. Similarly, in osteogenic differentiation, alkaline phosphatase activity and osteogenic gene (SP7 and Osteocalcin) expression were higher in OM-derived MSCs, while osteopontin expression was higher in PR-derived MSCs. CONCLUSION: In summary, among all four adipose tissue sources, OM-derived MSCs have better differentiation potential toward adipo- and osteogenic lineages, followed by IPFP-MSCs. Interestingly, among all adipose tissue sources, MSCs derived from IPFP have the maximum proliferation potential. The characterization and differentiation potential of canine MSCs isolated from four different adipose tissue sources are useful to assess their potential for application in regenerative medicine.
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spelling pubmed-86842022021-12-20 Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources Rashid, Usman Yousaf, Arfan Yaqoob, Muhammad Saba, Evelyn Moaeen-ud-Din, Muhammad Waseem, Shahid Becker, Sandra K. Sponder, Gerhard Aschenbach, Jörg R. Sandhu, Mansur Abdullah BMC Vet Res Research BACKGROUND: Mesenchymal stem cells (MSCs) are undifferentiated cells that can give rise to a mesoderm lineage. Adipose-derived MSCs are an easy and accessible source for MSCs isolation, although each source of MSC has its own advantages and disadvantages. Our study identifies a promising source for the isolation and differentiation of canines MSCs. For this purpose, adipose tissue from inguinal subcutaneous (SC), perirenal (PR), omental (OM), and infrapatellar fat pad (IPFP) was isolated and processed for MSCs isolation. In the third passage, MSCs proliferation/metabolism, surface markers expression, in vitro differentiation potential and quantitative reverse transcription PCR (CD73, CD90, CD105, PPARγ, FabP4, FAS, SP7, Osteopontin, and Osteocalcin) were evaluated. RESULTS: Our results showed that MSCs derived from IPFP have a higher proliferation rate, while OM-derived MSCs have higher cell metabolism. In addition, MSCs from all adipose tissue sources showed positive expression of CD73 (NT5E), CD90 (THY1), CD105 (ENDOGLIN), and very low expression of CD45. The isolated canine MSCs were successfully differentiated into adipogenic and osteogenic lineages. The oil-red-O quantification and adipogenic gene expression (FAS, FabP4, and PPARγ) were higher in OM-derived cells, followed by IPFP-MSCs. Similarly, in osteogenic differentiation, alkaline phosphatase activity and osteogenic gene (SP7 and Osteocalcin) expression were higher in OM-derived MSCs, while osteopontin expression was higher in PR-derived MSCs. CONCLUSION: In summary, among all four adipose tissue sources, OM-derived MSCs have better differentiation potential toward adipo- and osteogenic lineages, followed by IPFP-MSCs. Interestingly, among all adipose tissue sources, MSCs derived from IPFP have the maximum proliferation potential. The characterization and differentiation potential of canine MSCs isolated from four different adipose tissue sources are useful to assess their potential for application in regenerative medicine. BioMed Central 2021-12-18 /pmc/articles/PMC8684202/ /pubmed/34922529 http://dx.doi.org/10.1186/s12917-021-03100-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Rashid, Usman
Yousaf, Arfan
Yaqoob, Muhammad
Saba, Evelyn
Moaeen-ud-Din, Muhammad
Waseem, Shahid
Becker, Sandra K.
Sponder, Gerhard
Aschenbach, Jörg R.
Sandhu, Mansur Abdullah
Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title_full Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title_fullStr Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title_full_unstemmed Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title_short Characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
title_sort characterization and differentiation potential of mesenchymal stem cells isolated from multiple canine adipose tissue sources
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684202/
https://www.ncbi.nlm.nih.gov/pubmed/34922529
http://dx.doi.org/10.1186/s12917-021-03100-8
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