Effect of biomolecules derived from human platelet-rich plasma on the ex vivo expansion of human adipose-derived mesenchymal stem cells for clinical applications. (January 2022)
- Record Type:
- Journal Article
- Title:
- Effect of biomolecules derived from human platelet-rich plasma on the ex vivo expansion of human adipose-derived mesenchymal stem cells for clinical applications. (January 2022)
- Main Title:
- Effect of biomolecules derived from human platelet-rich plasma on the ex vivo expansion of human adipose-derived mesenchymal stem cells for clinical applications
- Authors:
- Becerra-Bayona, Silvia M.
Solarte, Víctor Alfonso
Alviar Rueda, Juan David
Sossa, Claudia L.
Arango-Rodríguez, Martha L. - Abstract:
- Abstract: Mesenchymal stem cells are a tool in cell therapies but demand a large cell number per treatment, for that, suitable culture media is required which contains fetal bovine serum (FBS). However, for cell-based therapy applications, the use of FBS is problematic. Several alternatives to FBS have been explored, including human derivatives from platelet-rich plasma (hD-PRP). Although various studies have evaluated the impact of hD-PRP on MSC proliferation and differentiation, few of them have assessed their influence on processes, such as metabolism and gene expression. Here, we cultured human adipose-derived MSCs (hAD-MSCs) in media supplemented with either 10% hD-PRP (hD-PRP-SM) or 10% FBS (FBS-SM) in order to characterize them and evaluate the effect of hD-PRP on cell metabolism, gene expression of associated regenerative factors, as well as chromosome stability during cell expansion. We found that hAD-MSCs cultured in hD-PRP-SM have a greater cell elongation but express similar surface markers; in addition, hD-PRP-SM promoted a significant osteogenic differentiation in the absence of differentiation medium and increased the growth rate, maintaining chromosomal stability. In terms of cell metabolic profile, hAD-MSC behavior did not reveal any differences between both culture conditions. Conversely, significant differences in collagen I and angiopoietin 2 expression were observed between both conditions. The present results suggest that hD-PRP may influence hAD-MSCAbstract: Mesenchymal stem cells are a tool in cell therapies but demand a large cell number per treatment, for that, suitable culture media is required which contains fetal bovine serum (FBS). However, for cell-based therapy applications, the use of FBS is problematic. Several alternatives to FBS have been explored, including human derivatives from platelet-rich plasma (hD-PRP). Although various studies have evaluated the impact of hD-PRP on MSC proliferation and differentiation, few of them have assessed their influence on processes, such as metabolism and gene expression. Here, we cultured human adipose-derived MSCs (hAD-MSCs) in media supplemented with either 10% hD-PRP (hD-PRP-SM) or 10% FBS (FBS-SM) in order to characterize them and evaluate the effect of hD-PRP on cell metabolism, gene expression of associated regenerative factors, as well as chromosome stability during cell expansion. We found that hAD-MSCs cultured in hD-PRP-SM have a greater cell elongation but express similar surface markers; in addition, hD-PRP-SM promoted a significant osteogenic differentiation in the absence of differentiation medium and increased the growth rate, maintaining chromosomal stability. In terms of cell metabolic profile, hAD-MSC behavior did not reveal any differences between both culture conditions. Conversely, significant differences in collagen I and angiopoietin 2 expression were observed between both conditions. The present results suggest that hD-PRP may influence hAD-MSC behavior. Highlights: Human derivatives from platelet-rich plasma is an alternatives to fetal bovine serum. Human derivatives from platelet-rich plasma promoted perse a significant osteogenic differentiation. Human derivatives from platelet-rich plasma increase the growth rate. Human derivatives from platelet-rich plasma may influence mesenchymal stem cells behavior. … (more)
- Is Part Of:
- Biologicals. Volume 75(2022)
- Journal:
- Biologicals
- Issue:
- Volume 75(2022)
- Issue Display:
- Volume 75, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 75
- Issue:
- 2022
- Issue Sort Value:
- 2022-0075-2022-0000
- Page Start:
- 37
- Page End:
- 48
- Publication Date:
- 2022-01
- Subjects:
- Fetal bovine serum FBS -- Human derivatives from platelet-rich plasma hD-PRP -- human adipose-derived MSCs hAD-MSCs -- media supplemented with hD-PRP hD-PRP-SM -- media supplemented with FBS FBS-SM -- Mesenchymal stem cells MSCs -- Bone marrow BM -- Adipose tissue AD -- umbilical cord blood UCB -- Human AD-MSC hAD-MSC -- Citrate phosphate dextose adenine 1 CPDA-1 -- Good manufacturing practice GMP -- Stromal vascular cells SVF -- Room temperature RT -- Phosphate buffer solution PBS -- Cumulative population doubling level CPDL -- Population doubling PD -- Standar deviation SD -- Xenogeneic serum free medium XFM -- Society for Cell Tharapy ISCT -- Peroxisome Proliferator-Activated Receptor PPAR -- Adipocyte Protein 2 aP2 -- Mitogen activated protein kinase MAPK -- Extracellular signal-regulated kinase ERK -- c-Jun N-terminal kinase JNK
Human adipose-derived mesenchymal stem cell -- Fetal bovine serum -- Human derivatives from platelet-rich plasma -- Clinical applications
Biological products -- Standards -- Periodicals
Biological Products -- Periodicals
Biological Products -- standards -- Periodicals
Produits biologiques -- Normes -- Périodiques
Biological products -- Standards
Periodicals
615.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10451056 ↗
http://www.elsevier.com/journals ↗
http://firstsearch.oclc.org/journal=1045-1056;screen=info;ECOIP ↗ - DOI:
- 10.1016/j.biologicals.2021.11.001 ↗
- Languages:
- English
- ISSNs:
- 1045-1056
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2081.670000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20675.xml