Heterogeneity of mesenchymal stem cell-derived extracellular vesicles is highly impacted by the tissue/cell source and culture conditions

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

Autorschaft

  • Ciarra Almeria
  • Sebastian Kreß
  • Viktoria Weber
  • Dominik Egger
  • Cornelia Kasper

Externe Organisationen

  • Universität für Bodenkultur Wien (BOKU)
  • Donau-Universitat Krems / Danube University
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer51
Seitenumfang15
FachzeitschriftCell and Bioscience
Jahrgang12
Ausgabenummer1
PublikationsstatusVeröffentlicht - 2 Mai 2022
Extern publiziertJa

Abstract

Extracellular vesicles (EVs) are cell-derived membrane structures exerting major effects in physiological as well as pathological processes by functioning as vehicles for the delivery of biomolecules to their target cells. An increasing number of effects previously attributed to cell-based therapies have been recognized to be actually mediated by EVs derived from the respective cells, suggesting the administration of purified EVs instead of living cells for cell-based therapies. In this review, we focus on the heterogeneity of EVs derived from mesenchymal stem/stromal cells (MSC) and summarize upstream process parameters that crucially affect the resulting therapeutic properties and biological functions. Hereby, we discuss the effects of the cell source, medium composition, 3D culture, bioreactor culture and hypoxia. Furthermore, aspects of the isolation and storage strategies influences EVs are described. Conclusively, optimization of upstream process parameters should focus on controlling MSC-derived EV heterogeneity for specific therapeutic applications. Graphical Abstract: [Figure not available: see fulltext.]

ASJC Scopus Sachgebiete

Zitieren

Heterogeneity of mesenchymal stem cell-derived extracellular vesicles is highly impacted by the tissue/cell source and culture conditions. / Almeria, Ciarra; Kreß, Sebastian; Weber, Viktoria et al.
in: Cell and Bioscience, Jahrgang 12, Nr. 1, 51, 02.05.2022.

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

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abstract = "Extracellular vesicles (EVs) are cell-derived membrane structures exerting major effects in physiological as well as pathological processes by functioning as vehicles for the delivery of biomolecules to their target cells. An increasing number of effects previously attributed to cell-based therapies have been recognized to be actually mediated by EVs derived from the respective cells, suggesting the administration of purified EVs instead of living cells for cell-based therapies. In this review, we focus on the heterogeneity of EVs derived from mesenchymal stem/stromal cells (MSC) and summarize upstream process parameters that crucially affect the resulting therapeutic properties and biological functions. Hereby, we discuss the effects of the cell source, medium composition, 3D culture, bioreactor culture and hypoxia. Furthermore, aspects of the isolation and storage strategies influences EVs are described. Conclusively, optimization of upstream process parameters should focus on controlling MSC-derived EV heterogeneity for specific therapeutic applications. Graphical Abstract: [Figure not available: see fulltext.]",
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TY - JOUR

T1 - Heterogeneity of mesenchymal stem cell-derived extracellular vesicles is highly impacted by the tissue/cell source and culture conditions

AU - Almeria, Ciarra

AU - Kreß, Sebastian

AU - Weber, Viktoria

AU - Egger, Dominik

AU - Kasper, Cornelia

N1 - Funding Information: No applicable.

PY - 2022/5/2

Y1 - 2022/5/2

N2 - Extracellular vesicles (EVs) are cell-derived membrane structures exerting major effects in physiological as well as pathological processes by functioning as vehicles for the delivery of biomolecules to their target cells. An increasing number of effects previously attributed to cell-based therapies have been recognized to be actually mediated by EVs derived from the respective cells, suggesting the administration of purified EVs instead of living cells for cell-based therapies. In this review, we focus on the heterogeneity of EVs derived from mesenchymal stem/stromal cells (MSC) and summarize upstream process parameters that crucially affect the resulting therapeutic properties and biological functions. Hereby, we discuss the effects of the cell source, medium composition, 3D culture, bioreactor culture and hypoxia. Furthermore, aspects of the isolation and storage strategies influences EVs are described. Conclusively, optimization of upstream process parameters should focus on controlling MSC-derived EV heterogeneity for specific therapeutic applications. Graphical Abstract: [Figure not available: see fulltext.]

AB - Extracellular vesicles (EVs) are cell-derived membrane structures exerting major effects in physiological as well as pathological processes by functioning as vehicles for the delivery of biomolecules to their target cells. An increasing number of effects previously attributed to cell-based therapies have been recognized to be actually mediated by EVs derived from the respective cells, suggesting the administration of purified EVs instead of living cells for cell-based therapies. In this review, we focus on the heterogeneity of EVs derived from mesenchymal stem/stromal cells (MSC) and summarize upstream process parameters that crucially affect the resulting therapeutic properties and biological functions. Hereby, we discuss the effects of the cell source, medium composition, 3D culture, bioreactor culture and hypoxia. Furthermore, aspects of the isolation and storage strategies influences EVs are described. Conclusively, optimization of upstream process parameters should focus on controlling MSC-derived EV heterogeneity for specific therapeutic applications. Graphical Abstract: [Figure not available: see fulltext.]

KW - Cell Culture Conditions

KW - Extracellular vesicles

KW - Mesenchymal Stem Cells

KW - Regenerative Medicine

KW - Scalability

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U2 - 10.1186/s13578-022-00786-7

DO - 10.1186/s13578-022-00786-7

M3 - Review article

AN - SCOPUS:85129294378

VL - 12

JO - Cell and Bioscience

JF - Cell and Bioscience

SN - 2045-3701

IS - 1

M1 - 51

ER -

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