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Cre mRNA Is Not Transferred by EVs from Endothelial and Adipose-Derived Stromal/Stem Cells during Vascular Network Formation

  • Coculture systems employing adipose tissue-derived mesenchymal stromal/stem cells (ASC) and endothelial cells (EC) represent a widely used technique to model vascularization. Within this system, cell-cell communication is crucial for the achievement of functional vascular network formation. Extracellular vesicles (EVs) have recently emerged as key players in cell communication by transferring bioactive molecules between cells. In this study we aimed to address the role of EVs in ASC/EC cocultures by discriminating between cells, which have received functional EV cargo from cells that have not. Therefore, we employed the Cre-loxP system, which is based on donor cells expressing the Cre recombinase, whose mRNA was previously shown to be packaged into EVs and reporter cells containing a construct of floxed dsRed upstream of the eGFP coding sequence. The evaluation of Cre induced color switch in the reporter system via EVs indicated that there is no EV-mediated RNA transmission either between EC themselves or EC and ASC. However, since Cre mRNA was not found present in EVs, it remains unclear if Cre mRNA is generally not packaged into EVs or if EVs are not taken up by the utilized cell types. Our data indicate that this technique may not be applicable to evaluate EV-mediated cell-to-cell communication in an in vitro setting using EC and ASC. Further investigations will require a functional system showing efficient and specific loading of Cre mRNA or protein into EVs.

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Author:Jaana Schneider, Marianne Pultar, Johannes Oesterreicher, Madhusudhan Reddy Bobbili, Severin Mühleder, Eleni Priglinger, Heinz Redl, Andreas Spittler, Johannes Grillari, Wolfgang HolnthonerORCiD
Parent Title (English):Int J Mol Sci.
Document Type:Article
Language:English
Completed Date:2021/04/14
Responsibility for metadata:Fachhochschule Technikum Wien
Release Date:2023/01/16
GND Keyword:EVs; Endothelial Cells; Stem Cells; Tissue Engineering; Vascular Network Formation
Volume:2021
Issue:22(8)
First Page:4050
Publish on Website:1
Open Access:1
Reviewed:1
Link to Publication:https://doi.org/10.3390/ijms22084050
Department:Department Life Science Engineering
Research Focus:Tissue Engineering & Molecular Life Science Technologies
Projects:Eigenmittel
Studienjahr:2020/2021
Licence (German):License LogoCreative Commons - CC BY - Namensnennung 4.0 International