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Cre mRNA Is Not Transferred by EVs from Endothelial and Adipose-Derived Stromal/Stem Cells during Vascular Network Formation.
Schneider, Jaana; Pultar, Marianne; Oesterreicher, Johannes; Bobbili, Madhusudhan Reddy; Mühleder, Severin; Priglinger, Eleni; Redl, Heinz; Spittler, Andreas; Grillari, Johannes; Holnthoner, Wolfgang.
Afiliación
  • Schneider J; AUVA Research Centre, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, 1200 Vienna, Austria.
  • Pultar M; Austrian Cluster for Tissue Regeneration, 1200 Vienna, Austria.
  • Oesterreicher J; AUVA Research Centre, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, 1200 Vienna, Austria.
  • Bobbili MR; Austrian Cluster for Tissue Regeneration, 1200 Vienna, Austria.
  • Mühleder S; AUVA Research Centre, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, 1200 Vienna, Austria.
  • Priglinger E; Austrian Cluster for Tissue Regeneration, 1200 Vienna, Austria.
  • Redl H; AUVA Research Centre, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, 1200 Vienna, Austria.
  • Spittler A; Austrian Cluster for Tissue Regeneration, 1200 Vienna, Austria.
  • Grillari J; Centro Nacional de Investigaciones Cardiovasculares (CNIC), Molecular Genetics of Angiogenesis Group, 28029 Madrid, Spain.
  • Holnthoner W; AUVA Research Centre, Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, 1200 Vienna, Austria.
Int J Mol Sci ; 22(8)2021 Apr 14.
Article en En | MEDLINE | ID: mdl-33919955
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Asunto principal: Integrasas / MicroARNs / Células Madre Mesenquimatosas / Vesículas Extracelulares Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Asunto principal: Integrasas / MicroARNs / Células Madre Mesenquimatosas / Vesículas Extracelulares Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Austria