4.3 Article

Mitochondrial Transport from Mesenchymal Stromal Cells to Chondrocytes Increases DNA Content and Proteoglycan Deposition In Vitro in 3D Cultures

Journal

CARTILAGE
Volume 13, Issue 4, Pages 133-147

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/19476035221126346

Keywords

cartilage repair; repair; mesenchymal stem cells; cells; articular cartilage; tissue; mitochondria; cell communication

Categories

Funding

  1. ZonMw (the Netherlands Organization for Health Research and Development) TAS [116004103]
  2. Strategic theme Regenerative Medicine & Stem cells of the University Medical Center Utrecht
  3. RegMed XB

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This study found that there is transport of mitochondria between mesenchymal stromal cells (MSCs) and chondrocytes, which may contribute to the mechanism of action of MSCs on chondrocytes. However, no transferred mitochondria could be traced back in vivo.
Objective Allogeneic mesenchymal stromal cells (MSCs) are used in the 1-stage treatment of articular cartilage defects. The aim of this study is to investigate whether transport of mitochondria exists between chondrocytes and MSCs and to investigate whether the transfer of mitochondria to chondrocytes contributes to the mechanism of action of MSCs. Design Chondrocytes and MSCs were stained with MitoTracker, and CellTrace was used to distinguish between cell types. The uptake of fluorescent mitochondria was measured in cocultures using flow cytometry. Transport was visualized using fluorescence microscopy. Microvesicles were isolated and the presence of mitochondria was assessed. Mitochondria were isolated from MSCs and transferred to chondrocytes using MitoCeption. Pellets of chondrocytes, chondrocytes with transferred MSC mitochondria, and cocultures were cultured for 28 days. DNA content and proteoglycan content were measured. Mitochondrial DNA of cultured pellets and of repair cartilage tissue was quantified. Results Mitochondrial transfer occurred bidirectionally within the first 4 hours until 16 hours of coculture. Transport took place via tunneling nanotubes, direct cell-cell contact, and extracellular vesicles. After 28 days of pellet culture, DNA content and proteoglycan deposition were higher in chondrocyte pellets to which MSC mitochondria were transferred than the control groups. No donor mitochondrial DNA was traceable in the biopsies, whereas an increase in MSC mitochondrial DNA was seen in the pellets. Conclusions These results suggest that mitochondrial transport plays a role in the chondroinductive effect of MSCs on chondrocytes in vitro. However, in vivo no transferred mitochondria could be traced back after 1 year.

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