A Comparative Study Using Fluorescent Confocal Microscopy and Flow Cytometry to Evaluate Chondrocyte Viability in Human Osteochondral Allografts.
Patricia López-ChicónTatiana Riba-TietzOscar FariñasPablo-Eduardo GelberRicardo-Pedro Casaroli-MaranoAnna VilarrodonaPublished in: Bioengineering (Basel, Switzerland) (2022)
The preservation conditions of fresh osteochondral allografts for clinical applications are critical due their objective: to transplant mature hyaline cartilage containing viable chondrocytes, maintaining their metabolic activity and also preserving the structural and functional characteristics of the extracellular matrix. The aim of the present study was to compare fluorescence confocal microscopy and flow cytometry techniques to evaluate the viability of the chondrocytes present in the osteochondral tissue, in order to determine their effectiveness and thus ensure reproducibility and robustness of the analysis. To this end, osteochondral allografts from human cadaveric donors were preserved at 4 °C for 3 weeks in a preservation medium supplemented with antibiotic and antifungal agents. Cell viability of chondrocytes was determined by monitoring the cartilage for 3 weeks of preservation by confocal fluorescence microscopy and flow cytometry, obtaining cell viabilities of 83.7 ± 2.6% and 55.8 ± 7.8% for week three, respectively. The confocal fluorescence microscopy approach is more advantageous and accurate, as it correlates better with actual cell viability values for monitoring osteochondral graft preservation, detecting only the cells that died a natural death associated with the preservation method.
Keyphrases
- flow cytometry
- extracellular matrix
- single molecule
- platelet rich plasma
- endothelial cells
- optical coherence tomography
- high resolution
- randomized controlled trial
- induced apoptosis
- energy transfer
- systematic review
- high throughput
- clinical trial
- quantum dots
- single cell
- stem cells
- oxidative stress
- gestational age
- cell proliferation
- mass spectrometry
- cell cycle arrest
- study protocol