Comparative assessment of human chondroprogenitor viability and molecular phenotype in various parenteral transport media
- Jeya Lisha John 1, Gurbind Singh 2, Ganesh Parasuraman 2, Abel Livingston 3, Grace Rebekah 4, Alfred Job Daniel 3, Solomon Sathishkumar 1, Elizabeth Vinod 5,6
- 1Department of Physiology, Christian Medical College, Vellore, Tamil Nadu, 632002, India.
- 2Centre of Stem Cell Research, (a unit of BRIC-inStem, Bengaluru), Christian Medical College, Vellore, Tamil Nadu, India.
- 3Department of Orthopaedics, Christian Medical College, Vellore, Tamil Nadu, India.
- 4Department of Biostatistics, Christian Medical College, Vellore, Tamil Nadu, India.
- 5Department of Physiology, Christian Medical College, Vellore, Tamil Nadu, 632002, India. elsyclarence@cmcvellore.ac.in.
- 6Centre of Stem Cell Research, (a unit of BRIC-inStem, Bengaluru), Christian Medical College, Vellore, Tamil Nadu, India. elsyclarence@cmcvellore.ac.in.
- 0Department of Physiology, Christian Medical College, Vellore, Tamil Nadu, 632002, India.
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View abstract on PubMed
Summary
This summary is machine-generated.Optimal parenteral solutions like normal saline, Plasma-lyte A, and 5% dextrose preserve chondroprogenitor cells for up to 12 hours. 5% dextrose shows potential for cartilage repair due to low hypertrophic markers.
Area Of Science
- Regenerative Medicine
- Biomaterials Science
- Cell Biology
Background
- Articular cartilage-derived chondroprogenitors are promising for cartilage repair.
- Optimizing cell transport solutions is critical for clinical application.
- Maintaining cell viability and function during storage is essential.
Purpose Of The Study
- To evaluate the impact of different parenteral solutions on chondroprogenitor cell viability, phenotype, and differentiation.
- To determine optimal storage conditions for chondroprogenitors for up to 12 hours at 4°C.
- To identify the best cell-delivery vehicle for cartilage regeneration.
Main Methods
- Human fibronectin adhesion assay-derived chondroprogenitors (FAA-CPs) were suspended in normal saline, Plasma-lyte A, 5% dextrose, hyaluronic acid, or platelet-rich plasma.
- Cells were stored at 4°C for 0, 6, and 12 hours.
- Viability was assessed using Vi-CELL BLU and calcein AM-propidium iodide staining.
- Chondrogenic marker expression and differentiation potential were evaluated.
Main Results
- Viability was maintained in normal saline, Plasma-lyte A, 5% dextrose, and hyaluronic acid, but decreased in platelet-rich plasma.
- All solutions retained multilineage differentiation potential.
- Enhanced chondrogenesis was observed in normal saline, Plasma-lyte A, and 5% dextrose.
- 5% dextrose demonstrated minimal collagen X accumulation, indicating low hypertrophic potential.
Conclusions
- Normal saline, Plasma-lyte A, and 5% dextrose are optimal parenteral solutions for chondroprogenitor suspensions up to 12 hours.
- 5% dextrose is a promising cell-delivery vehicle for cartilage disease treatment due to its low hypertrophic potential.
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