Proliferation Assessment of Primary Human Mesenchymal Stem Cells on Collagen Membranes for Guided Bone Regeneration.
| Autor: | Qin Liu, Humpe, Andreas, Kletsas, Dimitris, Warnke, Frauke, Becker, Stephan T., Douglas, Timothy, Sivananthan, Sureshan, Warnke, Patrick H. |
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| Předmět: |
GUIDED tissue regeneration
STEM cells BONE marrow physiology GLASS BIOMEDICAL materials BONE regeneration CELL culture CHEMICAL reagents COLLAGEN COMPARATIVE studies CONFIDENCE intervals FLOW cytometry IMIDAZOLES LIQUIDS PROPERTIES of matter ARTIFICIAL membranes MICROSCOPICAL technique OXIDOREDUCTASES PROBABILITY theory RESEARCH funding SCANNING electron microscopy STAINS & staining (Microscopy) TIME PHYSIOLOGY |
| Zdroj: | International Journal of Oral & Maxillofacial Implants; 2011, Vol. 26 Issue 5, p1004-1010, 7p, 1 Color Photograph, 1 Black and White Photograph, 4 Graphs |
| Abstrakt: | Purpose: Human mesenchymal stem cells (hMSCs) hold the potential for bone regeneration because of their self-renewing and multipotent character. The goal of this study was to evaluate the influence of collagen membranes on the proliferation of hMSCs derived from bone marrow. A special focus was set on short-term eluates derived from collagen membranes, as volatile toxic materials washed out from these membranes may influence cell behavior during the short time course of oral surgery. Materials and Methods: The proliferation of hMSCs seeded directly on a collagen membrane (BioGide) was evaluated quantitatively using the cell proliferation reagent WST-1 (4-3-[4-iodophenyl]-2-[4-nitrophenyl]-2H-[5-tetrazolio]-1, 3-benzoldisulfonate) and qualitatively by scanning electron microscopy. Two standard biocompatibility tests, namely the lactate dehydrogenase and MTT (3-[4, 5-dimethyl-2-thiazolyl]-2, 5-diphenyl-2H-tetrazoliumbromide) tests, were performed using hMSCs cultivated in eluates from membranes incubated for 10 minutes, 1 hour, or 24 hours in serum-free cell culture medium. The data were analyzed statistically. Results: Scanning electron microscopy showed large numbers of hMSCs with well-spread morphology on the collagen membranes after 7 days of culture. The WST test revealed significantly better proliferation of hMSCs on collagen membranes after 4 days of culture compared to cells cultured on a cover glass. Cytotoxicity levels were low, peaking in short-term eluates and decreasing with longer incubation times. Conclusion: Porcine collagen membranes showed good biocompatibility in vitro for hMSCs. If maximum cell proliferation rates are required, a prewash of membranes prior to application may be useful. [ABSTRACT FROM AUTHOR] |
| Databáze: | Complementary Index |
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