Study of Mesenchymal Stem Cells Cultured on a Poly(Lactic-co-Glycolic Acid) Scaffold Containing Simvastatin for Bone Healing
Background Tissue engineering is a promising alternative for the development of bone substitutes; for this purpose, three things are necessary: stem cells, a scaffold to allow tissue growth and factors that induce tissue regeneration. Methods To congregate such efforts, we used the bioresorbable and...
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Veröffentlicht in: | Journal of applied biomaterials & functional materials 2017-04, Vol.15 (2), p.133-141 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Tissue engineering is a promising alternative for the development of bone
substitutes; for this purpose, three things are necessary: stem cells, a
scaffold to allow tissue growth and factors that induce tissue
regeneration.
Methods
To congregate such efforts, we used the bioresorbable and biocompatible
polymer poly(lactic-co-glycolic acid) (PLGA) as scaffold. For the
osteoinductive factor, we used simvastatin (SIM), a drug with a pleiotropic
effect on bone growth. Mesenchymal stem cells (MSCs) were cultured in PLGA
containing SIM, and the bone substitute of PLGA/SIM/MSC was grafted into
critical defects of rat calvaria.
Results
The in vitro results showed that SIM directly interfered with the
proliferation of MSC promoting cell death, while in the pure PLGA scaffold
the MSC grew continuously. Scaffolds were implanted in the calvaria of rats
and separated into groups: control (empty defect), PLGA pure, PLGA/SIM,
PLGA/MSC and PLGA/SIM/MSC. The increase in bone growth was higher in the
PLGA/SIM group.
Conclusions
We observed no improvement in the growth of bone tissue after implantation of
the PLGA/SIM/MSC scaffold. As compared with in vitro results, our main
hypothesis is that the microarchitecture of PLGA associated with low SIM
release would have created an in vivo microenvironment of concentrated SIM
that might have induced MSC death. However, our findings indicate that once
implanted, both PLGA/SIM and PLGA/MSC contributed to bone formation. We
suggest that strategies to maintain the viability of MSCs after cultivation
in PLGA/SIM will contribute to improvement of bone regeneration. |
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ISSN: | 2280-8000 2280-8000 |
DOI: | 10.5301/jabfm.5000338 |