The effects of oyster shell/alpha-calcium sulfate hemihydrate/platelet-rich plasma/bone mesenchymal stem cells bioengineering scaffold on rat critical-sized calvarial defects
Creators
- 1. Wenzhou Medical University (China)
- 2. The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University. Department of Orthopaedics Surgery (China)
Description
Engineering scaffolds combining natural biomineral and artificially synthesized material hold promising potential for bone tissue regeneration. We fabricated a bioengineering scaffold, oyster shell (OS) and alpha-calcium sulfate hemihydrate (α-CSH) as scaffold, platelet-rich plasma (PRP) as provider of growth factors and bone mesenchymal stem cells (BMSCs) as seed cells, and determined it could be applied as a new type of bone graft substitutes by rat calvarial defects repairing experiment in vitro and in vivo. SEM showed that the mean diameter of the pores was about 150 μm with a range of 50–200 μm, and scaffold's porosity was ~27.4% by Archimedes' Principle. In vitro, Scaffold + BMSCs + PRP group presented a higher ALP activity compared with other groups by ELISA (P < 0.05). But the expression of OC was not detectable on day 4 or 8. The MTT assay showed that the relative cell number of BMSCs+PRP group increased significantly (P < 0.05). In vivo, the smallest defect area of skull and highest volume of regenerated new bone were observed in Scaffold + PRP + BMSCs group by X-ray and Micro-CT analysis (P < 0.05). And the similar results also were observed in HE and Masson staining. The immunohistochemistry staining for osteogenic marker proteins ALP and OC showed that the most obvious positive staining was observed in Scaffold + PRP + BMSCs group (P < 0.05). The expression of inflammatory markers IL-6 and TNF-α was the lowest in control group (P < 0.05). In conclusion, a bioengineering scaffold based on OS, created by simply combining α-CSH and PRP and implanting with BMSCs, could be clinically useful and has marked advantages as a targeted, off-the-shelf, cell-loaded treatment option for the bone healing of critical-size calvarial defects.
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Materials Science. Materials in Medicine
- Journal Volume
- 31
- Journal Issue
- 11
- Journal Page Range
- vp.
- ISSN
- 0957-4530
- CODEN
- JSMMEL
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55078210
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BONE CELLS; BONE MINERAL DENSITY; BONE TISSUES; CALCIUM; ENZYME IMMUNOASSAY; GROWTH FACTORS; HEALING; IN VITRO; IN VIVO; INFLAMMATION; POROSITY; RATS; SCANNING ELECTRON MICROSCOPY; SKELETON; STEM CELLS
- Descriptors DEC
- ALKALINE EARTH METALS; ANIMAL CELLS; ANIMAL TISSUES; ANIMALS; BIOASSAY; BIOLOGICAL RECOVERY; BODY; BODY COMPOSITION; CONNECTIVE TISSUE; CONNECTIVE TISSUE CELLS; ELECTRON MICROSCOPY; ELEMENTS; IMMUNOASSAY; MAMMALS; METALS; MICROSCOPY; MITOGENS; ORGANIC COMPOUNDS; ORGANS; PATHOLOGICAL CHANGES; PROTEINS; RODENTS; SOMATIC CELLS; SYMPTOMS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2020 © Springer Science+Business Media, LLC, part of Springer Nature 2020