Characterization and Cytotoxicity Evaluation of a Marine Sponge Biosilica

Mar Biotechnol (NY). 2019 Feb;21(1):65-75. doi: 10.1007/s10126-018-9858-9. Epub 2018 Nov 16.

Abstract

Bone fractures characterize an important event in the medical healthcare, being related to traumas, aging, and diseases. In critical conditions, such as extensive bone loss and osteoporosis, the tissue restoration may be compromised and culminate in a non-union consolidation. In this context, the osteogenic properties of biomaterials with a natural origin have gained prominence. Particularly, marine sponges are promising organisms that can be exploited as biomaterials for bone grafts. Thus, the objectives of this study were to study the physicochemical and morphological properties of biosilica (BS) from sponges by using scanning electron microscopy, Fourier-transform infrared, X-ray diffraction (SEM, FTIR and XRD respectively), mineralization, and pH. In addition, tests on an osteoblast precursor cell line (MC3T3-E1) were performed to investigate its cytotoxicity and proliferation in presence of BS. Bioglass (BG) was used as gold standard material for comparison purposes. Sponge BS was obtained, and this fact was proven by SEM, FTIR, and XRD analysis. Calcium assay showed a progressive release of this ion from day 7 and a more balanced pH for BS was maintained compared to BG. Cytotoxicity assay indicated that BS had a positive influence on MC3T3-E1 cells viability and qRT-PCR showed that this material stimulated Runx2 and BMP4 gene expressions. Taken together, the results indicate a potential use of sponge biosilica for tissue engineering applications.

Keywords: Bioglass; Biosilica; Bone repair; Cytotoxicity; Porifera.

MeSH terms

  • Animals
  • Biocompatible Materials / isolation & purification
  • Biocompatible Materials / pharmacology*
  • Biomarkers / metabolism
  • Bone Morphogenetic Protein 4 / genetics
  • Bone Morphogenetic Protein 4 / metabolism
  • Bone Substitutes / isolation & purification
  • Bone Substitutes / pharmacology*
  • Bone and Bones / cytology
  • Bone and Bones / drug effects
  • Bone and Bones / metabolism
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Core Binding Factor Alpha 1 Subunit / genetics
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Fractures, Bone / therapy
  • Gene Expression
  • Humans
  • Mice
  • Osteoblasts / cytology
  • Osteoblasts / drug effects*
  • Osteoblasts / metabolism
  • Porifera / chemistry*
  • Silicon Dioxide / isolation & purification
  • Silicon Dioxide / pharmacology*
  • Tissue Engineering / methods

Substances

  • Biocompatible Materials
  • Biomarkers
  • Bmp4 protein, mouse
  • Bone Morphogenetic Protein 4
  • Bone Substitutes
  • Core Binding Factor Alpha 1 Subunit
  • Runx2 protein, mouse
  • Silicon Dioxide