| Autor: |
Nogueira LFB; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil.; Department of Experimental Medicine, University of Rome Tor Vergata, 00133 Rome, Italy., Cruz MAE; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil., de Melo MT; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil., Maniglia BC; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil., Caroleo F; Department of Chemical Science and Technology, University of Rome Tor Vergata, 00133 Rome, Italy., Paolesse R; Department of Chemical Science and Technology, University of Rome Tor Vergata, 00133 Rome, Italy., Lopes HB; Bone Research Lab, School of Dentistry of Ribeirão Preto, University of São Paulo, 14040-904 Ribeirão Preto, Brazil., Beloti MM; Bone Research Lab, School of Dentistry of Ribeirão Preto, University of São Paulo, 14040-904 Ribeirão Preto, Brazil., Ciancaglini P; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil.; Department of Experimental Medicine, University of Rome Tor Vergata, 00133 Rome, Italy., Ramos AP; Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-900 Ribeirão Preto, Brazil., Bottini M; Department of Experimental Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.; Sanford Burnham Prebys, La Jolla, California 92037, United States. |
| Abstrakt: |
Tissue engineering offers attractive strategies to develop three-dimensional scaffolds mimicking the complex hierarchical structure of the native bone. The bone is formed by cells incorporated in a molecularly organized extracellular matrix made of an inorganic phase, called biological apatite, and an organic phase mainly made of collagen and noncollagenous macromolecules. Although many strategies have been developed to replicate the complexity of bone at the nanoscale in vitro , a critical challenge has been to control the orchestrated process of mineralization promoted by bone cells in vivo and replicate the anatomical and biological properties of native bone. In this study, we used type I collagen to fabricate mineralized scaffolds mimicking the microenvironment of the native bone. The sulfated polysaccharide κ-carrageenan was added to the scaffolds to fulfill the role of noncollagenous macromolecules in the organization and mineralization of the bone matrix and cell adhesion. Scanning electron microscopy images of the surface of the collagen/κ-carrageenan scaffolds showed the presence of a dense and uniform network of intertwined fibrils, while images of the scaffolds' lateral sides showed the presence of collagen fibrils with a parallel alignment, which is characteristic of dense connective tissues. MC3T3-E1 osteoblasts were cultured in the collagen scaffolds and were viable after up to 7 days of culture, both in the absence and in the presence of κ-carrageenan. The presence of κ-carrageenan in the collagen scaffolds stimulated the maturation of the cells to a mineralizing phenotype, as suggested by the increased expression of key genes related to bone mineralization, including alkaline phosphatase ( Alp ), bone sialoprotein ( Bsp ), osteocalcin ( Oc ), and osteopontin ( Opn ), as well as the ability to mineralize the extracellular matrix after 14 and 21 days of culture. Taken together, the results described in this study shed light on the potential use of collagen/κ-carrageenan scaffolds to study the role of the structural organization of bone-mimetic synthetic matrices in cell function. |
