8 results on '"Pompo, Gemma di"'
Search Results
2. Effect of calcium phosphate heparinization on the in vitro inflammatory response and osteoclastogenesis of human blood precursor cells
- Author
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Universitat Politècnica de Catalunya. Departament de Ciència i Enginyeria de Materials, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Uppsala universitet, Università di Bologna, Institut de Bioenginyeria de Catalunya, Díez Escudero, Anna, Torreggiani, E., Pompo, Gemma di, Español Pons, Montserrat, Persson, Cecilia, Ciapetti, Gabriela, Baldini, Nicola, Ginebra Molins, Maria Pau, Universitat Politècnica de Catalunya. Departament de Ciència i Enginyeria de Materials, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Uppsala universitet, Università di Bologna, Institut de Bioenginyeria de Catalunya, Díez Escudero, Anna, Torreggiani, E., Pompo, Gemma di, Español Pons, Montserrat, Persson, Cecilia, Ciapetti, Gabriela, Baldini, Nicola, and Ginebra Molins, Maria Pau
- Abstract
The immobilization of natural molecules on synthetic bone grafts stands as a strategy to enhance their biological interactions. During the early stages of healing, immune cells and osteoclasts (OC) modulate the inflammatory response and resorb the biomaterial, respectively. In this study, heparin, a naturally occurring molecule in the bone extracellular matrix, was covalently immobilized on biomimetic calcium-deficient hydroxyapatite (CDHA). The effect of heparin-functionalized CDHA on inflammation and osteoclastogenesis was investigated using primary human cells and compared with pristine CDHA and beta-tricalcium phosphate (ß-TCP). Biomimetic substrates led to lower oxidative stresses by neutrophils and monocytes than sintered ß-TCP, even though no further reduction was induced by the presence of heparin. In contrast, heparinized CDHA fostered osteoclastogenesis. Optical images of stained TRAP positive cells showed an earlier and higher presence of multinucleated cells, compatible with OC at 14 days, while pristine CDHA and ß-TCP present OC at 21–28 days. Although no statistically significant differences were found in the OC activity, microscopy images evidenced early stages of degradation on heparinized CDHA, compatible with osteoclastic resorption. Overall, the results suggest that the functionalization with heparin fostered the formation and activity of OC, thus offering a promising strategy to integrate biomaterials in the bone remodelling cycle by increasing their OC-mediated resorption., Peer Reviewed, Postprint (author's final draft)
- Published
- 2019
3. Osteoclast differentiation from human blood precursors on biomimetic calcium-phosphate substrates
- Author
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Universitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Ciapetti, Gabriela, Pompo, Gemma di, Avnet, Sofia, Martini, Desirée, Díez Escudero, Anna, Montufar Jiménez, Edgar Benjamin, Ginebra Molins, Maria Pau, Baldini, Nicola, Universitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Ciapetti, Gabriela, Pompo, Gemma di, Avnet, Sofia, Martini, Desirée, Díez Escudero, Anna, Montufar Jiménez, Edgar Benjamin, Ginebra Molins, Maria Pau, and Baldini, Nicola
- Abstract
The design of synthetic bone grafts to foster bone formation is a challenge in regenerative medicine. Understanding the interaction of bone substitutes with osteoclasts is essential, since osteoclasts not only drive a timely resorption of the biomaterial, but also trigger osteoblast activity. In this study, the adhesion and differentiation of human blood-derived osteoclast precursors (OCP) on two different micro-nanostructured biomimetic hydroxyapatite materials consisting in coarse (HA-C) and fine HA (HA-F) crystals, in comparison with sintered stoichiometric HA (sin-HA, reference material), were investigated. Osteoclasts were induced to differentiate by RANKL-containing supernatant using cell/substrate direct and indirect contact systems, and calcium (Ca++) and phosphorus (P5+) in culture medium were measured. We observed that OCP adhered to the experimental surfaces, and that osteoclast-like cells formed at a rate influenced by the micro- and nano-structure of HA, which also modulate extracellular Ca++. Qualitative differences were found between OCP on biomimetic HA-C and HA-F and their counterparts on plastic and sin-HA. On HA-C and HA-F cells shared typical features of mature osteoclasts, i.e. podosomes, multinuclearity, tartrate acid phosphatase (TRAP)-positive staining, and TRAP5b-enzyme release. However, cells were less in number compared to those on plastic or on sin-HA, and they did not express some specific osteoclast markers. In conclusion, blood-derived OCP are able to attach to biomimetic and sintered HA substrates, but their subsequent fusion and resorptive activity are hampered by surface micro-nano-structure. Indirect cultures suggest that fusion of OCP is sensitive to topography and to extracellular calcium., Preprint
- Published
- 2017
4. Focus ion beam/scanning electron microscopy characterization of osteoclastic resorption of calcium phosphate substrates
- Author
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Universitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Díez Escudero, Anna, Español Pons, Montserrat, Montufar Jiménez, Edgar Benjamin, Pompo, Gemma di, Ciapetti, Gabriela, Baldini, Nicola, Ginebra Molins, Maria Pau, Universitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica, Universitat Politècnica de Catalunya. BBT - Biomaterials, Biomecànica i Enginyeria de Teixits, Istituto Ortopedico Rizzoli, Díez Escudero, Anna, Español Pons, Montserrat, Montufar Jiménez, Edgar Benjamin, Pompo, Gemma di, Ciapetti, Gabriela, Baldini, Nicola, and Ginebra Molins, Maria Pau
- Abstract
This article presents the application of dual focused ion beam/scanning electron microscopy (FIB-SEM) imaging for preclinical testing of calcium phosphates with osteoclast precursor cells and how this high-resolution imaging technique is able to reveal microstructural changes at a level of detail previously not possible. Calcium phosphate substrates, having similar compositions but different microstructures, were produced using low- and high-temperature processes (biomimetic calcium-deficient hydroxyapatite [CDHA] and stoichiometric sintered hydroxyapatite, respectively). Human osteoclast precursor cells were cultured for 21 days before evaluating their resorptive potential on varying microstructural features. Alternative to classical morphological evaluation of osteoclasts (OC), FIB-SEM was used to observe the subjacent microstructure by transversally sectioning cells and observing both the cells and the substrates. Resorption pits, indicating OC activity, were visible on the smoother surface of high-temperature sintered hydroxyapatite. FIB-SEM analysis revealed signs of acidic degradation on the grain surface under the cells, as well as intergranular dissolution. No resorption pits were evident on the surface of the rough CDHA substrates. However, whereas no degradation was detected by FIB sections in the material underlying some of the cells, early stages of OC-mediated acidic degradation were observed under cells with more spread morphology. Collectively, these results highlight the potential of FIB to evaluate the resorptive activity of OC, even in rough, irregular, or coarse surfaces where degradation pits are otherwise difficult to visualize., Peer Reviewed, Postprint (author's final draft)
- Published
- 2017
5. MCT1 as a novel target for the treatment of osteolytic bone metastases
- Author
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Paolo E. Porporato, Martina Sboarina, Nicola Baldini, Pompo Gemma Di, Pierre Sonveaux, Sofia Avnet, Silvia Lemma, and Jhudit Pérez-Escuredo
- Subjects
General Medicine - Published
- 2016
- Full Text
- View/download PDF
6. The effect of potassium citrate on human primary osteoclasts in vitro
- Author
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Nicola Baldini, Elena Torreggiani, Donatella Granchi, Annamaria Massa, and Pompo Gemma Di
- Subjects
Primary (chemistry) ,Biochemistry ,chemistry ,Potassium ,chemistry.chemical_element ,General Medicine ,In vitro - Published
- 2016
- Full Text
- View/download PDF
7. The role of acidic microenvironment in the context of osteolytic carcinomas
- Author
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Nicola Baldini, Silvia Lemma, Lorenzo Canti, Pompo Gemma Di, Robert J. Gillies, and Sofia Avnet
- Subjects
Cancer research ,Context (language use) ,General Medicine ,Biology - Published
- 2016
- Full Text
- View/download PDF
8. Advantages and limitations of using cell viability assays for 3D bioprinted constructs.
- Author
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Avnet S, Pompo GD, Borciani G, Fischetti T, Graziani G, and Baldini N
- Subjects
- Cell Survival, Spheroids, Cellular, Alginates, Bone and Bones, Gelatin, Printing, Three-Dimensional, Tissue Scaffolds, Tissue Engineering methods, Hydrogels, Bioprinting methods
- Abstract
Bioprinting shows promise for bioengineered scaffolds and three-dimensional (3D) disease models, but assessing the viability of embedded cells is challenging. Conventional assays are limited by the technical problems that derive from using multi-layered bioink matrices dispersing cells in three dimensions. In this study, we tested bioprinted osteogenic bioinks as a model system. Alginate- or gelatin-based bioinks were loaded with/without ceramic microparticles and osteogenic cells (bone tumor cells, with or without normal bone cells). Despite demonstrating 80%-90% viability through manual counting and live/dead staining, this was time-consuming and operator-dependent. Moreover, for the alginate-bioprinted scaffold, cell spheroids could not be distinguished from single cells. The indirect assay (alamarBlue), was faster but less accurate than live/dead staining due to dependence on hydrogel permeability. Automated confocal microscope acquisition and cell counting of live/dead staining was more reproducible, reliable, faster, efficient, and avoided overestimates compared to manual cell counting by optical microscopy. Finally, for 1.2 mm thick 3D bioprints, dual-photon confocal scanning with vital staining greatly improved the precision of the evaluation of cell distribution and viability and cell-cell interactions through the z -axis. In summary, automated confocal microscopy and cell counting provided superior accuracy for the assessment of cell viability and interactions in 3D bioprinted models compared to most commonly and currently used techniques., (Creative Commons Attribution license.)
- Published
- 2024
- Full Text
- View/download PDF
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