PEPTIDE OSTEOGEL

Determining novel peptide sequence and matrix mechanical properties to increase osteogenesis in embryonic stem cells using designer alginate hydrogels for bone regeneration

Coordinatore	IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE    more  Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD city: LONDON postcode: SW7 2AZ contact info Titolo: Mr. Nome: Shaun Cognome: Power Email: send email Telefono: +44 20 7594 8773 Fax: +44 20 7594 8609
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	201˙049 €
EC contributo	201˙049 €
Programma	FP7-PEOPLE Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
Code Call	FP7-PEOPLE-2010-IIF
Funding Scheme	MC-IIF
Anno di inizio	2011
Periodo (anno-mese-giorno)	2011-03-01   -   2013-02-28

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE  Organization address address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD city: LONDON postcode: SW7 2AZ contact info Titolo: Mr. Nome: Shaun Cognome: Power Email: send email Telefono: +44 20 7594 8773 Fax: +44 20 7594 8609	UK (LONDON)	coordinator	201˙049.60

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 Obiettivo del progetto (Objective)

'Regenerating large bone defects is a great challenge in regenerative medicine. Embryonic stem cell (ESC) therapies are an attractive option due to their unlimited proliferation and ability to produce the cell types needed for bone repair. Here, we propose creating a three-dimensional alginate hydrogel that displays bioactive epitopes and has mechanical properties that induce osteogenic differentiation of ESCs and increase bone formation in vitro. We will do this by building upon previous research in the group of Prof Molly Stevens, which found that ESCs cultured on the extracellular matrix of bone forming osteoblasts increased both differentiation into osteogenic cells and bone formation. We propose using a proteomic approach to identify the proteins that are responsible for this effect. Once the proteins are known, they will be cut into short overlapping peptides that will be synthesized and attached to a cell culture surface. ESCs will then be grown on them to determine the sequences that induce osteogenesis. Using two-dimensional hydrogels of different stiffness that are coated with the osteogenic peptide, the mechanical properties that maximize osteogenesis will be determined. This peptide will then be coupled to alginate to form a hydrogel whose mechanical properties will be tailored to maximize bone formation. Novel sequences which induce osteogenesis are important to stem cell biology and an artificial matrix that differentiates ESCs into osteoblasts using both displayed ligands and stiffness would be important to regenerative medicine. The project Peptide Osteogel will be beneficial to Europe by bringing a scientist with a unique skill set into a top biomaterials lab to work on a multidisciplinary project that will increase the quality and status of science in the European Union. This fellowship will enable greater collaboration and transfer of knowledge across Europe, increasing the mobility and human potential of scientists across the continent.'