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Researchers of NANBIOSIS U3 find activators of a possible therapeutic target for the treatment of patients with diabetes and insulin resistance

Researchers of  NANBIOSIS U3: Synthesis of Peptides Unit participate in the identification of activators of of the mitochondrial protein Mitofusin 2, a possible therapeutic target for the treatment of patients with type 2 diabetes in collaboration with CIBER of Diabetes and Associated Metabolic Diseases (CIBERDEM) and the CIBER of Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN).

Those researchers are led by Fernando Albericio (Scientific Director of Unit 3 of NANBIOSIS) at the University of Barcelona and Antonio Zorzano en el IRB Barcelona  have identified activators of the mitochondrial protein Mitofusin 2 for the treatment of type 2 diabetes. This protein is expressed at abnormally low levels in the tissues of patients with diabetes. “Thanks to the studies of phenotypic screening and validation studies in human cells, it has been possible to demonstrate the role of the protein Mitofusin 2 in the development of many of the alterations associated with diabetes”, explain those responsible for the work.

These studies have been possible thanks to the work of biologists and chemists from different CIBER areas and with experience in synthetic chemistry, molecular screening and functional analysis.

Article of reference:

Identification of New Activators of Mitochondrial Fusion Reveals a Link between Mitochondrial Morphology and Pyrimidine Metabolism. Miret-Casals L, Sebastián D, Brea J, Rico-Leo EM, Palacín M, Fernández-Salguero PM, Loza MI, Albericio F, Zorzano A. Cell Chem Biol. 2017 Dec 23. pii: S2451-9456(17)30428-2. doi: 10.1016/j.chembiol.2017.12.001.

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José Luis Pedraz, Scientific Director of the Unit 10: Drug Formulation of NANBIOSIS explained DRIVE European project in the third edition of Diabetes Experience Day, diabetic patients meeting that gathered 1500 people in Madrid. The DRIVE project, in which participate fourteen partners from seven European countries, among which is the CIBER-BBN, develops biomaterials and new surgical devices to improve transplantation and survival of insulin-producing pancreatic islet for the treatment diabetes.

 

The DRIVE project, in which participate fourteen partners from seven European countries, among which is the CIBER-BBN, develops biomaterials and new surgical devices to improve transplantation and survival of insulin-producing pancreatic islet for the treatment diabetes.

NANBIOSIS participation in the project focuses on the evaluation of the biocompatibility of new biomaterials with insulin-producing cells. These new biomaterials provided by Contipro will be compared with the biomaterials most frequently used to encapsulate cells such as alginate derivatives, a product obtained from seaweed.

At the same time, the research group coordinating Unit 10 of NANBIOSIS work in differentiating IPC insulin producing cells as an alternative to pancreatic islets for use in bioartificial organ source, with the aim of addressing the problems of availability of pancreatic islets for such therapies.

DRIVE European project 3rd edition of  Diabetes Experience Day.

Nanbiosis_Unit8-Drive Project-Improving transplant pancreatic cells_Dr. Jose Luis Pedraz
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CIBER-BBN, partner in the DRIVE project to develop biomaterials and Cell based treatments for diabetes

The CIBER-BBN is partner in a new EU consortium which receives €8.9 million funding to develop materials and cell based treatments for diabetes

Programme of research will be a game-changer for people with Type 1 diabetes and insulin-dependent Type 2 diabetes

Last June took place in Brussels the kick-off meeting of the European project DRIVE (Diabetes Reversing Implants with enhanced Viability and long-term Efficacy), consortium involves fourteen partners from seven European countries, has received €8.9 million funding as part of the Horizon 2020 – Research and Innovation Framework Programme.

The DRIVE programme will develop natural materials and new surgical devices to enhance the transplant and survival of insulin producing pancreatic islets for the treatment of diabetes. DRIVE project is co-ordinated by Dr. Garry Duffy, Department of Anatomy and Tissue Engineering Research Group, Royal College of Surgeons in Ireland. Prof. José Luis Pedraz, led of the Nanobiocel Group of CIBER-BBN in the Universidad del País Vasco (UPV/EHU) and coordinator of the Unit 10-Drug Formulation of NANBIOSIS, participates in this consortium.

Drive Project kick-off meeting

Drive Project kick-off meeting

Diabetes mellitus is a chronic disease characterised by high blood sugar (glucose).  If not treated carefully, diabetes causes several debilitating side effects including heart disease, damage to the eyes, kidneys and nerve endings (e.g. hands, feet) and can lead to premature death. The total number of people living with diabetes in Ireland is estimated to be over 225,000.  According to the international diabetes federation (IDF), 382 million people worldwide have diabetes and in 2013 an estimated 5.1 million deaths were attributable to the disease, representing 8.4% of global adult mortality. Blood glucose is high in diabetes because of the inability of the pancreas to produce sufficient insulin, a hormone that controls blood sugar. Currently the main treatment for diabetes is the daily injection of insulin. In patients where control is poor, transplantation of pancreatic cells (which contain insulin-producing β-cells) is possible. However there are challenges with this therapy including the short supply of donor pancreases, the need to use 3-4 pancreases to get enough β-cells for treatment and poor graft survival and retention at the transplant site.

The DRIVE consortium will address these challenges by developing a completely new system to deliver pancreatic β-cells effectively in a targeted and protected fashion. This will mean that fewer donor pancreases are needed for cell transplantation allowing more patients to avail of a more effective longer-lasting treatment with less demand on donor pancreases. Additionally, the consortium will investigate the combination of DRIVE’s technology with future stem cell-derived β-cells that will widen the availability of islet transplantation therapy to all insulin-dependent patients.

Dr. José Luis Pedraz, commented on the research funding: “We are delighted to participate in the DRIVE programme to translate new collaborative research for the benefit of patients with diabetes mellitus.  Regenerative medicine and stem cell therapies have the potential to revolutionise the treatment of patients who have diabetes, and through DRIVE we will develop new technologies to enhance stem cell therapies for these patients by increasing targeting and ease of delivery using advanced biomaterials.”

DRIVE’s β-System consists of a β-Gel, which contains the pancreatic β-cells within a pancreas mimicking gel; which itself is protected within a capsule called a β-shell. This is delivered using a specialised injection catheter, called β-cath, which offers a more minimally invasive surgical procedure than is currently used.

The current transplantation technique offers patients natural glucose control for 1-2 years. DRIVE’s β-system aims to provide control for up to 5 years by increasing the longevity of the β-cell transplant. The system offers further advantages through the slow release of immunosuppressant drugs by the β-shell, reducing the patient’s need for long-term anti-rejection medication, which has harmful side effects. The β-shell will also be retrievable, so it can be removed and replenished after the 5-year period. DRIVE’s 5-year work plan will include animal testing, with a view to human testing at the end of the project.

Professor Paul Johnson, Director of the Oxford Islet Transplant Programme and Professor of Paediatric Surgery at the University of Oxford, said: “Over the past 10 years, the transplantation of insulin-producing pancreatic cells known as islet cells (that can sense blood sugar levels and release insulin to maintain normal sugar levels) has achieved very promising results in adults who have developed the severest complications from insulin-dependent diabetes. The challenge is to now make sure that more people can benefit from this minimally-invasive treatment. Ultimately we would hope that it can be used to reverse diabetes in children soon after diagnosis. The DRIVE Consortium brings together some of the leading researchers in Europe in the fields of bioengineering, cell biology, and cell transplantation. The overall aim is to develop novel membranes to protect the transplanted islets from rejection ensure that islet transplantation can be undertaken without the need for the patient to take anti-rejection medication, with all the associated complications. This programme of research could be a real game-changer for people with Type 1 diabetes and the team in Oxford are very excited to be part of this state of the art research collaboration.”

The DRIVE Consortium represents a major interdisciplinary effort between stem cell biologists, experts in advanced drug delivery, research scientists, clinicians and research-active companies working together to develop novel therapeutics to address the challenges of treating diabtes. The researchers will optimise adult stem cell therapy using smart biomaterials and advanced drug delivery, and couple these therapeutics with minimally-invasive surgical devices.

Further Information about DRIVE

The project has recived funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement no 645991.

 Other partners include:

Royal College of Surgeon’s in Ireland (Ireland)

Dublin City University (Ireland)

Eberhard Karls University Tuebingen (Germany)

Utrecht University (The Netherlands)

University College Dublin (Ireland)

CIBER-BBN (Spain)

Abiel S.r.l. (Italy)

Contipro Pharma A.S.(Czech Republic)

Explora Biotech S.r.l. (Italy)

InnoCore Pharmaceuticals (The Netherlands)

Boston Scientific Ireland Ltd (Ireland)

INNOVA S.p.A. (Italy)

Ospedale Niguarda Ca’ Granda (Italy)

University of Oxford (UK)

Nanoencapsulated cells
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