Induced pluripotent stem cells (IPS cells), generated by transcription factor-dependent nuclear reprogramming of differentiated somatic cells, are pluripotent stem cell lines that can be propagated indefinitely in culture and maintain the potential to differentiate into any cell type in the body. As iPS cells retain the same genetic make-up as the somatic cell targeted for reprogramming, these cells hold tremendous promise for uncovering novel genetic and biochemical factors that underiie diseases with complex and pooriy understood genetic influences, such as diabetes. The DRC iPS Core will establish and maintain a centralized facility for the reliable and consistent generation and propagation of reprogrammed IPS cells for use in cutting-edge research into the molecular and cellular pathologies underiying diabetes and its complications. The Core will enhance the scientific productivity of DRC projects in multiple ways: (1) By standardizing medical assessments and data collection from human subjects, as well as cell isolation protocols and reagents, the Core will allow direct comparison of data across projects and remove variability resulting from potential technical or biological differences in patient populations or cell handling. (2) As IPS cell production and propagation can be technically challenging, the Core will ensure reproducibility and comparability of results, by enforcing rigorous standards of quality control. (3) The Core will provide advanced training for investigators desiring to introduce IPS technologies into their own laboratories, increasing the currently small number of laboratories in the Boston area skilled in the isolation and culture of IPS cells. (4) The Core will provide expert advice on experimental design, regulatory documentation and interpretation of results, based on the extensive expertise of the Core Directors and Staff. (5) As the Core will be utilized by multiple labs, it will provide a venue for scientific interaction, fostering greater exchange of information among DRC Investigators and promoting productive collaborations with other Boston-based research groups. (6) The Core will help to develop new technologies that support center activities, including most notably the optimization of methods for deriving iPS cells from people with diabetes and the integration of new reprogramming technologies, including integration-free IPS generation and generation ofiPS cells from peripheral blood samples, as these become robust and available. These activities will benefit DRC Investigators and significantly accelerate advances in diabetes research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK036836-26A1
Application #
8447675
Study Section
Special Emphasis Panel (ZDK1-GRB-S (O2))
Project Start
Project End
Budget Start
2012-09-14
Budget End
2013-08-31
Support Year
26
Fiscal Year
2012
Total Cost
$183,531
Indirect Cost
$72,244
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Mulla, Christopher M; Middelbeek, Roeland J W; Patti, Mary-Elizabeth (2018) Mechanisms of weight loss and improved metabolism following bariatric surgery. Ann N Y Acad Sci 1411:53-64
Skupien, Jan; Smiles, Adam M; Valo, Erkka et al. (2018) Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced Nephropathy. Diabetes Care :
Laffel, L (2018) Lost in transition: finding a path forward for young adults with Type 1 diabetes. Diabet Med 35:1061-1062
Rao, Tata Nageswara; Gupta, Manoj K; Softic, Samir et al. (2018) Attenuation of PKC? enhances metabolic activity and promotes expansion of blood progenitors. EMBO J 37:
Bauman, Viviana; Sturkey, Adaya C; Sherafat-Kazemzadeh, Rosa et al. (2018) Factitious hypoglycemia in children and adolescents with diabetes. Pediatr Diabetes 19:823-831
Stanford, Kristin I; Rasmussen, Morten; Baer, Lisa A et al. (2018) Paternal Exercise Improves Glucose Metabolism in Adult Offspring. Diabetes 67:2530-2540
Park, Kyoungmin; Li, Qian; Evcimen, Net Da? et al. (2018) Exogenous Insulin Infusion Can Decrease Atherosclerosis in Diabetic Rodents by Improving Lipids, Inflammation, and Endothelial Function. Arterioscler Thromb Vasc Biol 38:92-101
Lynes, Matthew D; Shamsi, Farnaz; Sustarsic, Elahu Gosney et al. (2018) Cold-Activated Lipid Dynamics in Adipose Tissue Highlights a Role for Cardiolipin in Thermogenic Metabolism. Cell Rep 24:781-790
Schuster, Cornelia; Jonas, Franziska; Zhao, Fangzhu et al. (2018) Peripherally induced regulatory T cells contribute to the control of autoimmune diabetes in the NOD mouse model. Eur J Immunol 48:1211-1216
Laguna Sanz, Alejandro J; Mulla, Christopher M; Fowler, Kristen M et al. (2018) Design and Clinical Evaluation of a Novel Low-Glucose Prediction Algorithm with Mini-Dose Stable Glucagon Delivery in Post-Bariatric Hypoglycemia. Diabetes Technol Ther 20:127-139

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