The Yale Rheumatic Diseases Research Core Center (YRDRCC) comprises 44 investigators committed to understanding the etiology and pathogenesis of rheumatic diseases. The YRDRCC will provide Cores to enhance the productivity of these laboratories, to facilitate scientific exchange, and to provide access to state-of-the-art technology and unique resources (both within and outside of Yale) that would otherwise be unavailable. A great strength of our center is the broad and deep record of contributions of the investigators to rheumatic diseases and related research, making a compelling case for enhancing their productivity and capabilities. The interests of YRDRCC investigators ranges from basic mechanisms in central and peripheral immune tolerance, to Lyme disease, to the role of Toll-like receptors and NF-kB in inflammation and autoimmunity, to signaling defects in lymphocytes of lupus. The following Cores will be constituted: A) An Administrative Core to promote collaborations, scientific exchange, and education of new and established investigators in the field of rheumatic diseases;B) A Generation and Preservation of Novel Mouse Models Core to provide cryopreservation and reconstitution of frozen embryos for the cost-effective storage, safekeeping and distribution of genetically modified mice, of which YRDRCC investigators have a unique collection. To extend the capability to make next-generation genetically engineered mice to a wider group of investigators, the core will also provide technological expertise in the generation of knockout (KO), conditional KO, knock-in, and bacterial artificial chromosome (BAC) transgenic mice;C) An Intravital Microscopy Core to provide support for imaging fluorescently tagged cells within live anesthetized animals, using laser scanning multiphoton microscopy;and 4) A Luminex Bioassay Core to utilize Luminex beadbased technology, a flexible and sensitive methodology to analyze multiple interactions in a single microtiter assay. The YRDRCC is committed to supporting the careers of junior faculty investigators in the rheumatic diseases and to attract new investigators to the field. The four initial pilot and feasibility grants indicate this commitment, which will be ongoing. The combination of unique and useful Cores, a highly collaborative and productive group of senior investigators, and a promising cohort of junior investigators, comprises a very strong Center that should enable its investigators to make important contributions to the field.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR053495-05
Application #
8127775
Study Section
Special Emphasis Panel (ZAR1-KM-K (M1))
Program Officer
Mancini, Marie
Project Start
2007-08-17
Project End
2012-08-31
Budget Start
2011-08-01
Budget End
2012-08-31
Support Year
5
Fiscal Year
2011
Total Cost
$655,267
Indirect Cost
Name
Yale University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Gonzalez, David G; Cote, Christine M; Patel, Jaymin R et al. (2018) Nonredundant Roles of IL-21 and IL-4 in the Phased Initiation of Germinal Center B Cells and Subsequent Self-Renewal Transitions. J Immunol 201:3569-3579
Manfredo Vieira, S; Hiltensperger, M; Kumar, V et al. (2018) Translocation of a gut pathobiont drives autoimmunity in mice and humans. Science 359:1156-1161
Greiling, Teri M; Dehner, Carina; Chen, Xinguo et al. (2018) Commensal orthologs of the human autoantigen Ro60 as triggers of autoimmunity in lupus. Sci Transl Med 10:
Kim, Sang Taek; Choi, Jin-Young; Lainez, Begona et al. (2018) Human Extrafollicular CD4+ Th Cells Help Memory B Cells Produce Igs. J Immunol 201:1359-1372
Weinstein, Jason S; Laidlaw, Brian J; Lu, Yisi et al. (2018) STAT4 and T-bet control follicular helper T cell development in viral infections. J Exp Med 215:337-355
Fistonich, Chris; Zehentmeier, Sandra; Bednarski, Jeffrey J et al. (2018) Cell circuits between B cell progenitors and IL-7+ mesenchymal progenitor cells control B cell development. J Exp Med 215:2586-2599
Gies, Vincent; Schickel, Jean-Nicolas; Jung, Sophie et al. (2018) Impaired TLR9 responses in B cells from patients with systemic lupus erythematosus. JCI Insight 3:
Ip, W K Eddie; Hoshi, Namiko; Shouval, Dror S et al. (2017) Anti-inflammatory effect of IL-10 mediated by metabolic reprogramming of macrophages. Science 356:513-519
Swartz, Kelsey L; Wood, Scott N; Murthy, Tushar et al. (2017) E2F-2 Promotes Nuclear Condensation and Enucleation of Terminally Differentiated Erythroblasts. Mol Cell Biol 37:
Di Pietro, Caterina; Zhang, Ping-Xia; O'Rourke, Timothy K et al. (2017) Ezrin links CFTR to TLR4 signaling to orchestrate anti-bacterial immune response in macrophages. Sci Rep 7:10882

Showing the most recent 10 out of 88 publications