? Resource Core 2: Cellular Systems Core Investigators in the Joint Biology Consortium (JBC) share a set of technical challenges that impede utilization of state-of-the-art human and murine cell analysis for arthritis research. To overcome these hurdles, the Cellular Systems Core (CSC) will leverage economies of scale to develop an integrated set of research tools to serve JBC members across 17 centers. The CSC will provide four distinct but interrelated services. First, the Brigham and Women's Human Immunology Center will become the central collection and processing site for human samples, enabling not only logistically simplified collection but also specialized handling of synovial tissues as well as cells intended for high-resolution single-cell analysis. Second, the CSC will support optimized cytometry by time of flight (CyTOF), including arthritis-related antibody panels, rare earth metal conjugation, barcoding, and data analysis. Third, the CSC will simplify access to single-cell and low-input RNA-seq through the Broad Institute, including first access to Drop-seq and related methods and analysis. Finally, recognizing the ongoing importance of murine translation for pre-clinical research, the CSC will provide centralized development and CRISPR/Cas9 genetic manipulation of experimental model cells using innovative HoxB8 technology, ideal for in vitro and in vivo investigation of the biology of cells lineages including neutrophils, monocyte and osteoclasts. Progressive optimization of CSC services will result not only from JBC member studies but, importantly, through technical coordination with the Accelerating Medicines Partnership (AMP) in arthritis research, ensuring that JBC members have access to the latest methodologic advances. Service delivery will be led by a senior scientific team consisting of Harvard CyTOF director Dr. James Lederer, supported by associate directors Dr. Chad Nusbaum of the Broad Technology Labs and Dr. Peter Nigrovic at BWH/Children's. This team will ensure that the logistical investment represented by the Cellular Systems Core will accelerate innovative translational arthritis research within the JBC.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
1P30AR070253-01
Application #
9162780
Study Section
Special Emphasis Panel (ZAR1-YL (M1))
Project Start
Project End
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
$293,847
Indirect Cost
$124,002
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Lee, Pui Y; Huang, Yuelong; Zhou, Qing et al. (2018) Disrupted N-linked glycosylation as a disease mechanism in deficiency of ADA2. J Allergy Clin Immunol 142:1363-1365.e8
Li, Gang; Martínez-Bonet, Marta; Wu, Di et al. (2018) High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction. Nat Genet 50:1180-1188
Vastert, Sebastiaan J; Nigrovic, Peter A (2018) Editorial: Toward Personalized Treatment for Systemic Juvenile Idiopathic Arthritis. Arthritis Rheumatol 70:1172-1174
Sparks, Jeffrey A; Barbhaiya, Medha; Tedeschi, Sara K et al. (2018) Inflammatory dietary pattern and risk of developing rheumatoid arthritis in women. Clin Rheumatol :
Mizoguchi, Fumitaka; Slowikowski, Kamil; Wei, Kevin et al. (2018) Functionally distinct disease-associated fibroblast subsets in rheumatoid arthritis. Nat Commun 9:789
Sparks, Jeffrey A; Lin, Tzu-Chieh; Camargo Jr, Carlos A et al. (2018) Rheumatoid arthritis and risk of chronic obstructive pulmonary disease or asthma among women: A marginal structural model analysis in the Nurses' Health Study. Semin Arthritis Rheum 47:639-648
Kreps, David J; Halperin, Florencia; Desai, Sonali P et al. (2018) Association of weight loss with improved disease activity in patients with rheumatoid arthritis: A retrospective analysis using electronic medical record data. Int J Clin Rheumtol 13:1-10
Prado, Maria G; Iversen, Maura D; Yu, Zhi et al. (2018) Effectiveness of a Web-Based Personalized Rheumatoid Arthritis Risk Tool With or Without a Health Educator for Knowledge of Rheumatoid Arthritis Risk Factors. Arthritis Care Res (Hoboken) 70:1421-1430
Nigrovic, Peter A; Raychaudhuri, Soumya; Thompson, Susan D (2018) Review: Genetics and the Classification of Arthritis in Adults and Children. Arthritis Rheumatol 70:7-17
Sparks, Jeffrey A; Iversen, Maura D; Yu, Zhi et al. (2018) Disclosure of Personalized Rheumatoid Arthritis Risk Using Genetics, Biomarkers, and Lifestyle Factors to Motivate Health Behavior Improvements: A Randomized Controlled Trial. Arthritis Care Res (Hoboken) 70:823-833

Showing the most recent 10 out of 40 publications