The Rheumatology Division at Washington University requests continuation of a Rheumatic Diseases Core Center (RDCC). The overall goal of the RDCC is to provide an environment that will markedly enhance multidisciplinary study of rheumatic diseases by addressing the following overall Specific Aims: 1) Support core facilities to enhance funded, ongoing research that is relevant to the rheumatic diseases;2) Facilitate direct research on these diseases;3) Enhance interest in the rheumatic diseases;and 4) Foster development of junior faculty. The RDCC takes advantage of the very strong basic immunology research base in the Rheumatology Division and the wealth of expertise in other departments, especially in immunology and bone biology. In the previous funding period, the RDCC expanded services of existing core facilities at Washington University and established totally new core laboratories that enhance research relevant to the rheumatic diseases. The RDCC consists of an Administrative Core that will direct operations of the RDCC and will be aided by a Core Center Committee composed of senior faculty and outside advisors. An enrichment program supports outside speakers for seminars in relevant rheumatic disease research. Plans are outlined to support and enhance a Protein Core Facility to produce new monoclonal antibodies (mAbs) and produce and purify mAbs and recombinant proteins to help investigators analyze rheumatic disease models. The Genetics Core will be supported to produce transgenic and knockout mice production and facilitate production of backcrossed mice by the use of a """"""""speed congenics"""""""" approach. These services will ease investigation of rheumatic disease models that are genetically modified. A Pilot and Feasibility Program will support new studies from two junior faculty members who will work on projects involved in basic mechanisms of immune responses. Thus, the RDCC will provide not only a means to enhance ongoing research but also is organized in a manner to facilitate efforts of investigators in their study of rheumatic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR048335-10
Application #
7918819
Study Section
Special Emphasis Panel (ZAR1-EHB-D (O1))
Program Officer
Mancini, Marie
Project Start
2001-09-28
Project End
2011-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
10
Fiscal Year
2010
Total Cost
$590,368
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Yokoyama, Christine C; Baldridge, Megan T; Leung, Daisy W et al. (2018) LysMD3 is a type II membrane protein without an in vivo role in the response to a range of pathogens. J Biol Chem 293:6022-6038
Wu, Xiaobo; Hutson, Irina; Akk, Antonina M et al. (2018) Contribution of Adipose-Derived Factor D/Adipsin to Complement Alternative Pathway Activation: Lessons from Lipodystrophy. J Immunol 200:2786-2797
Kulkarni, Hrishikesh S; Liszewski, M Kathryn; Brody, Steven L et al. (2018) The complement system in the airway epithelium: An overlooked host defense mechanism and therapeutic target? J Allergy Clin Immunol 141:1582-1586.e1
Triebwasser, Michael P; Wu, Xiaobo; Bertram, Paula et al. (2018) Timing and mechanism of conceptus demise in a complement regulatory membrane protein deficient mouse. Am J Reprod Immunol 80:e12997
Roberson, Elisha D O (2018) Motif scraper: a cross-platform, open-source tool for identifying degenerate nucleotide motif matches in FASTA files. Bioinformatics 34:3926-3928
Paing, May M; Salinas, Nichole D; Adams, Yvonne et al. (2018) Shed EBA-175 mediates red blood cell clustering that enhances malaria parasite growth and enables immune evasion. Elife 7:
Wilke, Georgia; Ravindran, Soumya; Funkhouser-Jones, Lisa et al. (2018) Monoclonal Antibodies to Intracellular Stages of Cryptosporidium parvum Define Life Cycle Progression In Vitro. mSphere 3:
Kulkarni, Hrishikesh S; Elvington, Michelle L; Perng, Yi-Chieh et al. (2018) Intracellular C3 Protects Human Airway Epithelial Cells from Stress-Associated Cell Death. Am J Respir Cell Mol Biol :
Garber, Charise; Vasek, Michael J; Vollmer, Lauren L et al. (2018) Astrocytes decrease adult neurogenesis during virus-induced memory dysfunction via IL-1. Nat Immunol 19:151-161
Knoop, Kathryn A; Gustafsson, Jenny K; McDonald, Keely G et al. (2017) Microbial antigen encounter during a preweaning interval is critical for tolerance to gut bacteria. Sci Immunol 2:

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