This is a competing renewal application for the Rheumatic Diseases Core Center (RDCC) at Washington University. The overall goal of the RDCC is to enhance multidisciplinary study of the rheumatic diseases. To achieve these goals, the following Specific Aims are proposed: 1) Support ongoing funded research;2) Facilitate direct study of rheumatic disease models;3) Enhance interest in the rheumatic diseases;4) Expedite translational research in the rheumatic diseases (a new Specific Aim);and 5) Foster development of junior faculty. To address these Specific Aims, an Administrative Core is proposed to provide leadership, management, and infrastructure. An Enrichment Program is proposed consisting of outside speaker support, and a Pilot and Feasibility (P/F) Program in which projects by junior faculty are supported. Two research cores are proposed. A Genetics Core will consist of a Transgenic and Knockout Mouse Facility, a Speed Congenics Facility, and a new Human Genomics and Bioinformatics Facility. A Protein Core will consist of a Hybridoma Center, and a Protein Production and Purification Facility. Over the current funding period, these cores have demonstrated productivity and are testing new protocols that are now ready for use by RDCC investigators. All core facilities propose to test additional services that will be added in the future. Thus, the RDCC will provide not only a means to enhance ongoing research but also is organized in a manner to facilitate the 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 #
5P30AR048335-13
Application #
8528467
Study Section
Special Emphasis Panel (ZAR1-MLB (M1))
Program Officer
Mao, Su-Yau
Project Start
2001-09-28
Project End
2016-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
13
Fiscal Year
2013
Total Cost
$577,602
Indirect Cost
$197,601
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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
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
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:

Showing the most recent 10 out of 156 publications