The proposed UCSF Core Center for Musculoskeletal Biology in Medicine (CCMBM) will be an interdisciplinary consortium of thirty-nine basic and clinical scientists dedicated to understanding the biology and pathophysiology of musculoskeletal disease. The goal is to stimulate and support transdisciplinary collaborations amongst existing, premier research programs at UCSF in order to accelerate translational research in osteoporosis and osteoarthritis. A fundamental challenge for bench-to-bedside translational research is the need to validate in humans the findings from small animal models. The proposed CCMBM will overcome this obstacle by forming a linkage between scientists who study disease biology, researchers who analyze vast archives of clinical data, and practitioners who actively treat patients. The UCSF CCMBM proposes three cores: 1) Skeletal Biology Core;2) Musculoskeletal and Quantitative Imaging Core;and 3) Epidemiology and Biostatistics Core. These cores will provide research support and technical training, as well as a venue for new collaborations and an entry point for new members. The Center will also foster scientific exchange through an Enrichment Program;the curriculum includes a monthly seminar featuring local and visiting scientists, an annual full-day retreat with the External Advisory board, and a quarterly half-day symposium with a rotating topic relevant to osteoporosis and osteoarthritis. Another vital component of the Center is its Pilot/Feasibility Program. This provides seed money to junior investigators and to scientists new to musculoskeletal research. Finally, the Tool and Technology Grant Program will provide funds to Center members for the purpose of utilizing the outstanding specialized research services available outside the CCMBM at UCSF. Overall, the funding base for the proposed CCMBM is robust, support from UCSF is strong, and opportunities for interactions within and outside the Center are numerous. The object of the Center is to make optimum use of all available resources to catalyze discovery in the basic biology of musculoskeletal disease.

Public Health Relevance

A goal of the proposed CCMBM is to facilitate translating laboratory advances to the diagnosis and treatment of human musculoskeletal disease. It is organized in a manner to reflect the spirit of the broad, interdisciplinary mandate of NIAMS: to develop cross-cutting research that integrates many disciplines and involves the interplay and collaboration of a diverse array of specialists from both basic and clinical areas.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
1P30AR066262-01
Application #
8693342
Study Section
Special Emphasis Panel (ZAR1)
Program Officer
Tyree, Bernadette
Project Start
2014-07-01
Project End
2019-06-30
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Orthopedics
Type
Schools of Medicine
DUNS #
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Amano, Keiko; Huebner, Janet L; Stabler, Thomas V et al. (2018) Synovial Fluid Profile at the Time of Anterior Cruciate Ligament Reconstruction and Its Association With Cartilage Matrix Composition 3 Years After Surgery. Am J Sports Med 46:890-899
Kazakia, Galateia J; Carballido-Gamio, Julio; Lai, Andrew et al. (2018) Trabecular bone microstructure is impaired in the proximal femur of human immunodeficiency virus-infected men with normal bone mineral density. Quant Imaging Med Surg 8:5-13
Magnitsky, Sergey; Dudli, Stefan; Tang, Xinyan et al. (2018) Quantification of Propionic Acid in the Bovine Spinal Disk After Infection of the Tissue With Propionibacteria acnes Bacteria. Spine (Phila Pa 1976) 43:E634-E638
Barruet, Emilie; Morales, Blanca M; Cain, Corey J et al. (2018) NF-?B/MAPK activation underlies ACVR1-mediated inflammation in human heterotopic ossification. JCI Insight 3:
Berg-Johansen, Britta; Jain, Deeptee; Liebenberg, Ellen C et al. (2018) Tidemark Avulsions are a Predominant Form of Endplate Irregularity. Spine (Phila Pa 1976) 43:1095-1101
Davies, Michael R; Garcia, Steven; Tamaki, Stanley et al. (2018) Muscle stem cell activation in a mouse model of rotator cuff injury. J Orthop Res 36:1370-1376
Alemi, A Sean; Mazur, Courtney M; Fowler, Tristan W et al. (2018) Glucocorticoids cause mandibular bone fragility and suppress osteocyte perilacunar-canalicular remodeling. Bone Rep 9:145-153
Ford, Audrey C; Chui, Wan Fung; Zeng, Anne Y et al. (2018) A modular approach to creating large engineered cartilage surfaces. J Biomech 67:177-183
Berg-Johansen, Britta; Han, Misung; Fields, Aaron J et al. (2018) Cartilage Endplate Thickness Variation Measured by Ultrashort Echo-Time MRI Is Associated With Adjacent Disc Degeneration. Spine (Phila Pa 1976) 43:E592-E600
Sampson, Sara L; Sylvia, Meghan; Fields, Aaron J (2018) Effects of dynamic loading on solute transport through the human cartilage endplate. J Biomech :

Showing the most recent 10 out of 54 publications