The Molecular and Anatomic Imaging Core will be used extensively by both the clinical an basic science? components of all four of the projects. Utilization of the Core will be fairly equal among the four projects,? although the services used will vary somewhat depending on the project focus. In combining molecular? imaging and anatomic imaging under a single administrative structure, we have a unique opportunity not only? to support translation in the sense of basic science to clinical application, but also to enable translation? between molecular and anatomic imaging techniques, which can enhance both components. This will be? facilitated by the structure we propose, which will consist of the Core co-directors in Pathology and? Radiology who will oversee the molecular and anatomic services, respectively, as well as an internal? committee which will help to ensure coordination, communication and translation between these services.? The Core has 2 aims relating to provision of tissue-based molecular and clinical and animal anatomic? imaging studies. In addition, there will be 3 subaims for technological development within the molecular? component, and 3 subaims within the anatomic component, to develop new technologies and enhancements? which could accelerate progress in the Project specific aims, and generate new approaches for future? translational research.
The aims are: 1. Provision of high quality, efficient, and cost-effective tissue-based? molecular imaging studies. 2. Provision of high quality, consistent, efficient and cost-effective anatomic? imaging studies in mice and humans. 3. Technology enhancement and refinement to bring new cutting-edge? imaging technologies into basic and clinical research practice.
Aim 3 has 6 subaims:? Molecular Imaging Subaims: (A). Development of laser capture PCR for regional tissue gene expression? analysis on samples of cartilage and bone related to the Projects. (B) Development of a quantitative? methodology of evaluating signaling in cell culture using immunofluorescent confocal microscopy. (C)? Quantitative signaling evaluation in tissue samples of cartilage or fracture callus confocal.? Anatomic Imaging Subaims: (D) Development of software algorithms for clinical cone beam CT to quantify? fracture healing in the presence of hardware. (E) Use of microCT to quantitate murine joint articular cartilage? volumes. (F)Design of new micro-coils for high resolution MRI of mouse knee joints.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Specialized Center (P50)
Project #
5P50AR054041-03
Application #
7682124
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2008-08-01
Project End
2011-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
3
Fiscal Year
2008
Total Cost
$336,321
Indirect Cost
Name
University of Rochester
Department
Type
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Yukata, Kiminori; Xie, Chao; Li, Tian-Fang et al. (2018) Teriparatide (human PTH1-34) compensates for impaired fracture healing in COX-2 deficient mice. Bone 110:150-159
de Mesy Bentley, Karen L; Trombetta, Ryan; Nishitani, Kohei et al. (2017) Evidence of Staphylococcus Aureus Deformation, Proliferation, and Migration in Canaliculi of Live Cortical Bone in Murine Models of Osteomyelitis. J Bone Miner Res 32:985-990
Bez, Maxim; Sheyn, Dmitriy; Tawackoli, Wafa et al. (2017) In situ bone tissue engineering via ultrasound-mediated gene delivery to endogenous progenitor cells in mini-pigs. Sci Transl Med 9:
Zingman, Alissa; Li, Hiayan; Sundem, Leigh et al. (2017) Shoulder arthritis secondary to rotator cuff tear: A reproducible murine model and histopathologic scoring system. J Orthop Res 35:506-514
Li, Xing; Sun, Wen; Li, Jinbo et al. (2017) Clomipramine causes osteoporosis by promoting osteoclastogenesis via E3 ligase Itch, which is prevented by Zoledronic acid. Sci Rep 7:41358
Schwarz, Edward M (2017) Confirmation of Sexual Dimorphisms in Metal Hypersensitivity and Joint Pain Following Total Joint Arthroplasty: Commentary on an article by Marco S. Caicedo, PhD, et al.: ""Females with Unexplained Joint Pain Following Total Joint Arthroplasty Exhibit a H J Bone Joint Surg Am 99:e41
Zhang, Longze; Wang, Tao; Chang, Martin et al. (2017) Teriparatide Treatment Improves Bone Defect Healing Via Anabolic Effects on New Bone Formation and Non-Anabolic Effects on Inhibition of Mast Cells in a Murine Cranial Window Model. J Bone Miner Res 32:1870-1883
Feigenson, Marina; Eliseev, Roman A; Jonason, Jennifer H et al. (2017) PGE2 Receptor Subtype 1 (EP1) Regulates Mesenchymal Stromal Cell Osteogenic Differentiation by Modulating Cellular Energy Metabolism. J Cell Biochem 118:4383-4393
Wang, Wensheng; Wang, Hua; Zhou, Xichao et al. (2017) Lymphatic Endothelial Cells Produce M-CSF, Causing Massive Bone Loss in Mice. J Bone Miner Res 32:939-950
Sun, Wen; Zhang, Hengwei; Wang, Hua et al. (2017) Targeting Notch-Activated M1 Macrophages Attenuates Joint Tissue Damage in a Mouse Model of Inflammatory Arthritis. J Bone Miner Res 32:1469-1480

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