Although standard techniques are available, intra-laboratory variation in the quality andnumber of bone cells available for research purposes at Yale has varied considerably. Toaddress this limitation and to advance productive scholarship, the Yale Core Center forMusculoskeletal Disorders developed the Cell Core. The mission of the Cell Core is tofacilitate the experimental use of authentic, primary, mouse and rat osteoblastic cells as wellas osteoclasts generated from in vitro culture.As part of our new initiatives bone marrow derived mesenchymal stem cells (MSCs) are nowavailable to Core investigators. Although outside the original mandate of the Core, theDirector has made his PIXImus machine available to Center members through an agreementwith the Densitometry subunit of the Physiology Core.
The Specific Aims of the current proposal are to provide the following services:1. Isolate and cultivate primary murine and fetal rat calvarial osteoblasts. This will includelarge-scale preparations for biochemical studies and RNA and DNA purification.2. Cultivate murine osteoclast-like cells generated from: 1) in vitro co-culture 2) culture with MCSFand RANKL.3. Maintain a wide range of frozen cell lines.4. Provide small animal bone densitometry (DEXA).5. Cultivate mouse bone marrow derived mesenchymal stem cells (MSCs).6. Train for in vitro isolation and culture of osteoblasts, osteoclasts and stromal cells, so thatinvestigators, appropriately trained, can initiate and maintain these cells in their laboratories.These services are coordinated under the directorship of Dr. Mark Horowitz, who has hadextensive experience with cell culture in general and the isolation and culture of bone cellsspecifically. The Cell Core is particularly anxious to support current and future Pilot andFeasibility Projects as part of the Center's ongoing effort to attract new investigators tomusculoskeletal research.PERFORMANCE SITE(S) (organization, ci

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR046032-10
Application #
7609125
Study Section
Special Emphasis Panel (ZAR1)
Project Start
2008-04-01
Project End
2009-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
10
Fiscal Year
2008
Total Cost
$149,785
Indirect Cost
Name
Yale University
Department
Type
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Zhu, Meiling; Sun, Ben-Hua; Saar, Katarzyna et al. (2016) Deletion of Rac in Mature Osteoclasts Causes Osteopetrosis, an Age-Dependent Change in Osteoclast Number, and a Reduced Number of Osteoblasts In Vivo. J Bone Miner Res 31:864-73
Belinsky, Glenn S; Sreekumar, Bharath; Andrejecsk, Jillian W et al. (2016) Pigment epithelium-derived factor restoration increases bone mass and improves bone plasticity in a model of osteogenesis imperfecta type VI via Wnt3a blockade. FASEB J 30:2837-48
Meijome, Tomas E; Hooker, R Adam; Cheng, Ying-Hua et al. (2015) GATA-1 deficiency rescues trabecular but not cortical bone in OPG deficient mice. J Cell Physiol 230:783-90
Wang, Meina; Nasiri, Ali R; Broadus, Arthur E et al. (2015) Periosteal PTHrP Regulates Cortical Bone Remodeling During Fracture Healing. Bone 81:104-111
Kim, Jae Geun; Sun, Ben-Hua; Dietrich, Marcelo O et al. (2015) AgRP Neurons Regulate Bone Mass. Cell Rep 13:8-14
Protiva, Petr; Gong, Jingjing; Sreekumar, Bharath et al. (2015) Pigment Epithelium-Derived Factor (PEDF) Inhibits Wnt/?-catenin Signaling in the Liver. Cell Mol Gastroenterol Hepatol 1:535-549.e14
Ardeshirpour, Laleh; Dumitru, Cristina; Dann, Pamela et al. (2015) OPG Treatment Prevents Bone Loss During Lactation But Does Not Affect Milk Production or Maternal Calcium Metabolism. Endocrinology 156:2762-73
Yao, Chen; Yao, Gang-Qing; Sun, Ben-Hua et al. (2014) The transcription factor T-box 3 regulates colony-stimulating factor 1-dependent Jun dimerization protein 2 expression and plays an important role in osteoclastogenesis. J Biol Chem 289:6775-90
McCarthy, Thomas L; Yun, Zhong; Madri, Joseph A et al. (2014) Stratified control of IGF-I expression by hypoxia and stress hormones in osteoblasts. Gene 539:141-51
Wang, Meina; Nasiri, Ali; VanHouten, Joshua N et al. (2014) The remarkable migration of the medial collateral ligament. J Anat 224:490-8

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