Although osteocytes make up over 90% of all bone cells, little is known about their function compared to other bone cells, the osteoblast and the osteoclast. The osteocyte is the cell ideally situated in bone to sense mechanical strain and translate that strain into signals for bone formation and bone resorption. However, the role of osteocytes in modulating strain effects on bone modeling and remodeling is unclear. This Program Project Grant was initiated to develop a team approach to determine the function of osteocytes and response to mechanical strain. The hypothesis to be tested is that osteocytes sense and respond to mechanical strain and in turn send signals that result in either bone loss, remodeling, modeling, or pathologic repair. The mechanisms whereby osteocytes translate mechanical strain into signals include intracellular and extracellular signaling and the expression of genes necessary and specific for osteocyte function.
The specific aims of the program project are: 1) To determine the levels of mechanical strain sensed by the osteocyte that result in change of bone mass, 2). To determine the role of E11 in the formation and function of osteocytic dendritic processes, 3) To determine the function and regulation of hemichannels in osteocytes, 4) To determine the function of Dmp1 in osteocytes, and 5). To correlate magntitude of strain with gene expression with biological response. Novel approaches to accomplish these specific aims include the use of an osteocyte-like cell line, primary osteocytes expressing a fluorescent reporter, the use of bioengineering techniques to measure strain sensed by individual osteocytes, transgenic technology, novel means of imaging the osteocyte lacuno-canalicular system, fluorescent image analysis to examine gene expression in single cells and targeted deletion of genes in osteocytes in vivo to examine genes regulated by mechanical strain. This program project is composed of investigators with specific talents, training and expertise in the areas of molecular biology, biochemistry, cell biology and bioengineering who together work in a multidisciplinary manner to integrate, improve, and expand approaches to examine osteocyte function and response to strain. Knowledge gained from the accomplishment of these specific aims will be applied to the prevention and treatment of bone loss due to immobilization, space flight, microdamage, and disease states such as osteoporosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR046798-09
Application #
7595762
Study Section
Special Emphasis Panel (ZAR1-YZW-J (O3))
Program Officer
Sharrock, William J
Project Start
2000-04-01
Project End
2011-03-31
Budget Start
2009-04-01
Budget End
2010-03-31
Support Year
9
Fiscal Year
2009
Total Cost
$1,263,309
Indirect Cost
Name
University of Missouri Kansas City
Department
Dentistry
Type
Schools of Dentistry
DUNS #
010989619
City
Kansas City
State
MO
Country
United States
Zip Code
64110
Kitase, Yukiko; Vallejo, Julian A; Gutheil, William et al. (2018) ?-aminoisobutyric Acid, l-BAIBA, Is a Muscle-Derived Osteocyte Survival Factor. Cell Rep 22:1531-1544
Jähn, Katharina; Kelkar, Shilpa; Zhao, Hong et al. (2017) Osteocytes Acidify Their Microenvironment in Response to PTHrP In Vitro and in Lactating Mice In Vivo. J Bone Miner Res 32:1761-1772
Zhao, Ning; Nociti Jr, Francisco H; Duan, Peipei et al. (2016) Isolation and Functional Analysis of an Immortalized Murine Cementocyte Cell Line, IDG-CM6. J Bone Miner Res 31:430-442
Duan, Peipei; Bonewald, L F (2016) The role of the wnt/?-catenin signaling pathway in formation and maintenance of bone and teeth. Int J Biochem Cell Biol 77:23-29
Yamamoto, Hiroyuki; Ramos-Molina, Bruno; Lick, Adam N et al. (2016) Posttranslational processing of FGF23 in osteocytes during the osteoblast to osteocyte transition. Bone 84:120-130
Prideaux, Matthew; Dallas, Sarah L; Zhao, Ning et al. (2015) Parathyroid Hormone Induces Bone Cell Motility and Loss of Mature Osteocyte Phenotype through L-Calcium Channel Dependent and Independent Mechanisms. PLoS One 10:e0125731
Riquelme, Manuel A; Burra, Sirisha; Kar, Rekha et al. (2015) Mitogen-activated Protein Kinase (MAPK) Activated by Prostaglandin E2 Phosphorylates Connexin 43 and Closes Osteocytic Hemichannels in Response to Continuous Flow Shear Stress. J Biol Chem 290:28321-8
Kamel-ElSayed, Suzan A; Tiede-Lewis, LeAnn M; Lu, Yongbo et al. (2015) Novel approaches for two and three dimensional multiplexed imaging of osteocytes. Bone 76:129-40
Xu, Huiyun; Gu, Sumin; Riquelme, Manuel A et al. (2015) Connexin 43 channels are essential for normal bone structure and osteocyte viability. J Bone Miner Res 30:436-48
Kitase, Y; Lee, S; Gluhak-Heinrich, J et al. (2014) CCL7 is a protective factor secreted by mechanically loaded osteocytes. J Dent Res 93:1108-15

Showing the most recent 10 out of 97 publications