? The broad, long-term objective of this project is to understand the barrier properties of a confluent osteoblastic monolayer, which will provide insight into the role of the osteoblastic lining cell system in the physiology and pathophysiology of bone. This layer of cells that covers all resting surfaces in bone is expected to serve a """"""""gatekeeper"""""""" role in the development of hydraulic and electric resistance as well as passage of material, e.g., water, nutrients, ions, waste products and growth factors, into and out of bone tissue. It is this gatekeeper role that lends bone the ability to function as an organ within vertebrate systems.
The Specific Aims of this project are (1) to study the permeability characteristics of water as well as specific nutrients (glucose), ions (calcium and phosphate) and growth factors (insulin, PTH) in a static environment, allowing for simple diffusion and pressure head differences between the apical and basal surfaces as well as (2) in dynamic environments exposed to cyclic flow regimes on the apical and basal surfaces of the membrane. For each of these aims, the effect of PTH on barrier function will be studied in situ. The research design is to measure baseline values for hydraulic and electrical conductivity as well as concentration gradients of water, nutrient (glucose), ion (Ca and P) and growth factor transport (insulin, and PTH or a fluorescent tagged, inert analog such as dextran) due to diffusion and static pressure across the osteoblast cell membrane. A confluent monolayer of osteoblasts from the paraosteosarcoma cell line UMR-106-01-BSP will be used as a model system. To address the first aim, pressure will be provided through a pressure head on either side of the membrane in an Ussing chamber. To address the second aim, an innovative dual flow chamber system will be built, tested and implemented as a physiological cell culture model. In both cases, electrical resistance and hydraulic conductance will be measured across the membrane, and glucose, calcium, phosphate, PTH and insulin will be measured in the apical and basal media. The proposed project represents an innovative departure from conventional understanding of bone physiology. This study is expected to provide insight into new strategies for treatment of bone diseases such as osteoporosis and osteoarthritis. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AR049351-02
Application #
6662547
Study Section
Special Emphasis Panel (ZAR1-RJB-A (O1))
Program Officer
Sharrock, William J
Project Start
2002-09-23
Project End
2005-05-31
Budget Start
2003-06-01
Budget End
2005-05-31
Support Year
2
Fiscal Year
2003
Total Cost
$73,760
Indirect Cost
Name
Cleveland Clinic Lerner
Department
Type
DUNS #
017730458
City
Cleveland
State
OH
Country
United States
Zip Code
44195
Anderson, Eric J; Knothe Tate, Melissa L (2007) Design of tissue engineering scaffolds as delivery devices for mechanical and mechanically modulated signals. Tissue Eng 13:2525-38
Anderson, Eric J; Kaliyamoorthy, Sathya; Iwan, J et al. (2005) Nano-microscale models of periosteocytic flow show differences in stresses imparted to cell body and processes. Ann Biomed Eng 33:52-62
Knothe Tate, Melissa L; Adamson, Josee R; Tami, Andrea E et al. (2004) The osteocyte. Int J Biochem Cell Biol 36:1-8
Sorkin, Adam M; Dee, Kay C; Knothe Tate, Melissa L (2004) ""Culture shock"" from the bone cell's perspective: emulating physiological conditions for mechanobiological investigations. Am J Physiol Cell Physiol 287:C1527-36