Bone cells occupy fluid filled lacunae in the mineralized matrix and are interconnected by canaliculi. As bone is cyclically loaded, fluid flows in the lacunar-canalicular network from regions of high matrix strain to low matrix strain and back in an oscillatory fashion. Although it has been demonstrated that bone cells respond to steady and pulsatile fluid flow with a transient elevation in intracellular calcium concentration, increased release of paracrine factors, and increased gene transcription, our preliminary data indicate that these responses may be fundamentally different from those observed for oscillating flow. To date no experimental system has been designed to study responsiveness to physiologic oscillating fluid flow as a function of frequency and flow rate. To this end, the Principal Investigator and his co-investigators have developed a functioning oscillatory fluid flow exposure apparatus. This has allowed them to observe a frequency dependent intracellular calcium response to physiologic levels of oscillating fluid flow. The central hypothesis is that physiologic levels of oscillatory fluid flow provide an important mechanism of mechanotransduction, and furthermore shear stress level, frequency, time course, low level steady flow and cell dimensions modulate the cellular response. To test this hypothesis the investigators will apply combinations of shear stress, altering level and frequency, and measure cell signaling and metabolism. They are also interested in whether the intracellular calcium response to oscillating flow is followed by a refractory period as well as the possibility that oscillating and low level steady fluid are together synergistic. Finally studies are proposed to investigate the influence of cell dimension on response. The long-term goal is to understand how mechanical loading influences the behavior of bone.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
7R01AR045989-02
Application #
6413160
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Program Officer
Sharrock, William J
Project Start
2000-07-15
Project End
2004-06-30
Budget Start
2001-01-15
Budget End
2001-06-30
Support Year
2
Fiscal Year
2000
Total Cost
$117,876
Indirect Cost
Name
Stanford University
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Downs, Matthew E; Nguyen, An M; Herzog, Florian A et al. (2014) An experimental and computational analysis of primary cilia deflection under fluid flow. Comput Methods Biomech Biomed Engin 17:2-10
Leucht, P; Monica, S D; Temiyasathit, S et al. (2013) Primary cilia act as mechanosensors during bone healing around an implant. Med Eng Phys 35:392-402
Nguyen, An M; Jacobs, Christopher R (2013) Emerging role of primary cilia as mechanosensors in osteocytes. Bone 54:196-204
Chen, Julia C; Jacobs, Christopher R (2013) Mechanically induced osteogenic lineage commitment of stem cells. Stem Cell Res Ther 4:107
Hoey, David A; Tormey, Shane; Ramcharan, Stacy et al. (2012) Primary cilia-mediated mechanotransduction in human mesenchymal stem cells. Stem Cells 30:2561-70
Castillo, Alesha B; Blundo, Jennifer T; Chen, Julia C et al. (2012) Focal adhesion kinase plays a role in osteoblast mechanotransduction in vitro but does not affect load-induced bone formation in vivo. PLoS One 7:e43291
Young, Y-N; Downs, M; Jacobs, C R (2012) Dynamics of the primary cilium in shear flow. Biophys J 103:629-39
Hoey, David A; Downs, Matthew E; Jacobs, Christopher R (2012) The mechanics of the primary cilium: an intricate structure with complex function. J Biomech 45:17-26
Case, N; Sen, B; Thomas, J A et al. (2011) Steady and oscillatory fluid flows produce a similar osteogenic phenotype. Calcif Tissue Int 88:189-97
Hoey, David A; Kelly, Daniel J; Jacobs, Christopher R (2011) A role for the primary cilium in paracrine signaling between mechanically stimulated osteocytes and mesenchymal stem cells. Biochem Biophys Res Commun 412:182-7

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