TY - JOUR
T1 - Separating fluid shear stress from acceleration during vibrations In Vitro
T2 - Identification of mechanical signals modulating the cellular response
AU - Uzer, Gunes
AU - Manske, Sarah L.
AU - Chan, M. Ete
AU - Chiang, Fu Pen
AU - Rubin, Clinton T.
AU - Frame, Mary D.
AU - Judex, Stefan
PY - 2012/9
Y1 - 2012/9
N2 - The identification of the physical mechanism(s) by which cells can sense vibrations requires the determination of the cellular mechanical environment. Here, we quantified vibration-induced fluid shear stresses in vitro and tested whether this system allows for the separation of two mechanical parameters previously proposed to drive the cellular response to vibration - fluid shear and peak accelerations. When peak accelerations of the oscillatory horizontal motions were set at 1 g and 60 Hz, peak fluid shear stresses acting on the cell layer reached 0.5 Pa. A 3.5-fold increase in fluid viscosity increased peak fluid shear stresses 2.6-fold while doubling fluid volume in the well caused a 2-fold decrease in fluid shear. Fluid shear was positively related to peak acceleration magnitude and inversely related to vibration frequency. These data demonstrated that peak shear stress can be effectively separated from peak acceleration by controlling specific levels of vibration frequency, acceleration, and/or fluid viscosity. As an example for exploiting these relations, we tested the relevance of shear stress in promoting COX-2 expression in osteoblast like cells. Across different vibration frequencies and fluid viscosities, neither the level of generated fluid shear nor the frequency of the signal were able to consistently account for differences in the relative increase in COX-2 expression between groups, emphasizing that other variables including out-of-phase accelerations of the nucleus may play a role in the cellular response to vibrations.
AB - The identification of the physical mechanism(s) by which cells can sense vibrations requires the determination of the cellular mechanical environment. Here, we quantified vibration-induced fluid shear stresses in vitro and tested whether this system allows for the separation of two mechanical parameters previously proposed to drive the cellular response to vibration - fluid shear and peak accelerations. When peak accelerations of the oscillatory horizontal motions were set at 1 g and 60 Hz, peak fluid shear stresses acting on the cell layer reached 0.5 Pa. A 3.5-fold increase in fluid viscosity increased peak fluid shear stresses 2.6-fold while doubling fluid volume in the well caused a 2-fold decrease in fluid shear. Fluid shear was positively related to peak acceleration magnitude and inversely related to vibration frequency. These data demonstrated that peak shear stress can be effectively separated from peak acceleration by controlling specific levels of vibration frequency, acceleration, and/or fluid viscosity. As an example for exploiting these relations, we tested the relevance of shear stress in promoting COX-2 expression in osteoblast like cells. Across different vibration frequencies and fluid viscosities, neither the level of generated fluid shear nor the frequency of the signal were able to consistently account for differences in the relative increase in COX-2 expression between groups, emphasizing that other variables including out-of-phase accelerations of the nucleus may play a role in the cellular response to vibrations.
KW - Finite element modeling
KW - Mechanical stimulation
KW - Osteoblasts
KW - Particle image velocimetry
KW - Shear stress
KW - Speckle photometry
UR - http://www.scopus.com/inward/record.url?scp=84866356010&partnerID=8YFLogxK
U2 - 10.1007/s12195-012-0231-1
DO - 10.1007/s12195-012-0231-1
M3 - Article
AN - SCOPUS:84866356010
SN - 1865-5025
VL - 5
SP - 266
EP - 276
JO - Cellular and Molecular Bioengineering
JF - Cellular and Molecular Bioengineering
IS - 3
ER -