References : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
Ehrlich PJ, Lanyon LE. Mechanical strain and bone cell function: a review. Osteoporos Int. 2002;13(9):688–700.
Vaughan TJ, Haugh MG, Mcnamara LM. A fluid-structure interaction model to characterize bone cell stimulation in parallel-plate flow chamber systems. J R Soc Interface. 2013;10(81):20120900.
Weinbaum S, Cowin SC, Zeng Y. A model for the excitation of osteocytes by mechanical loading-induced bone fluid shear stresses. J Biomech. 1994;27(3):339–60.
Anderson EJ, Falls TD, Sorkin AM, Knothe Tate ML. The imperative for controlled mechanical stresses in unraveling cellular mechanisms of mechanotransduction. Biomed Eng Online. 2006;5:27.
Bancroft GN, Sikavitsas VI, van den Dolder J, Sheffield TL, Ambrose CG, Jansen JA, et al. Fluid flow increases mineralized matrix deposition in 3D perfusion culture of marrow stromal osteoblasts in a dose-dependent manner. Proc Natl Acad Sci U S A. 2002;99(20):12600–5.
Datta N, Pham QP, Sharma U, Sikavitsas VI, Jansen JA, Mikos AG. In vitro generated extracellular matrix and fluid shear stress synergistically enhance 3D osteoblastic differentiation. Proc Natl Acad Sci U S A. 2006;103(8):2488–93.
Yu X, Botchwey EA, Levine EM, Pollack SR, Laurencin CT. Bioreactor-based bone tissue engineering: the influence of dynamic flow on osteoblast phenotypic expression and matrix mineralization. Proc Natl Acad Sci U S A. 2004;101(31):11203–8.
Pavalko FM, Chen NX, Turner CH, Burr DB, Atkinson S, Hsieh YF, et al. Fluid shear-induced mechanical signaling in MC3T3-E1 osteoblasts requires cytoskeleton-integrin interactions. Am J Physiol. 1998;275(6 Pt 1):C1591–601.
Astrof NS, Salas A, Shimaoka M, Chen J, Springer TA. Importance of force linkage in mechanochemistry of adhesion receptors. Biochemistry. 2006;45(50):15020–8.
Bakker DP, van der Plaats A, Verkerke GJ, Busscher HJ, van der Mei HC. Comparison of velocity profiles for different flow chamber designs used in studies of microbial adhesion to surfaces. Appl Environ Microbiol. 2003;69(10):6280–7.
Bannister SR, Lohmann CH, Liu Y, Sylvia VL, Cochran DL, Dean DD, et al. Shear force modulates osteoblast response to surface roughness. J Biomed Mater Res. 2002;60(1):167–74.
Serial posts:
- Abstract : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Background : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- Background : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- Methods : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- Methods : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- Results : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- Results : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- Discussion : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- Discussion : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- Discussion : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [3]
- Conclusions : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Abbreviations : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- References : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- References : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- References : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [3]
- References : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [4]
- Acknowledgements : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Author information : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [1]
- Author information : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up [2]
- Rights and permissions : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- About this article : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Table 1 Listing of the single components of the flow chamber together with manufacturers’ data : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Table 2 Listing of the culture media and additives together with manufacturers’ data : Cellular fluid shear stress on implant surfaces—establishment of a novel experimental set up
- Fig. 1. Three-dimensional illustration (a–e) and photography (f) of the experimental setup with the components marked numerical. a1 Lower petri dish (s’ bottom serving as the lower plate); 2 Rotating glass panel [60 mm diameter (cell bearing)]; 3 Titanium axis. b4 Liquid medium (red). c5 Reversed upper petri dish. d6 Gearwheel with set screw. e7 Closing; 8 Electronic motor device and adjusting ring with additional set screw : Cellular fluid shear stress on implant
- Fig. 2. Side view of a computerized simulation, showing the flow chambers’ lower compartment and the flow profile in between the two plates; shearing gap and bottom plate are shown on the left side; rotation speed = 200 rpm; colour code bar (left edge) showing shear force values [Pa] [1 Pa = 10 dyn/cm2]; flow direction presented by arrows : Cellular fluid shear stress on implant
- Fig. 3. Diagram for visualisation of the calculation of shear stress rates taking into account the centrifugal force and the glass plates’ dimensions. For example, at a distance of 25 mm from the centre of the upper plate, the shear forces’ value is 8.33 dyn/cm2, together with an additional centrifugal force that has a value of 0.55 dyn/cm2 : Cellular fluid shear stress on implant
- Fig. 4. Randomly orientated osteoblasts without influence of rotation (phallacidin fluorescence staining). On the left side with 200× and on the right side with 400× magnification. The white X on the coloured circle marks the location upon the plate where the osteoblasts were located. The red X marks the centre of the plate : Cellular fluid shear stress on implant
- Fig. 5. Osteoblasts with an orientation tendency after 24 h of rotation (phallacidin fluorescence staining). On the left side with 200× and on the right side with 400× magnification. The yellow arrows show the orientation of the cells. The red arched arrow within the coloured circle shows the direction of rotation. The dashed white line oriented to the right stands for the resulting centrifugal force. The dashed white line pointing upwards shows the direction of the resulting flow resistance. The solid white arrow stands for the vectorial sum of the abovementioned forces : Cellular fluid shear stress on implant