Imamura et al. (1990) |
Osteoblast-like MC3T3-E1 cells |
0.5–2 atm |
Static |
Inhibition of osteoblast differentiation, promotion of osteoclast production (“optimum” pressure: 100 kPa), increased PGE synthesis |
Ozawa et al. (1990) |
Mouse osteoblast-like MC3T3-E1 cell |
1 and 3 atm |
Continuous |
Decreased osteoblast numbers, increased PGE2 expression |
Klein-Nulend et al. (1995) |
Osteocytes from chicken calvariae |
13 kPa |
0.3 Hz (1 s loading, 2 s relaxation), for 24 h |
Increase in prostaglandin release (can enhance bone formation) |
Roelofsen et al. (1995) |
Neonatal mouse calvarial cells |
13 kPa |
0.3 Hz |
Stimulation of osteoblastic activity, stimulation of actin expression, AP activity |
Brighton et al. (1996) |
Calvarial bone cells from neonatal rats, exhibiting an osteoblast phenotype |
17.2–69 kPa |
1 Hz, for 10 cycles |
increased proliferation, increased cytosolic calcium concentration |
Vergne et al. (1996) |
ROS 17/2.8 (rat osteoblast-like cells) |
50–90 kPa |
1 and 0.1 Hz, 20 min test duration |
Increase in cell saturation density (for a frequency of 1 Hz), decreases alkaline phosphatase activity |
Rubin et al. (1997) |
Marrow cells from tibiae and femurs of C57BL/6 mice |
1–2 atm |
Static |
Decreased osteoclast formation, decrease in mRNA coding for the membrane-bound form of MCSF |
Nagatomi et al. (2001) |
Osteoblasts from the calvaria of neonatal rats |
10–40 kPa |
0.25 or 1 Hz, 1 h daily |
Elongated pressure decreases osteoblast proliferation, the same pressure stimulus causes different effect on different cells |
Nagatomi et al. (2002) |
Bone marrow cells (source of osteoclasts) from rat femurs |
10–40 kPa |
1 Hz (sinusoidal wave form), for 1 h per day |
Reduced osteoclast differentiation and resorption activity, lower concentration of IL-1, down-regulation of mRNA expression for IL-1, IL-1, and TNF-
|
Nagatomi et al. (2003) |
Osteoblasts isolated from rat calvariae |
10–40 kPa |
1 Hz, for 1 h daily |
Increased type-I collagen mRNA expression, increased amount of acid-soluble collagen, increased calcium concentration |
Takai et al. (2004) |
Primary osteoblasts obtained from trabecular bone cores taken from the epiphyses of metacarpal bones from 3- to 4-month-old calves |
3 MPa |
0.33 Hz (triangle wave form), for 1 h/day |
Increased osteoblast function (only when osteocytes are present), increased osteocyte viability |
Maul et al. (2007) |
Bone marrow progenitor cells from rats |
10–16 kPa |
1 Hz |
Enhanced proliferation |
Gardinier et al. (2009) |
MC3T3 osteoblast-like cells |
0–68 kPa |
0.5 Hz |
Increased anabolic response, increase in ATP release, increased COX-2 levels |
Liu et al. (2009) |
Bone marrow stromal cells from tibiae and femurs of rats |
10–36 kPa |
0.25 Hz (sinusoidal wave form) |
Increase in osteoblast activity-related transcription factors |
Liu et al. (2010) |
MLO-Y4 osteocyte-like cells (i.e., deriving from cells extracted from transgenic mice) |
68 kPa |
0.5 Hz (triangular wave form), for 1 or 2 h |
Decreased osteocyte apoptosis, increase in intracellular calcium (after 40 s, may be related to osteoblast activity), of RANKL/OPG ratio (after 2 h), and of COX-2 mRNA level (after 1 h) |
Rottmar et al. (2011) |
Human bone- derived cells, from the hip marrow |
1–11 kPa |
30 min stimulation, 7 h, 30 min break |
Increased osteogenic differentiation and proliferation |
Henstock et al. (2013) |
Cells contained in whole femurs of chick foetuses |
0–279 kPa |
0.0001–2 Hz |
Increased volume of diaphysial collar |