TY - JOUR
T1 - Hydrostatic pressure modulates mRNA expressions for matrix proteins in human meniscal cells
AU - Suzuki, Toru
AU - Toyoda, Takashi
AU - Suzuki, Hiroshi
AU - Hisamori, Noriyuki
AU - Matsumoto, Hideo
AU - Toyama, Yoshiaki
PY - 2006/10/23
Y1 - 2006/10/23
N2 - There have been few reports describing the effects of mechanical loading on the metabolism of meniscal cells. The aim of this study was to investigate the effects of hydrostatic pressure on meniscal cell metabolism. Human meniscal cells were cultured in alginate beads for 3 days. They were then subjected to 4 MPa hydrostatic pressure for 4 hours in either a static or cyclic (1 Hz) mode using a specially designed and constructed system. Immediately after the pressure application, the messenger RNA levels for aggrecan, type I collagen, matrix metalloproteinases (MMP) -1, -3, -9, -13 and tissue inhibitors of metalloproteinases (TIMP) -1 and -2 were measured. It was found that the application of static hydrostatic pressure caused a significant decrease in mRNA expression for MMP-1 and -13 (p < 0.05). In contrast, the application of cyclic hydrostatic pressure was associated with a significant increase in type I collagen (p < 0.01), TIMP-1 and -2 mRNA expression (p < 0.01). These results would suggest that hydrostatic pressure in isolation can modulate mRNA expressions for matrix proteins in meniscal cells.
AB - There have been few reports describing the effects of mechanical loading on the metabolism of meniscal cells. The aim of this study was to investigate the effects of hydrostatic pressure on meniscal cell metabolism. Human meniscal cells were cultured in alginate beads for 3 days. They were then subjected to 4 MPa hydrostatic pressure for 4 hours in either a static or cyclic (1 Hz) mode using a specially designed and constructed system. Immediately after the pressure application, the messenger RNA levels for aggrecan, type I collagen, matrix metalloproteinases (MMP) -1, -3, -9, -13 and tissue inhibitors of metalloproteinases (TIMP) -1 and -2 were measured. It was found that the application of static hydrostatic pressure caused a significant decrease in mRNA expression for MMP-1 and -13 (p < 0.05). In contrast, the application of cyclic hydrostatic pressure was associated with a significant increase in type I collagen (p < 0.01), TIMP-1 and -2 mRNA expression (p < 0.01). These results would suggest that hydrostatic pressure in isolation can modulate mRNA expressions for matrix proteins in meniscal cells.
KW - Extracellular matrix
KW - Hydrostatic pressure
KW - Mechanical stress
KW - Meniscal cells
KW - mRNA expression
UR - http://www.scopus.com/inward/record.url?scp=33750064277&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33750064277&partnerID=8YFLogxK
M3 - Article
C2 - 17047280
AN - SCOPUS:33750064277
SN - 0006-355X
VL - 43
SP - 611
EP - 622
JO - Biorheology
JF - Biorheology
IS - 5
ER -