TY - JOUR
T1 - Effect of oxidized regenerated cellulose (Interceed®) on the expression of tissue plasminogen activator and plasminogen activator inhibitor-1 in human peritoneal fibroblasts and mesothelial cells
AU - Gago, L. April
AU - Saed, Ghassan
AU - Elhammady, Eslam
AU - Diamond, Michael P.
N1 - Funding Information:
Supported by the Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, Michigan.
PY - 2006/10
Y1 - 2006/10
N2 - Objective: To characterize the molecular changes that occur in normal fibroblasts, adhesion fibroblasts, and mesothelial cells as a result of exposure to oxidized regenerated cellulose (Interceed®; Johnson & Johnson Medical, Inc., New Brunswick, NJ). Design: Control and Interceed®-treated normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells in culture were assessed for messenger RNA levels of molecules known to be associated with adhesion development, using multiplex reverse transcriptase polymerase chain reaction (n = 4). Setting: University research laboratory. Patient(s): Normal and adhesion fibroblasts and mesothelial cells. Intervention(s): Exposure of cells, normal fibroblasts, adhesion fibroblasts, and mesothelial cells to oxidized regenerated cellulose. Main Outcome Measure(s): Real-time reverse transcriptase polymerase chain reaction expression of messenger RNA tissue plasminogen activator (tPA), plasminogen activator inhibitor-1 (PAI-1), and tPA-PAI-1 ratio, an indicator of overall fibrinolytic activity. Result(s): Interceed® treatment of normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells results in an increased expression of tPA in mesothelial cells and an increase in the tPA-PAI-1 ratio, signifying an overall increase in fibrinolytic activity. Conclusion(s): Interceed®, which has been shown in multiple human in vivo studies to decrease postoperative adhesion development, increases the expression of tPA and the tPA-PAI-1 ratio (an indicator of overall fibrinolytic activity), thereby promoting dissolution of fibrin and healing without adhesion development. Thus, the ability of Interceed® to reduce postoperative adhesion development may be derived from both a barrier and biologic effect.
AB - Objective: To characterize the molecular changes that occur in normal fibroblasts, adhesion fibroblasts, and mesothelial cells as a result of exposure to oxidized regenerated cellulose (Interceed®; Johnson & Johnson Medical, Inc., New Brunswick, NJ). Design: Control and Interceed®-treated normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells in culture were assessed for messenger RNA levels of molecules known to be associated with adhesion development, using multiplex reverse transcriptase polymerase chain reaction (n = 4). Setting: University research laboratory. Patient(s): Normal and adhesion fibroblasts and mesothelial cells. Intervention(s): Exposure of cells, normal fibroblasts, adhesion fibroblasts, and mesothelial cells to oxidized regenerated cellulose. Main Outcome Measure(s): Real-time reverse transcriptase polymerase chain reaction expression of messenger RNA tissue plasminogen activator (tPA), plasminogen activator inhibitor-1 (PAI-1), and tPA-PAI-1 ratio, an indicator of overall fibrinolytic activity. Result(s): Interceed® treatment of normal peritoneal fibroblasts, adhesion fibroblasts, and mesothelial cells results in an increased expression of tPA in mesothelial cells and an increase in the tPA-PAI-1 ratio, signifying an overall increase in fibrinolytic activity. Conclusion(s): Interceed®, which has been shown in multiple human in vivo studies to decrease postoperative adhesion development, increases the expression of tPA and the tPA-PAI-1 ratio (an indicator of overall fibrinolytic activity), thereby promoting dissolution of fibrin and healing without adhesion development. Thus, the ability of Interceed® to reduce postoperative adhesion development may be derived from both a barrier and biologic effect.
KW - Adhesions
KW - Interceed®
KW - PAI-1
KW - adhesion barriers
KW - adhesion fibroblasts
KW - fibrinolysis
KW - mesothelial cells
KW - tPA
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U2 - 10.1016/j.fertnstert.2006.04.021
DO - 10.1016/j.fertnstert.2006.04.021
M3 - Article
C2 - 17008148
AN - SCOPUS:33748883853
SN - 0015-0282
VL - 86
SP - 1223
EP - 1227
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 4 SUPPL.
ER -