TY - JOUR
T1 - Molecular characterization of fibroblasts isolated from human peritoneum and adhesions
AU - Saed, Ghassan M.
AU - Zhang, Wendy
AU - Diamond, Michael P.
N1 - Funding Information:
Supported by the Scientific Research Fund of the Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, Michigan.
PY - 2001
Y1 - 2001
N2 - Objective: To determine the response of adhesion and peritoneal fibroblasts to hypoxia. Design: Prospective experimental study. Setting: University medical center. Patient(s): Primary cultures of fibroblasts established from the peritoneal and adhesion tissues of the same patients (n = 2) to minimize genetic variations.Intervention(s): Hypoxia treatment of the primary cultured fibroblast. Main Outcome Measure(s): Analyze the expression of extracellular matrix (ECM) components, metalloproteinases and their tissue inhibitors, growth factors, and cytokines in adhesion and peritoneal fibroblasts under normal and hypoxic conditions by reverse transcriptase/polymerase chain reaction analysis. Result(s): Compared to peritoneal fibroblasts, adhesion fibroblasts had a significant increase in the basal mRNA levels for collagen I, fibronectin, MMP-1, TIMP-1, TGF-β1, TGF-β2, and IL-10. Hypoxia resulted in a further increase in collagen 1, fibronectin, TIMP-1, TGF-β1, TGF-β2, IL-10, and IFN-γ mRNA levels in both peritoneal and adhesion fibroblasts. The increase was more profound in adhesion fibroblasts. Conclusion(s): Hypoxia induces molecular changes in both peritoneal and adhesion fibroblasts, creating a milieu that favors adhesion development. The effect of hypoxia was more profound on adhesion fibroblasts.
AB - Objective: To determine the response of adhesion and peritoneal fibroblasts to hypoxia. Design: Prospective experimental study. Setting: University medical center. Patient(s): Primary cultures of fibroblasts established from the peritoneal and adhesion tissues of the same patients (n = 2) to minimize genetic variations.Intervention(s): Hypoxia treatment of the primary cultured fibroblast. Main Outcome Measure(s): Analyze the expression of extracellular matrix (ECM) components, metalloproteinases and their tissue inhibitors, growth factors, and cytokines in adhesion and peritoneal fibroblasts under normal and hypoxic conditions by reverse transcriptase/polymerase chain reaction analysis. Result(s): Compared to peritoneal fibroblasts, adhesion fibroblasts had a significant increase in the basal mRNA levels for collagen I, fibronectin, MMP-1, TIMP-1, TGF-β1, TGF-β2, and IL-10. Hypoxia resulted in a further increase in collagen 1, fibronectin, TIMP-1, TGF-β1, TGF-β2, IL-10, and IFN-γ mRNA levels in both peritoneal and adhesion fibroblasts. The increase was more profound in adhesion fibroblasts. Conclusion(s): Hypoxia induces molecular changes in both peritoneal and adhesion fibroblasts, creating a milieu that favors adhesion development. The effect of hypoxia was more profound on adhesion fibroblasts.
KW - Adhesion
KW - Fibroblasts
KW - Hypoxia
KW - Peritoneum
KW - RT/PCR
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U2 - 10.1016/S0015-0282(00)01799-4
DO - 10.1016/S0015-0282(00)01799-4
M3 - Article
C2 - 11287032
AN - SCOPUS:0035064828
SN - 0015-0282
VL - 75
SP - 763
EP - 768
JO - Fertility and sterility
JF - Fertility and sterility
IS - 4
ER -