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Differential regulation of mesothelial cell fibrinolysis by transforming growth factor beta 1.

Falk, Peter, 1962 (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna,Institute of Surgical Sciences
Ma, C (author)
Chegini, N (author)
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Holmdahl, Lena, 1954 (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för kirurgi,Institute of Surgical Sciences, Department of Surgery
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 (creator_code:org_t)
2000
2000
English.
In: Scandinavian journal of clinical and laboratory investigation. - 0036-5513. ; 60:6, s. 439-47
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Inflammation and tissue trauma during the surgical procedure reduce the peritoneal fibrinolytic capacity. These conditions promote adhesion formation, and are associated with increased expression of transforming growth factor beta 1 (TGF-beta1). The objective of the present study was to investigate whether TGF-beta1 regulates the expression of fibrinolytic components in peritoneal mesothelial cells. Human peritoneal mesothelial cells (HPMC) were cultured and treated with various concentrations of human recombinant TGF-beta1 (0.1, 1.0 and 10 ng/mL) for 24 h. Levels of tissue- and urokinase plasminogen activator (t-PA and uPA), plasminogen activator inhibitor type-1 (PAI-1) and type-2 (PAI-2) mRNA and protein were assessed by quantitative reverse transcriptase polymerase chain reaction (Q-RT-PCR) and ELISA, respectively. HPMC expressed these components at the gene and protein level. TGF-beta1 downregulated, dose-dependently t-PA mRNA and protein to about 50% of control values (p = 0.0010), and doubled PAI-1 protein production (p = 0.0008) compared to untreated controls. Although uPA gene expression increased in cells exposed to TGF-beta1, the corresponding protein concentration in conditioned media did not. PAI-2 was not affected, either at the gene or protein level. In conclusion, the results indicate that fibrinolytic capacity of mesothelial cells is reduced by TGF-beta1, suggesting that peritoneal adhesion formation induced by TGF-beta1 may be mediated, in part, through reduction in fibrin degradation capacity at an early stage of peritoneal tissue repair.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

Enzyme-Linked Immunosorbent Assay
Epithelial Cells
drug effects
Fibrinolysis
genetics
Gene Expression Profiling
Humans
Peritoneal Cavity
pathology
physiopathology
Plasminogen Activator Inhibitor 1
genetics
Plasminogen Activator Inhibitor 2
genetics
RNA
Messenger
genetics
metabolism
Receptors
Cell Surface
genetics
Receptors
Urokinase Plasminogen Activator
Recombinant Proteins
pharmacology
Reverse Transcriptase Polymerase Chain Reaction
Tissue Plasminogen Activator
genetics
Transforming Growth Factor beta
pharmacology
Urokinase-Type Plasminogen Activator
genetics

Publication and Content Type

ref (subject category)
art (subject category)

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Falk, Peter, 196 ...
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Chegini, N
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