Literature DB >> 1729278

An anticoagulant dermatan sulfate proteoglycan circulates in the pregnant woman and her fetus.

M Andrew1, L Mitchell, L Berry, B Paes, M Delorme, F Ofosu, R Burrows, B Khambalia.   

Abstract

Investigation of the in vitro ability of plasma from pregnant women to inhibit exogenous thrombin (25 nM) demonstrated that heparin cofactor II inhibited more thrombin (3.0 +/- 0.7 nM, mean +/- SD) than plasma from women 3-5 d postpartum (1.9 +/- 0.5 nM) or plasma from nonpregnant adults (1.5 +/- 0.4 nM). Levels of heparin cofactor II were only slightly increased over normal in both pregnant and postpartum women and did not account for the observed increase in thrombin bound to heparin cofactor II. Assay of pregnancy plasma for dermatan sulfate anticoagulant activity demonstrated the presence of activity equivalent to 0.23 +/- 0.02 micrograms/ml of porcine mucosal dermatan sulfate. This activity could not be demonstrated in normal adult plasma or plasma from women on the contraceptive pill. The mass of dermatan sulfate in pregnancy and umbilical cord plasmas was increased over adult control plasma by 0.20 micrograms/ml (53%) and 0.29 micrograms/ml (76%), respectively. The glycosaminoglycan-containing fraction of plasma was isolated and an assay for anticoagulant dermatan sulfate confirmed its presence in both pregnancy and cord plasmas but minimal activity in adult plasma. Gel chromatography of isolated fractions from both pregnancy and cord plasmas revealed a polydisperse, active species with apparent Mr 150,000 D. Reductive elimination decreased the apparent Mr of the active species on gel chromatography to 31,000 D for cord and 21,000 D for pregnancy products. This confirmed the presence of an anticoagulant active dermatan sulfate proteoglycan circulating in the plasmas of pregnant women at term and fetuses at delivery.

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Year:  1992        PMID: 1729278      PMCID: PMC442851          DOI: 10.1172/JCI115579

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  46 in total

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2.  Functional and immunologic protein S levels are decreased during pregnancy.

Authors:  P C Comp; G R Thurnau; J Welsh; C T Esmon
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3.  Structure and expression of cDNA for an inhibitor of blood coagulation isolated from human placenta: a new lipocortin-like protein.

Authors:  A Iwasaki; M Suda; H Nakao; T Nagoya; Y Saino; K Arai; T Mizoguchi; F Sato; H Yoshizaki; M Hirata
Journal:  J Biochem       Date:  1987-11       Impact factor: 3.387

4.  Inhibition of human factor VIIa-tissue factor activity by placental anticoagulant protein.

Authors:  S Kondo; M Noguchi; T Funakoshi; K Fujikawa; W Kisiel
Journal:  Thromb Res       Date:  1987-11-15       Impact factor: 3.944

5.  Catalysis of thrombin inhibition provides an index for estimating the antithrombotic potential of glycosaminoglycans in rabbits.

Authors:  F A Fernandez; M R Buchanan; J Hirsh; J W Fenton; F A Ofosu
Journal:  Thromb Haemost       Date:  1987-06-03       Impact factor: 5.249

6.  Fibrinolysis during normal human pregnancy: complex inter-relationships between plasma levels of tissue plasminogen activator and inhibitors and the euglobulin clot lysis time.

Authors:  J G Wright; P Cooper; B Astedt; I Lecander; J T Wilde; F E Preston; M Greaves
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7.  Extraction and analysis of glycosaminoglycans from intima-media of single rabbit aortae: effect of balloon catheter de-endothelialization on the content and profile of glycosaminoglycans.

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8.  Increased thrombin generation in normal pregnancy.

Authors:  S Pinto; R Abbate; C Rostagno; V Bruni; D Rosati; G G Neri Serneri
Journal:  Acta Eur Fertil       Date:  1988 Sep-Oct

9.  Fibrinolysis in pregnancy: a study of plasminogen activator inhibitors.

Authors:  E K Kruithof; C Tran-Thang; A Gudinchet; J Hauert; G Nicoloso; C Genton; H Welti; F Bachmann
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Authors:  B Schmidt; L Mitchell; F A Ofosu; M Andrew
Journal:  Thromb Haemost       Date:  1989-12-29       Impact factor: 5.249

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Journal:  Blood       Date:  2005-12-08       Impact factor: 22.113

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5.  Alterations of fibrin network structure mediated by dermatan sulfate.

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