Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Elsevier BV ; 2014
    In:  Biochimica et Biophysica Acta (BBA) - General Subjects Vol. 1840, No. 3 ( 2014-03), p. 1188-1193
    In: Biochimica et Biophysica Acta (BBA) - General Subjects, Elsevier BV, Vol. 1840, No. 3 ( 2014-03), p. 1188-1193
    Type of Medium: Online Resource
    ISSN: 0304-4165
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2014
    detail.hit.zdb_id: 2209617-6
    SSG: 12
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    American Society of Hematology ; 2004
    In:  Blood Vol. 104, No. 11 ( 2004-11-16), p. 1936-1936
    In: Blood, American Society of Hematology, Vol. 104, No. 11 ( 2004-11-16), p. 1936-1936
    Abstract: Tissue factor (TF) is an integral membrane protein, which is the key initiator of blood coagulation in vivo. Due to the limited availability of natural TF, recombinant proteins of various lengths and origins have been extensively used in research and clinical laboratories worldwide. Experimental results acquired with recombinant TF proteins are frequently used for the understanding of the coagulation processes occurring in vivo, although there is a lack of data confirming the structural and functional identity of natural TF proteins from various sources and recombinant ones. In the current study, human TF from cultured monocytes and purified from placenta were compared with three different species of recombinant TF: 1–218 (extracellular domain only), 1–242 (lacking cytoplasmic domain) and 1–263 (full-length). Anti-TF mAbs gave 93–98% inhibition of TF activity for all TF species tested, in both natural and relipidated preparations. It was established that purified placental TF has a higher affinity for factor VIIa (Kd 0.13 nM) than recombinant counterparts 1–242 and 1–263 (Kd 0.50–0.80 nM). Similarly, placental TF is more efficient in factor X activation by the extrinsic Xase than recombinant TF 1–242 (the second order rate constants are 3.0x107 and 0.7x107 M−1s−1, respectively). We explored the use of these TF species as well as monocyte TF (purified/relipidated and present on LPS-stimulated monocytes) for the initiation of thrombin generation in two in vitro models of blood coagulation. At equimolar concentrations (5 pM; determined by immunoassay), when evaluated in synthetic plasma reconstituted with 2x108/ml platelets, recombinant TF 1-263 provided an initiation phase of ~4 min. Placental TF and relipidated monocyte TF had similar profiles of thrombin generation with an initiation phase of ~3 min. In contrast, 0.5 pM TF on LPS-stimulated monocytes gave an initiation phase of ~1 min. Even at 0.05 pM concentration, monocyte TF was as active as any relipidated protein at 5.0 pM. A similar pattern of relative TF activity was observed in whole blood and plasma PT clotting assays. TF on stimulated monocytes gave the highest activity, exceeding that of any relipidated protein by 100–200-fold. Recombinant TF 1–242 was more active than recombinant TF 1–263 and placental TF in the PT assay but less active in synthetic plasma and whole blood. The lowest overall activity was observed for relipidated monocyte TF. Our data suggest that TF proteins from different sources are different with respect to their functional properties.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2004
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    American Society of Hematology ; 2004
    In:  Blood Vol. 104, No. 11 ( 2004-11-16), p. 4012-4012
    In: Blood, American Society of Hematology, Vol. 104, No. 11 ( 2004-11-16), p. 4012-4012
    Abstract: Several factor VIII products, recombinant and natural, have been used for hemophilia A treatment worldwide. Typically, two activity-based assays (factor Xase and aPTT) are used for the assessment of factor VIII concentration in these products. Frequently, the results are dependent upon the assay and its modifications in different laboratories. In this study, we evaluated five pharmacologic factor VIII products (three lots of each) in three activity-based assays and in two immunoassays for the concentration and activity of factor VIII protein. Two factor VIII products were plasma-derived (Immunate and Hemofil M) and three were recombinant; two of these contained full-length factor VIII (Recombinate and Kogenate) and one was B-domainless (ReFacto). Albumin-free full-length recombinant factor VIII was used as a standard in all assays. In the factor Xase assay, all recombinant factor VIII products and Immunate at 1U/ml (indicated by manufacturer) showed activity similar to that of 0.7nM (1U/ml) standard, whereas activity of Hemofil M was 64–68% of the standard. In the aPTT assay both full-length recombinant products and Hemofil M displayed activity similar to the standard, whereas Immunate had increased (142% of standard) and ReFacto decreased (83% of standard) activity. In synthetic plasma, all three recombinant products had standard-like activity, whereas Hemofil M and Immunate were slightly more active than standard. The ELISA immunoassay revealed that the factor VIII protein content in Recombinate, Kogenate and Hemofil M corresponded to the units assigned by manufacturers (1.4–1.6x1012U/mol vs1.4x1012U/mol calculated for standard), whereas the specific activity of Immunate was 50% of that expected (0.7x1012U/mol). In contrast, the specific activity of ReFacto was almost 3-fold that of full-length factor VIII (4.0x1012U/mol). The data of this study indicate that: 1) factor VIII activity estimated in different assays gives dissimilar results; 2) the specific activity of factor VIII in various factor VIII products is different and, as a consequence, administration of an equal factor VIII activity in U/ml means the administration of different amounts of factor VIII protein.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2004
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Online Resource
    Online Resource
    American Society of Hematology ; 2008
    In:  Blood Vol. 112, No. 11 ( 2008-11-16), p. 1022-1022
    In: Blood, American Society of Hematology, Vol. 112, No. 11 ( 2008-11-16), p. 1022-1022
    Abstract: There are several hypotheses which attempt to explain changes in tissue factor (TF) activity on cell surfaces upon treatment with various agents (“encryption-de-encryption”). However, these hypotheses are mostly based upon conjectural data interpretation. We evaluated the influence of lipopolysaccharide (LPS) stimulation on the surface and total expression of TF antigen on/in THP-1 monocytic cells and the corresponding TF activity. A cell-based immunoassay was used for the quantitation of TF antigen on the surface of monocytic cells, coupled with contact pathway-inhibited (corn trypsin inhibitor; CTI) plasma and blood dilute PT, extrinsic factor (F)Xase and synthetic coagulation proteome assays. Prior to stimulation, the concentration of TF was 240±60 molecules/cell on the cell surface and 510±180 total molecules/cell in cell lysates (n=8). Upon stimulation with LPS (1μg/ml), the TF antigen concentration steadily increased reaching a maximum at 4 hr of stimulation (2400±360 molecules/cell on the cell surface and 8400±360 molecules/cell total). Coincidently, the intact cell FXa generation rate increased from 4.2 pM/s to 46.3 pM/s. The clotting time of multi-donor plasma decreased from 192s to 80s corresponding to a 35.7±4.9-fold increase in TF activity. Thus all assays are consistent with increased surface expression of TF. Kinetic studies showed that the KM of the complex enzyme (TF/FVIIa) formed on the surface of LPS-stimulated monocytes for FX is 0.73±0.07 μM and the kcat 59.4±1.8 s−1. The kinetic properties for the FXase formed in lysates of LPS-stimulated THP-1 cells are similar to those observed for the cell surface TF (see Table 1). However, when LPS-stimulated monocyte TF was purified to homogeneity and relipidated using synthetic phospholipid vesicles (PCPS), the efficiency for FX activation was significantly lower due to both an increased KM and decreased kcat. As a consequence, the second order rate constant for FX activation by the extrinsic FXase on the surface of PCPS was only 8±1% of that observed on stimulated intact cells or lysates. A comparison of purified and relipidated monocyte TF with that cell-bound in situ in the synthetic coagulation proteome with platelets at mean physiologic concentration (2x108/ml) showed that thrombin generation profiles were similar for the reactions initiated with 5 pM relipidated TF and 0.05 pM TF expressed on the cell surface; a difference in specific activity of approximately 100-fold. Similar results were observed in CTI-inhibited blood. CTI blood, triggered with 5 pM relipidated monocyte TF clotted in 310 s, whereas initiation with 1.2 pM monocyte TF in situ led to a 40 s clotting time with maximum rates of thrombin generation of 1.3 and & gt;7.0 nM/s, respectively. These data indicate that the increase in monocyte TF activity upon stimulation with LPS is related to an increased expression of TF protein on/in monocytic cells and that there are components of the cell membrane which substantially enhance TF activity and these accessories maintain their function(s) in cell lysates. These components are not represented by synthetic (PCPS) phospholipid vesicles. Our data emphasize the importance of cell membrane composition on TF activity and are in agreement with observations published by Pendurthi et al. (Blood2007;110:3900). Table 1. Monocytic TF in the extrinsic FXase Preparation of TF KM(μM) kcat(s−1) kcat/KM((μM•s−1) In situ 0.73±0.0 59.4±1.8 81.4 In lysates 0.41±0.0 44.6±0.1 108.8 On PCPS 1.54±0.14 12.0±0.4 7.8
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2008
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    Georg Thieme Verlag KG ; 2008
    In:  Thrombosis and Haemostasis Vol. 99, No. 01 ( 2008), p. 142-149
    In: Thrombosis and Haemostasis, Georg Thieme Verlag KG, Vol. 99, No. 01 ( 2008), p. 142-149
    Abstract: It has been established that inflammation and enhanced procoagulant activity are associated with the pathogenesis of atherosclerotic vascular disease. We evaluated and compared the contributions of the factor (F)XIa and tissue factor (TF) activity in plasma of patients with coronary artery disease (CAD). Citrate plasma was obtained prior to therapy from 53 patients with stable angina (29 with a history of previous myocardial infarction; CAD-MI) and 30 with acute coronary syndrome (ACS) within 12 hours from pain onset. Four ACS patients treated with heparin were excluded. FXIa andTF activity were determined in clotting assays based upon the prolongation of clotting time by inhibitory monoclonal antibodies. Twenty-five of 26ACS patients (96%) and 22 of 29 CAD-MI patients (76%) had quantifiable FXIa (50 ± 33 and 42 ± 45pM, respectively).Ten of 26 (38%) ACS patients and only three of 53 (6%) stable CAD patients showedTF activity ( 〈 0.4pM). No FXIa or TF activity was observed in agematched healthy controls (n=12).For both CAD-MI andACS patients, there were correlations (p 〈 0.05) between FXIa and interleukin-6 (R2= 0.59 and 0.39, respectively) and between FXIa and TAT (R2= 0.64 and 0.63, respectively). In conclusion, the majority of ACS and CAD-MI patients have circulating FXIa that correlates with markers of coagulation and inflammation.
    Type of Medium: Online Resource
    ISSN: 0340-6245 , 2567-689X
    Language: English
    Publisher: Georg Thieme Verlag KG
    Publication Date: 2008
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 2004
    In:  Journal of Biological Chemistry Vol. 279, No. 22 ( 2004-05), p. 22875-22882
    In: Journal of Biological Chemistry, Elsevier BV, Vol. 279, No. 22 ( 2004-05), p. 22875-22882
    Type of Medium: Online Resource
    ISSN: 0021-9258
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2004
    detail.hit.zdb_id: 2141744-1
    detail.hit.zdb_id: 1474604-9
    SSG: 12
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    In: The Journal of Bone and Joint Surgery-American Volume, Ovid Technologies (Wolters Kluwer Health), Vol. 97, No. 9 ( 2015-05), p. 751-757
    Type of Medium: Online Resource
    ISSN: 0021-9355
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2015
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    In: The Lancet, Elsevier BV, Vol. 389, No. 10078 ( 2017-04), p. 1519-1527
    Type of Medium: Online Resource
    ISSN: 0140-6736
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2017
    detail.hit.zdb_id: 2067452-1
    detail.hit.zdb_id: 3306-6
    detail.hit.zdb_id: 1476593-7
    SSG: 5,21
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages