Factor VIII-induced superaggregation of human platelets.

Abstract:

:High concentrations of bovine factor VIII cause clumping of platelets into a few very large aggregates. This response is termed superaggregation. It is distinct from factor-VIII-induced agglutination but is also independent of both extracellular calcium ions and platelet energy metabolism. Neither agglutinating lectins nor aggregating agents, including thrombin, ADP, the ionophore A23187, and U46619, a prostaglandin analog, can induce superaggregation, even at very high concentrations. Washed platelets undergo superaggregation, and superaggregation does not increase the amounts of fibrinogen or albumin trapped by agglutinated platelets. It is not inhibited by membrane-stabilizing drugs or by colchicine or cytochalasin-B. Formaldehyde and glutaraldehyde prevent superaggregation without affecting the binding of radiolabeled factor VIII to the platelets. Superaggregated platelets are separated by approximately 50 nm and are not shape-changed or degranulated. In adenosine diphosphate (ADP) induced aggregation, the platelets are distorted and only 30 nm apart. Superaggregation is reversed by dextran sulfate, and the dispersed platelets are still able to respond to ADP. Our observations are consistent with the binding of high molecular weight multimers of bovine factor VIII to more than one receptor on each platelet, with superaggregation occurring through recruitment of additional receptors. This process may be interrupted by protein crosslinking reagents, such as formaldehyde and glutaraldehyde.

journal_name

Blood

journal_title

Blood

authors

Kirby EP,Mills DC,Holmsen H,Russo M

subject

Has Abstract

pub_date

1982-12-01 00:00:00

pages

1359-69

issue

6

eissn

0006-4971

issn

1528-0020

journal_volume

60

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Metalloproteinase inhibition and erythroid potentiation are independent activities of tissue inhibitor of metalloproteinases-1.

    abstract::Tissue inhibitor of metalloproteinases-1 (TIMP-1), the major physiological matrix metalloproteinase inhibitor and a potent antimetastatic factor, also stimulates the growth of erythroid progenitors (erythroid-potentiating activity). We analyzed the relationship between the growth factor activity and protease inhibitio...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chesler L,Golde DW,Bersch N,Johnson MD

    更新日期:1995-12-15 00:00:00

  • Hydroxyl radical formation by sickle erythrocyte membranes: role of pathologic iron deposits and cytoplasmic reducing agents.

    abstract::Sickle erythrocyte (RBC) membranes were previously shown to manifest increased Fenton activity (iron-dependent, peroxide-driven formation of hydroxyl radical [.OH]) compared with normal RBC membranes, but the nature of the catalytic iron was not defined. We now find that sickle membranes exposed to superoxide (.O2-) a...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Repka T,Hebbel RP

    更新日期:1991-11-15 00:00:00

  • Core 2 branching beta1,6-N-acetylglucosaminyltransferase and high endothelial cell N-acetylglucosamine-6-sulfotransferase exert differential control over B- and T-lymphocyte homing to peripheral lymph nodes.

    abstract::Blood-borne lymphocyte trafficking to peripheral lymph nodes (PLNs) depends on the successful initiation of rolling interactions mediated by L-selectin binding to sialomucin ligands in high endothelial venules (HEVs). Biochemical analysis of purified L-selectin ligands has identified posttranslational modifications me...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-05-1986

    authors: Gauguet JM,Rosen SD,Marth JD,von Andrian UH

    更新日期:2004-12-15 00:00:00

  • Peripheral blood stem cell allograft rejection mediated by CD4(+) T lymphocytes recognizing a single mismatch at HLA-DP beta 1*0901.

    abstract::Little is known about the molecular characteristics of alloantigens recognized by alloreactive T cells mediating hematologic stem cell graft rejection. In particular, it has never been shown that such alloantigens can be encoded by HLA-DP beta alleles. Indeed, matching for HLA-DP antigens is generally not considered t...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.4.1122

    authors: Fleischhauer K,Zino E,Mazzi B,Sironi E,Servida P,Zappone E,Benazzi E,Bordignon C

    更新日期:2001-08-15 00:00:00

  • Characterization of DNA-binding-dependent and -independent functions of SCL/TAL1 during human erythropoiesis.

    abstract::The transcription factor TAL1 has major functions during embryonic hematopoiesis and in adult erythropoiesis and megakaryocytopoiesis. These functions rely on different TAL1 structural domains that are responsible for dimerization, transactivation, and DNA binding. Previous work, most often done in mice, has shown tha...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-05-1689

    authors: Ravet E,Reynaud D,Titeux M,Izac B,Fichelson S,Roméo PH,Dubart-Kupperschmitt A,Pflumio F

    更新日期:2004-05-01 00:00:00

  • Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells.

    abstract::Hypersensitivity to cross-linking agents and predisposition to malignancy are characteristic of the genetically heterogeneous inherited bone marrow failure syndrome, Fanconi anemia (FA). The protein encoded by the recently cloned FA complementation group A gene, FAA, has been expected to localize in the nucleus as bas...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kruyt FA,Waisfisz Q,Dijkmans LM,Hermsen MA,Youssoufian H,Arwert F,Joenje H

    更新日期:1997-11-01 00:00:00

  • Uniparental disomies, homozygous deletions, amplifications, and target genes in mantle cell lymphoma revealed by integrative high-resolution whole-genome profiling.

    abstract::Mantle cell lymphoma (MCL) is genetically characterized by the t(11;14)(q13;q32) translocation and a high number of secondary chromosomal alterations. However, only a limited number of target genes have been identified. We have studied 10 MCL cell lines and 28 primary tumors with a combination of a high-density single...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-07-170183

    authors: Beà S,Salaverria I,Armengol L,Pinyol M,Fernández V,Hartmann EM,Jares P,Amador V,Hernández L,Navarro A,Ott G,Rosenwald A,Estivill X,Campo E

    更新日期:2009-03-26 00:00:00

  • Coinfection of multiple strains of Epstein-Barr virus in immunocompetent normal individuals: reassessment of the viral carrier state.

    abstract::This study reassesses the occurrence of Epstein-Barr virus (EBV) diversity and coinfection versus dominance of a single viral strain within immunocompetent normal carriers. Polymerase chain reaction analysis of several different polymorphic loci of the EBV genome was performed on collections of peripheral blood mononu...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Srivastava G,Wong KY,Chiang AK,Lam KY,Tao Q

    更新日期:2000-04-01 00:00:00

  • Cellular response to hypoxia involves signaling via Smad proteins.

    abstract::The transforming growth factor-beta (TGF-beta) family of cytokines regulates vascular development and inflammatory responses. We have recently shown that exposure of human umbilical vein endothelial cells (HUVECs) to hypoxia (1% O(2)) increases gene expression and bioactivation of TGF-beta2 and induces its downstream ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-02-0629

    authors: Zhang H,Akman HO,Smith EL,Zhao J,Murphy-Ullrich JE,Batuman OA

    更新日期:2003-03-15 00:00:00

  • Efficacy of daunorubicin in the therapy of adult acute lymphocytic leukemia: a prospective randomized trial by cancer and leukemia group B.

    abstract::The efficacy of the addition of intensive therapy with daunorubicin (45 mg/m2 IV on days 1, 2, 3) to an otherwise identical induction program consisting of vincristine, prednisone, and L-asparaginase was assessed in 177 previously untreated adults (greater than or equal to 20 years of age) with acute lymphocytic leuke...

    journal_title:Blood

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:

    authors: Gottlieb AJ,Weinberg V,Ellison RR,Henderson ES,Terebelo H,Rafla S,Cuttner J,Silver RT,Carey RW,Levy RN

    更新日期:1984-07-01 00:00:00

  • Fibrinogen Birmingham: a heterozygous dysfibrinogenemia (A alpha 16 Arg----His) containing heterodimeric molecules.

    abstract::Fibrinogen was isolated from the plasma of a 25-year-old female with a history of mild bleeding and several recent moderate to severe hemorrhagic episodes. Coagulability with thrombin approached 100% and varied directly with the time of incubation with the enzyme. High-performance liquid chromatography analysis of thr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Siebenlist KR,Prchal JT,Mosesson MW

    更新日期:1988-03-01 00:00:00

  • Hepatosplenic T-cell lymphoma: a rare but challenging entity.

    abstract::Hepatosplenic T-cell lymphoma (HSTCL) is a rare T-cell neoplasm that most commonly arises from a small subset of γ/δ T-cell receptor-expressing lymphocytes. HSTCL is more common in adolescent and young adults and has a rapidly progressive clinical course and poor outcome due to its refractoriness to conventional chemo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2019004118

    authors: Pro B,Allen P,Behdad A

    更新日期:2020-10-29 00:00:00

  • Total folate binding capacity of normal human plasma, and variations in uremia, cirrhosis, and pregnancy.

    abstract::The current study presents evidence that all human serum contains a class of high-affinity folate binders (KA=2.8 X10(10 liters/mole), which migrate as a single peak on gel filtration. Failure of previous studies to detect this characteristic in all but a minority of subjects is attributable to its variable, often tot...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Colman N,Herbert V

    更新日期:1976-12-01 00:00:00

  • Gene expression profiling of human plasma cell differentiation and classification of multiple myeloma based on similarities to distinct stages of late-stage B-cell development.

    abstract::To identify genes linked to normal plasma cell (PC) differentiation and to classify multiple myeloma (MM) with respect to the expression patterns of these genes, we analyzed global mRNA expression in CD19-enriched B cells (BCs) from 7 tonsils, CD138-enriched PCs from 11 tonsils, 31 normal bone marrow samples, and 74 M...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-06-1737

    authors: Zhan F,Tian E,Bumm K,Smith R,Barlogie B,Shaughnessy J Jr

    更新日期:2003-02-01 00:00:00

  • Self-renewal in late-stage erythropoiesis.

    abstract::Extensive in vitro self-renewal of proerythroblasts from the earliest period of definitive erythropoiesis, as reported by England and co-investigators in this issue of Blood, expands the potential role of self-renewal in mammalian hematopoiesis and suggests a possible source of blood cells for clinical treatments. ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2010-12-324319

    authors: Koury MJ

    更新日期:2011-03-03 00:00:00

  • Human hematopoietic stem cells stimulated to proliferate in vitro lose engraftment potential during their S/G(2)/M transit and do not reenter G(0).

    abstract::An understanding of mechanisms regulating hematopoietic stem cell engraftment is of pivotal importance to the clinical use of cultured and genetically modified transplants. Human cord blood (CB) cells with lymphomyeloid repopulating activity in NOD/SCID mice were recently shown to undergo multiple self-renewal divisio...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Glimm H,Oh IH,Eaves CJ

    更新日期:2000-12-15 00:00:00

  • CD62L expression identifies a unique subset of polyfunctional CD56dim NK cells.

    abstract::Human natural killer (NK) cells comprise 2 main subsets, CD56(bright) and CD56(dim) cells, that differ in function, phenotype, and tissue localization. To further dissect the heterogeneity of CD56(dim) cells, we have performed transcriptome analysis and functional ex vivo characterization of human NK-cell subsets acco...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-11-253286

    authors: Juelke K,Killig M,Luetke-Eversloh M,Parente E,Gruen J,Morandi B,Ferlazzo G,Thiel A,Schmitt-Knosalla I,Romagnani C

    更新日期:2010-08-26 00:00:00

  • Neutral tumor evolution in myeloma is associated with poor prognosis.

    abstract::Recent studies suggest that the evolutionary history of a cancer is important in forecasting clinical outlook. To gain insight into the clonal dynamics of multiple myeloma (MM) and its possible influence on patient outcomes, we analyzed whole exome sequencing tumor data for 333 patients from Myeloma XI, a UK phase 3 t...

    journal_title:Blood

    pub_type: 杂志文章,随机对照试验

    doi:10.1182/blood-2016-11-750612

    authors: Johnson DC,Lenive O,Mitchell J,Jackson G,Owen R,Drayson M,Cook G,Jones JR,Pawlyn C,Davies FE,Walker BA,Wardell C,Gregory WM,Cairns D,Morgan GJ,Houlston RS,Kaiser MF

    更新日期:2017-10-05 00:00:00

  • Correction of abnormal T-cell receptor repertoire during interferon-alpha therapy in patients with hairy cell leukemia.

    abstract::Patients with the B-cell malignancy hairy cell leukemia (HCL) exhibit a skewed T-cell repertoire with oligoclonal expression or absence of many members of the T-cell receptor (TCR) BV gene families. To evaluate whether interferon-alpha (IFN-alpha) therapy would not only restore normal hematopoiesis, but also the abnor...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kluin-Nelemans HC,Kester MG,van deCorput L,Boor PP,Landegent JE,van Dongen JJ,Willemze R,Falkenburg JH

    更新日期:1998-06-01 00:00:00

  • Vaccination of human subjects expands both specific and bystander memory T cells but antibody production remains vaccine specific.

    abstract::Human subjects maintain long-term immunologic memory against infective organisms but the mechanism is unclear. CD4+ T-helper memory (Thmem) cells are pivotal in controlling humoral and cellular responses, therefore their longevity and response to vaccination are critical for maintenance of protective immunity. To prob...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-08-3255

    authors: Di Genova G,Roddick J,McNicholl F,Stevenson FK

    更新日期:2006-04-01 00:00:00

  • Improvement in quality of life of patients with AL amyloidosis treated with high-dose melphalan and autologous stem cell transplantation.

    abstract::Treatment of AL amyloidosis patients with high-dose melphalan chemotherapy followed by autologous peripheral blood stem cell transplantation (HDM/SCT) can produce hematologic complete responses (CRs) and improvement in organ function. To determine whether these responses are accompanied by improvement in quality of li...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:10.1182/blood-2004-01-0089

    authors: Seldin DC,Anderson JJ,Sanchorawala V,Malek K,Wright DG,Quillen K,Finn KT,Berk JL,Dember LM,Falk RH,Skinner M

    更新日期:2004-09-15 00:00:00

  • Hoechst 33342 efflux identifies a subpopulation of cytogenetically normal CD34(+)CD38(-) progenitor cells from patients with acute myeloid leukemia.

    abstract::Efflux of Hoechst 33342 from normal hematopoietic cells identifies a "side population" (SP(+)) of negatively staining cells that, in the mouse, are largely CD34(-) and are enriched for primitive progenitors. To further characterize human SP(+) cells, blood or bone marrow from 16 patients with acute myeloid leukemia (A...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v97.12.3882

    authors: Feuring-Buske M,Hogge DE

    更新日期:2001-06-15 00:00:00

  • Mitochondrial membrane sensitivity to depolarization in acute myeloblastic leukemia is associated with spontaneous in vitro apoptosis, wild-type TP53, and vicinal thiol/disulfide status.

    abstract::Nonresponse to remission-induction chemotherapy, which remains a major problem in acute myeloblastic leukemia (AML), has been linked to cellular resistance to apoptosis. Because the apoptosis induced by chemotherapeutic drugs is mediated by loss of mitochondrial transmembrane potential (MTP), it was postulated that se...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.2.405

    authors: Pallis M,Grundy M,Turzanski J,Kofler R,Russell N

    更新日期:2001-07-15 00:00:00

  • The manipulation of miRNA-gene regulatory networks by KSHV induces endothelial cell motility.

    abstract::miRNAs have emerged as master regulators of cancer-related events. miRNA dysregulation also occurs in Kaposi sarcoma (KS). Exploring the roles of KS-associated miRNAs should help to identify novel angiogenesis and lymphangiogenesis pathways. In the present study, we show that Kaposi sarcoma-associated herpesvirus (KSH...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-01-330589

    authors: Wu YH,Hu TF,Chen YC,Tsai YN,Tsai YH,Cheng CC,Wang HW

    更新日期:2011-09-08 00:00:00

  • A unique 7p/12q chromosomal abnormality associated with recurrent abortion and hypofibrinogenemia.

    abstract::Recurrent first trimester abortions led to evaluation of a 25-year-old woman. Studies revealed she had hypofibrinogenemia (68 mg/dL) without evidence of dysfibrinogenemia or increased fibrinogen turnover. She was also found to have a unique 46,XX, t(7;12) (p 15.2;q24.31) karyotype. Hypofibrinogenemia and identical chr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kitchens CS,Cruz AC,Kant JA

    更新日期:1987-10-01 00:00:00

  • A naturally occurring E30Q mutation in the Gla domain of protein Z causes its impaired secretion and subsequent deficiency.

    abstract::Protein Z is a vitamin K-dependent glycoprotein that plays a role in the regulation of coagulation. A nucleotide substitution of G by C in exon II of the protein Z gene, resulting in the replacement of Glu-30 with Gln (E30Q), and a G to A transition at the 79th nucleotide in intron F (IntF79G/A) were heterozygously id...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-06-2250

    authors: Souri M,Koseki-Kuno S,Iwata H,Kemkes-Matthes B,Ichinose A

    更新日期:2005-04-15 00:00:00

  • Innate immunity defects in Hermansky-Pudlak type 2 syndrome.

    abstract::Adaptor protein-3 (AP-3) is an ubiquitous cytoplasmic complex that shuttles cargo proteins from the trans-Golgi and a tubular-endosomal compartment to endosome-lysosome-related organelles. Lack of the beta3A subunit of this complex causes Hermansky-Pudlak syndrome type 2, an autosomal recessive disease characterized b...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-11-4398

    authors: Fontana S,Parolini S,Vermi W,Booth S,Gallo F,Donini M,Benassi M,Gentili F,Ferrari D,Notarangelo LD,Cavadini P,Marcenaro E,Dusi S,Cassatella M,Facchetti F,Griffiths GM,Moretta A,Notarangelo LD,Badolato R

    更新日期:2006-06-15 00:00:00

  • Erythropoietin receptor haploinsufficiency and in vivo interplay with granulocyte-macrophage colony-stimulating factor and interleukin 3.

    abstract::Erythropoietin (EPO) and its receptor (EPOR) are critical for definitive erythropoiesis, as mice lacking either gene product die during embryogenesis with severe anemia. Here we demonstrate that mice expressing just one functional allele of the EpoR have lower hematocrits and die more frequently than do wild-type litt...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v99.7.2603

    authors: Jegalian AG,Acurio A,Dranoff G,Wu H

    更新日期:2002-04-01 00:00:00

  • Characteristics and outcomes of patients with chronic myeloid leukemia and T315I mutation following failure of imatinib mesylate therapy.

    abstract::Chronic myeloid leukemia (CML) with T315I mutation has been reported to have poor prognosis. We analyzed 27 patients with T315I, including 20 who developed T315I after imatinib failure (representing 11% of 186 patients with imatinib failure), and 7 of 23 who developed new mutations after second tyrosine kinase inhibit...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-11-123950

    authors: Jabbour E,Kantarjian H,Jones D,Breeden M,Garcia-Manero G,O'Brien S,Ravandi F,Borthakur G,Cortes J

    更新日期:2008-07-01 00:00:00

  • Increasing hepatitis C virus RNA levels in hemophiliacs: relationship to human immunodeficiency virus infection and liver disease. Multicenter Hemophilia Cohort Study.

    abstract::We have previously observed an increased frequency of liver failure in human immunodeficiency virus (HIV)-infected hemophiliacs. The purpose of this study was to quantitate hepatitis C virus (HCV) RNA levels in serial samples from HIV-seropositive (HIV+) and HIV-seronegative (HIV-) hemophiliacs before and after HIV se...

    journal_title:Blood

    pub_type: 杂志文章,多中心研究

    doi:

    authors: Eyster ME,Fried MW,Di Bisceglie AM,Goedert JJ

    更新日期:1994-08-15 00:00:00