Characterization of a diester lipase activity in human erythrocytes.

Abstract:

:A diester lipase activity is described in human red blood cells (RBC). Diester lipase activity acts as a membrane-bound enzyme and is assayed using intact RBC as the enzyme source. An emulsion of di-[3H]-oleoylglycerol (0.6 mM) serves as the substrate. The optimum pH for the reaction is 7.8 at 37 degrees C. Lipolytic rates are monitored by quantitation of the amount of [3H]-oleic acid released during 20 min of incubation after a two-step purification procedure. [3H]-oleic acid is first extracted from the incubation mixture by means of a liquid-liquid partition system and further isolated by thin-layer chromatography. Suspensions of purified RBC obtained from 36 healthy adult subjects had a diester lipase activity of 196 +/- (SD) 45 mU/10(12) RBC, with no difference between men and women.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Somma C,Arnaud J,Boyer J

doi

10.1159/000206770

subject

Has Abstract

pub_date

1983-01-01 00:00:00

pages

337-40

issue

5

eissn

0001-5792

issn

1421-9662

journal_volume

70

pub_type

杂志文章
  • Immunological analysis of acquired factor VIII inhibitor in a case with immunologic disorder.

    abstract::Coagulation factor VIII inhibitor arising in a patient with autoimmune disease was immunologically analyzed. A 63-year-old man who had been diagnosed as suffering from polyarteritis nodosa was treated with prednisolone for 10 years. Severe bleeding tendency developed and coagulation studies demonstrated a high titer o...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204879

    authors: Okamura T,Yamauchi Y,Fukuda T,Suehiro K,Murakawa M,Shibuya T,Nagasawa K,Harada M,Niho Y

    更新日期:1991-01-01 00:00:00

  • Defective terminal maturation along monocyte-macrophage lineage in chronic myelomonocytic leukemia.

    abstract::The maturation process of leukemic myelomonocytoid cells derived from peripheral blood of two typical cases of chronic myelomonocytic leukemia was investigated in vitro. In both cases, liquid culture of the leukemic cells in the presence or absence of 12-o-tetradecanoyl phorbol-13-acetate yielded either monocyte-macro...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206382

    authors: Takuwa N,Kanegasaki S,Asano S,Tomita T,Nakayama E,Sato N,Shinohara T,Miwa S

    更新日期:1984-01-01 00:00:00

  • Chronic lymphocytic leukemia in Maghreb and Europe. A comparison between Algiers and Amiens from 1966 to 1976.

    abstract::The frequency of chronic lymphocytic leukemia (CLL) varies a great deal from one population to another. We have undertaken to compare the aspects of CLL in Maghreb and Europe through two series of comparable importance, studied during the same period and under similar conditions in Algiers and Amiens. This comparison ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206896

    authors: Bellabes S,Hamman P,Desablens B,Colonna P,Messerschmitt J

    更新日期:1983-01-01 00:00:00

  • Primary fibrinolysis and spontaneous rupture of the spleen in acute lymphoblastic leukemia.

    abstract::A 51-year-old male with acute lymphoblastic leukemia whose course was complicated by primary fibrinolysis and spontaneous rupture of the spleen is described. The patient was treated with various drug combinations: vincristine and prednisone, later by cytosine arabinoside and finally by prednisone, methotrexate and 6-m...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207962

    authors: Gafter U,Mandel EM,Weiss S,Djaldetti M

    更新日期:1976-01-01 00:00:00

  • Hemolytic anemia in a patient with subacute bacterial endocarditis due to Streptococcus sanguis.

    abstract::We describe a case of hemolytic anemia with subacute bacterial endocarditis due to Streptococcus sanguis. The major hematological features of the patient were a normocytic anemia with reticulocytosis, an elevation of serum lactate dehydrogenase, and a marked reduction of serum haptoglobin. All these signs of hemolytic...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000203981

    authors: Inada T,Shirono K,Tsuda H

    更新日期:1995-01-01 00:00:00

  • Nonsecretory myeloma: a study on hypoimmunoglobulinemia.

    abstract::In evaluating hypoimmunoglobulinemia in a patient with nonsecretory myeloma, studies of in vitro immunoglobulin synthesis were performed during a 3-year period. Impaired polyclonal response to mitogen stimulation associated with excessive suppressor activity was demonstrable at diagnosis. Despite successful chemothera...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205622

    authors: Shustik C,Michel R,Karsh J

    更新日期:1988-01-01 00:00:00

  • Effect of granulocyte/colony-stimulating factor on the onset of the adult respiratory distress syndrome.

    abstract::To evaluate the effect of granulocyte/colony-stimulating factor (G-CSF) on the onset of the adult respiratory distress syndrome (ARDS), we investigated whether the incidence of ARDS due to pulmonary infection differed between the G-CSF group which received chemotherapy with G-CSF and historical controls without G-CSF....

    journal_title:Acta haematologica

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1159/000040937

    authors: Takahashi Y,Kobayashi Y,Chikayama S,Ikeda M,Kondo M

    更新日期:1999-01-01 00:00:00

  • A severe case of cefoxitin-induced immune hemolytic anemia.

    abstract::Drug-induced immune hemolytic anemia is a rare but underdiagnosed and potentially fatal condition. We report a case of severe hemolytic anemia induced by cefoxitin in a 45-year-old woman admitted with menometrorrhagia. Hemoglobin levels reached a nadir of 4.7 g/dl approximately 72 h after cefoxitin initiation, and hem...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000320169

    authors: Leaf DE,Langer NB,Markowski M,Garratty G,Diuguid DL

    更新日期:2010-01-01 00:00:00

  • Levamisole and autoimmunity in angioimmunoblastic lymphadenopathy.

    abstract::A case of angioimmunoblastic lymphadenopathy (AILD) with important autoimmune symptoms disappearing under Levamisole therapy is reported. Since Levamisole is thought to have no direct effect on B cells, it is supposed that in AILD it regulates B lymphocyte activity via the restoration of impaired T cell functions. ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207551

    authors: Andrieu JM,Youinou P,Herzog C

    更新日期:1979-01-01 00:00:00

  • Primary extranodal non-Hodgkin's lymphoma of the vagina: a case report and a review of the literature.

    abstract::Primary lymphoma of the female genital tract is very rare. We report the case of a 36-year-old woman who was referred to our hospital because of an indeterminate Pap smear test. The colposcopy showed a thickening of the posterior vaginal wall and various irregular ulcerated nodular lesions. Histological examination, i...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000337336

    authors: Guastafierro S,Tedeschi A,Criscuolo C,Celentano M,Cobellis L,Rossiello R,Falcone U

    更新日期:2012-01-01 00:00:00

  • Scanning immunoelectron microscopy of hairy cell leukemia.

    abstract::Scanning electron microscopy has shown a typical cell surface morphology in hairy cell leukemia. Scanning immunoelectron microscope techniques, utilizing monoclonal antibodies and colloidal gold particles, have recently become available. Eight patients with hairy cell leukemia have been studied with a panel of monoclo...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206218

    authors: Soligo D,Lambertenghi-Deliliers G,Nava MT,Polli N,Cattoretti G,Polli EE

    更新日期:1985-01-01 00:00:00

  • Congenital combined defects of factor VII: a critical review.

    abstract::Factor VII deficiency is the least rare among uncommon congenital coagulation disorders. The majority of cases are isolated deficiencies. In some cases, FVII deficiency has been found to be associated with the deficiency in another coagulation factor or with non-coagulation-related abnormalities or defects. The evalua...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000096789

    authors: Girolami A,Ruzzon E,Tezza F,Allemand E,Vettore S

    更新日期:2007-01-01 00:00:00

  • Variations in morphological and immunological blast cell phenotype in a case of acute leukaemia with t(4;11) translocation.

    abstract::A case of acute leukaemia with t(4;11) chromosomal abnormality in a 28-year-old woman is reported. At diagnosis, two blast cell populations were seen: 60% of the cells were small cells with lymphoid morphology, 40% were large cells with monocytic morphology. Cytochemical examination was consistent with acute myeloid l...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206046

    authors: Campos L,Espinouse D,Felman P,Charrin C,Gentilhomme O,Germain D

    更新日期:1986-01-01 00:00:00

  • Recombinant alpha-interferons, thyroid irradiation and thyroid disease.

    abstract::Recombinant alpha-interferons are used as therapeutic agents in an increasing number of benign and malignant disorders. Long-term administration of recombinant alpha-interferon as a maintenance agent is associated with a small number of adverse side-effects which are responsible for patient intolerance of this drug. T...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204881

    authors: Giles FJ,Worman CP,Jewell AP,Goldstone AH

    更新日期:1991-01-01 00:00:00

  • Platelet aggregation in diabetic retinopathy.

    abstract::Platelet aggregation in diabetic retinopathy was investigated in a group of 25 patients. An enhanced activity induced by epinephrine and arachidonic acid was found in this group as compared with the controls, whereas in adenosine diphosphate (ADP) platelet aggregation no differences were observed. Spontaneous aggregat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207695

    authors: Creter D,Pavlotzky F,Savir H

    更新日期:1978-01-01 00:00:00

  • Allogeneic bone marrow transplantation in multiple myeloma.

    abstract::A 28-year-old woman with Bence-Jones multiple myeloma (MM) presented with several osteolytic lesions and a massive bone marrow infiltration with mature plasmocytes. After 6 cycles of chemotherapy with melphalan and prednisone, the patient, in apparent clinical remission, underwent allogeneic bone marrow transplantatio...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000205969

    authors: Gallamini A,Buffa F,Bacigalupo A,Van Lint MT,Peralvo J,Pittaluga PA,Occhini D,Marmont AM

    更新日期:1987-01-01 00:00:00

  • The significance of minimal residual disease in stem cell grafts and the role of purging: is it better to purge in vivo or in vitro?

    abstract::Contamination of autologous graft by tumor, in addition to incomplete tumor eradication, can partly explain why relapse remains the commonest cause of treatment failure after autologous stem cell transplantation (ASCT) in patients with malignant hematologic disorders. Monitoring of minimal residual disease (MRD) is no...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000088411

    authors: Melillo L,Cascavilla N,Lerma E,Corsetti MT,Carella AM

    更新日期:2005-01-01 00:00:00

  • Remission induction of refractory anaemia with excess blasts in transformation by sole treatment with granulocyte colony-stimulating factor with persistent chromosomal abnormality.

    abstract::We report a patient with myelodysplastic syndrome (MDS), refractory anaemia with excess blasts in transformation, in whom complete remission (CR) was achieved with the administration of granulocyte colony-stimulating factor (G-CSF). The 76-year-old patient was admitted to our hospital with a fever and a productive cou...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000057637

    authors: Kondo H,Kasahara Y,Mori A

    更新日期:2002-01-01 00:00:00

  • Coagulation Disturbances in Patients with Argininemia.

    abstract:BACKGROUND:Argininemia is an autosomal recessive urea cycle disorder (UCD). Unlike other UCD, hyperammonemia is rarely seen. Patients usually present in childhood with neurological symptoms. Uncommon presentations like neonatal cholestasis or cirrhosis have been reported. Although transient elevations of liver transami...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000493678

    authors: Kiykim E,Zubarioglu T,Cansever MS,Celkan T,Häberle J,Aktuglu Zeybek AC

    更新日期:2018-01-01 00:00:00

  • Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.

    abstract:OBJECTIVE:To investigate a family with factor VII (FVII) deficiency from Argentina. PATIENTS AND METHODS:The proposita is a 14-year-old girl who presented with a mild to moderate bleeding tendency. Menorrhagia is controlled with periodical administration of small doses of recombinant FVII concentrate. The mother of th...

    journal_title:Acta haematologica

    pub_type:

    doi:10.1159/000507071

    authors: Girolami A,Paoletti M,Ferrari S,Garcia D

    更新日期:2021-01-01 00:00:00

  • Beta-thromboglobulin levels in relation to myocardial infarction--preliminary observations.

    abstract::34 patients with myocardial infarction were studied with daily measurements of beta-thromboglobulin (BTG) and 125I fibrinogen scanning in order to detect deep-venous thrombosis (DVT). Serial levels of BTG were unhelpful in the early detection of this condition, which occurred in 7 of the patients studied. 5 of the pat...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207238

    authors: Simmonds JP,O'Malley BP,Maskill MR,O'Connor JF,Burridge DJ

    更新日期:1980-01-01 00:00:00

  • Hemophagocytosis simulating malignant histiocytosis: a terminal event of the myelodysplastic syndrome.

    abstract::We describe a patient with hemophagocytic syndrome resembling malignant histiocytosis which was complicating myelodysplastic disease of 3 years duration. Detailed morphological and ultrastructural studies indicate that the histiocytic component did not demonstrate features of malignancy. A review of other known malign...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000206198

    authors: Prokocimer M,Inbal A,Gelber M,Shohat B,Ben Basat M,Shaklai M

    更新日期:1985-01-01 00:00:00

  • A new case of IgE myeloma.

    abstract::A new case of IgE myeloma is described. A 77-year-old woman presented with bone pain and fatigue. Serum protein analysis revealed a paraprotein of the IgE kappa type; bone marrow aspirate and immunofluorescence confirmed the diagnosis; ultrastructural examination showed immature plasma cells. Treatment with prednisone...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204851

    authors: Invernizzi F,Monti G,Caviglia AG,Meroni P,Zanussi C

    更新日期:1991-01-01 00:00:00

  • Acute transformation of chronic large granular lymphocyte leukemia into an aggressive form associated with preferential organ involvement.

    abstract::In most patients with large granular lymphocyte (LGL) leukemia, the disease appears to progress slowly if at all, and no therapy is generally required. We present a patient with CD3+ CD8+ CD16+ LGL leukemia, who showed a benign clinical course for more than 7 months without therapy, but subsequently developed aggressi...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204336

    authors: Matsubara A,Matsumoto M,Takada K,Hato T,Hasegawa H,Tamai T,Yasukawa M,Fujita S

    更新日期:1994-01-01 00:00:00

  • L-gamma-glutamyl transpeptidase activity in normal and leukemic leukocytes.

    abstract::The activity of gamma-glutamyl transpeptidase was investigated in normal and leukemia leukocytes. Enzyme activity was positively correlated with the proportion of mature neutrophils and monocytes. In isolated leukocytes from patients with acute myeloid leukemia low values were obtained compared to controls. ...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207384

    authors: Hultberg B,Sjögren U

    更新日期:1980-01-01 00:00:00

  • Impairment of platelet adhesiveness and platelet factor 3 activity in cyanotic congenital heart disease.

    abstract::In 33 children with cyanotic congenital heart disease the platelet function has been studied. The most significant changes were reduced platelet adhesiveness to glass and impaired availability of platelet factor 3 in nearly 50% of the patients. Although clot retraction was poor in 84% of them, thrombocytopenia and pro...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000208017

    authors: Bhargava M,Sanyal SK,Thapar MK,Kumar S,Hooja V

    更新日期:1976-01-01 00:00:00

  • Acute promyelocytic leukemia in childhood. Report of a case with a review of the literature.

    abstract::A rare case of acute promyelcytic leukemia (APL) is reported in a 7-year-old boy. The patient displayed the typical features of APL including impaction of the marrow with promyelocytes, marked elevation of the serum vitamin B12 and transcobalamin I levels and a hemorrhagic diathesis. The bleeding diathesis in the case...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000207589

    authors: Engelhard D,Yatziv S,Rachmilewitz EA,Polliack A

    更新日期:1979-01-01 00:00:00

  • Monosomy 7 myelodysplasia in childhood. Two case reports.

    abstract::Monosomy 7 myelodysplasia is a rare hematological entity and is associated with morphological abnormalities in bone marrow and peripheral smear, and poor prognosis in children. We describe 2 children with infantile monosomy 7 myelodysplasia which evolved to leukemia. One of them died after 1 month, and the other is st...

    journal_title:Acta haematologica

    pub_type: 杂志文章

    doi:10.1159/000204135

    authors: Yeşilipek MA,Lüleci G,Velipaşaoğlu S,Berker S,Yeğin O

    更新日期:1994-01-01 00:00:00

  • Roles of hematopoietic transcription factors GATA-1 and GATA-2 in the development of red blood cell lineage.

    abstract::The transcription factors GATA-1 and GATA-2 play key roles in gene regulation during erythropoiesis. Gene ablation studies in mouse revealed that GATA-2 is crucial for the maintenance and proliferation of immature hematopoietic progenitors, whereas GATA-1 is essential for the survival of erythroid progenitors as well ...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000065660

    authors: Ohneda K,Yamamoto M

    更新日期:2002-01-01 00:00:00

  • Biologic nature of the myelodysplastic syndromes.

    abstract::In the myelodysplastic syndromes (MDS) clonogenic marrow cell culture studies have demonstrated intrinsic hemopoietic stem cell and progenitor cell abnormalities consistent with these disorders representing clonal hemopathies. Abnormal responsiveness of these cells to stimulatory and inhibitory growth factors indicate...

    journal_title:Acta haematologica

    pub_type: 杂志文章,评审

    doi:10.1159/000205911

    authors: Greenberg PL

    更新日期:1987-01-01 00:00:00