Expression of plasma glutathione peroxidase in human liver in addition to kidney, heart, lung, and breast in humans and rodents.

Abstract:

:We analyzed the expression of plasma glutathione peroxidase (GSHPx-P) messenger RNA (mRNA) in mouse, rat, and human tissues, using a human GSHPx-P cDNA clone as the probe. Unlike the classical cellular glutathione peroxidase (GSHPx-1), GSHPx-P expression appears to be tissue-specific. In the mouse and rat, kidney expresses an mRNA at a high level detected with the human probe. A signal is also detected in mRNA isolated from mouse and rat heart, rat cardiac myocytes, mouse lung, epididymis, and the mammary gland of midpregnant mice. No signal is detected in mRNA isolated from mouse and rat liver, mouse brain, uterus, and testis. In human tissues, an mRNA hybridizing to GSHPx-P cDNA is present in liver, as well as kidney, heart, lung, breast, and placenta. We have shown that human kidney expresses a GSHPx-P mRNA, and not a GSHPx-P-like message, by isolating a cDNA clone from a human kidney library in lambda gt11. From the 412-nucleotide partial sequence of the kidney cDNA, which codes for the 40-170 amino acids of GSHPx-P including the TGA codon for selenocysteine, we found complete sequence identity of the kidney cDNA with GSHPx-P isolated from placenta. The expression of GSHPx-P mRNA in cell lines was also studied. There is some correlation of the expression of GSHPx-P in these cell lines with that in normal tissues. Cell lines that expressed GSHPx-P mRNA or protein included the human hepatocarcinoma HepG2, Hep3B cells, human kidney carcinoma A498 cells, and the human breast cancer SK-BR-3, T47D, MDA-MB-231, and AdrrMCF-7 cells. Cell lines that did not express GSHPx-P included human choriocarcinoma BeWo cells, human breast cancer MCF-7, ZR-75-1, and Hs578T cells, and mouse hepatoma Hepa-1 cells.

journal_name

Blood

journal_title

Blood

authors

Chu FF,Esworthy RS,Doroshow JH,Doan K,Liu XF

subject

Has Abstract

pub_date

1992-06-15 00:00:00

pages

3233-8

issue

12

eissn

0006-4971

issn

1528-0020

journal_volume

79

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Detection of the carrier state for classic hemophilia using an enzyme-linked immunosorbent assay (ELISA).

    abstract::A high proportion of carriers of classic hemophilia can be identified in the laboratory because, in comparison to normal women, the concentration of antigens related to antihemophilic factor (AHF, factor VIII) that are detected in their plasma by heterologous antiserum (factor VIIIR:Ag) is relatively higher than the t...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Fishman DJ,Jones PK,Menitove JE,Ratnoff OD,Everson B

    更新日期:1982-06-01 00:00:00

  • RAR-alpha gene rearrangements as a genetic marker for diagnosis and monitoring in acute promyelocytic leukemia.

    abstract::Acute promyelocytic leukemias (APLs) are characterized by a translocation that involves chromosomes 15 and 17. The translocation breakpoints have recently been identified and shown to involve the RAR-alpha gene on 17 and myl on 15. Here we report Southern blotting analysis of 26 APLs, including cases with normal karyo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Biondi A,Rambaldi A,Alcalay M,Pandolfi PP,Lo Coco F,Diverio D,Rossi V,Mencarelli A,Longo L,Zangrilli D

    更新日期:1991-04-01 00:00:00

  • The microenvironment in mature B-cell malignancies: a target for new treatment strategies.

    abstract::Despite major therapeutic advances, most mature B-cell malignancies remain incurable. Compelling evidence suggests that crosstalk with accessory stromal cells in specialized tissue microenvironments, such as the bone marrow and secondary lymphoid organs, favors disease progression by promoting malignant B-cell growth ...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2009-06-225326

    authors: Burger JA,Ghia P,Rosenwald A,Caligaris-Cappio F

    更新日期:2009-10-15 00:00:00

  • Montreal platelet syndrome: a defect in calcium-activated neutral proteinase (calpain).

    abstract::Platelets from patients with Montreal platelet syndrome (MPS) consistently display a defect in the mechanisms that regulate platelet size during shape change and undergo spontaneous aggregation and stir-induced microaggregate formation. We now provide data that the surface glycoprotein composition of MPS platelets is ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Okita JR,Frojmovic MM,Kristopeit S,Wong T,Kunicki TJ

    更新日期:1989-08-01 00:00:00

  • Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles.

    abstract::Screening for hereditary hemochromatosis (HHC) by means of transferrin saturation (TS) levels has been advocated and will identify many patients who are asymptomatic. The purposes of this study were (1) to determine HFE genotypes among asymptomatic HHC patients and correlate this profile with the degree of iron overlo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Sham RL,Raubertas RF,Braggins C,Cappuccio J,Gallagher M,Phatak PD

    更新日期:2000-12-01 00:00:00

  • Receptors that induce erythroid differentiation of Ba/F3 cells: structural requirements and effect on STAT5 binding.

    abstract::Ectopic expression of the erythropoietin receptor (EpoR) in the interleukin-3 (IL-3)-dependent cell line Ba/F3 results in growth and partial erythroid differentiation in Epo. In contrast, introduction and activation of the interleukin-5 receptor (IL-5R) or of the granulocyte-macrophage colony-stimulating factor recept...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Pless M,Norga K,Carroll M,Heim MH,D'Andrea AD,Mathey-Prevot B

    更新日期:1997-05-01 00:00:00

  • Transcription factor Gfi-1 induced by G-CSF is a negative regulator of CXCR4 in myeloid cells.

    abstract::The mechanisms underlying granulocyte-colony stimulating factor (G-CSF)-induced mobilization of granulocytic lineage cells from the bone marrow to the peripheral blood remain elusive. We provide evidence that the transcriptional repressor growth factor independence-1 (Gfi-1) is involved in G-CSF-induced mobilization o...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-03-081448

    authors: De La Luz Sierra M,Gasperini P,McCormick PJ,Zhu J,Tosato G

    更新日期:2007-10-01 00:00:00

  • Necdin, a p53 target gene, regulates the quiescence and response to genotoxic stress of hematopoietic stem/progenitor cells.

    abstract::We recently defined a critical role for p53 in regulating the quiescence of adult hematopoietic stem cells (HSCs) and identified necdin as a candidate p53 target gene. Necdin is a growth-suppressing protein and the gene encoding it is one of several that are deleted in patients with Prader-Willi syndrome. To define th...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-11-393983

    authors: Asai T,Liu Y,Di Giandomenico S,Bae N,Ndiaye-Lobry D,Deblasio A,Menendez S,Antipin Y,Reva B,Wevrick R,Nimer SD

    更新日期:2012-08-23 00:00:00

  • HIF1α is required for survival maintenance of chronic myeloid leukemia stem cells.

    abstract::Hypoxia-inducible factor-1α (HIF1α), a master transcriptional regulator of the cellular and systemic hypoxia response, is essential for the maintenance of self-renewal capacity of normal HSCs. It is still unknown whether HIF1α has a role in survival regulation of leukemia stem cells (LSCs) in chronic myeloid leukemia ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-10-387381

    authors: Zhang H,Li H,Xi HS,Li S

    更新日期:2012-03-15 00:00:00

  • Transforming growth factor-beta regulates c-kit message stability and cell-surface protein expression in hematopoietic progenitors.

    abstract::The cell-surface receptor c-kit and its cognate ligand stem-cell factor (SCF) or steel factor (SLF) are important for the maintenance of hematopoiesis both in vitro and in vivo. Transforming growth factor-beta (TGF-beta) has been shown to be a potent inhibitor of SLF-mediated synergistic growth of murine Lin-Sca-1+ pr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Dubois CM,Ruscetti FW,Stankova J,Keller JR

    更新日期:1994-06-01 00:00:00

  • Anti-platelet factor 4/heparin antibodies in orthopedic surgery patients receiving antithrombotic prophylaxis with fondaparinux or enoxaparin.

    abstract::Heparin-induced thrombocytopenia (HIT) is caused by platelet-activating IgG antibodies that recognize platelet factor 4 (PF4) bound to heparin. Immunogenicity of heparins differs in that unfractionated heparin (UFH) induces more anti-PF4/heparin antibodies than low-molecular-weight heparin (LMWH) and UFH also causes m...

    journal_title:Blood

    pub_type: 杂志文章,随机对照试验

    doi:10.1182/blood-2005-05-1938

    authors: Warkentin TE,Cook RJ,Marder VJ,Sheppard JA,Moore JC,Eriksson BI,Greinacher A,Kelton JG

    更新日期:2005-12-01 00:00:00

  • Immunoproteasome down-modulation enhances the ability of dendritic cells to stimulate antitumor immunity.

    abstract::The process of dendritic cell (DC) maturation, critical for effective DC-based immunotherapy, also alters the proteasome such that peptides presented in the context of HLA class I are generated not by the constitutive proteasome, but by the immunoproteasome. Cytotoxic T lymphocytes (CTLs) induced by such DCs might not...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-04-083188

    authors: Dannull J,Lesher DT,Holzknecht R,Qi W,Hanna G,Seigler H,Tyler DS,Pruitt SK

    更新日期:2007-12-15 00:00:00

  • Reduction of the inhibitory antibody response to human factor VIII in hemophilia A mice by mutagenesis of the A2 domain B-cell epitope.

    abstract::Approximately 25% of patients with hemophilia A develop inhibitory antibodies after treatment with factor VIII. Most of the inhibitory activity is directed against epitopes in the A2 and C2 domains. Anti-A2 inhibitory antibodies recognize a 25-residue segment bounded by R484-I508. Several antigenic residues in this se...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-11-3891

    authors: Parker ET,Healey JF,Barrow RT,Craddock HN,Lollar P

    更新日期:2004-08-01 00:00:00

  • Src tyrosine kinase preactivation is associated with platelet hypersensitivity in essential thrombocythemia and polycythemia vera.

    abstract::Polycythemia vera (PV) and essential thrombocythemia (ET) are chronic myeloproliferative disorders characterized by an increased incidence of thrombo-hemorrhagic complications. The acquired somatic Janus kinase 2 (JAK2) V617F mutation is present in the majority of PV and ET patients. Because aberrant protein Tyr-phosp...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-12-196535

    authors: Randi ML,Brunati AM,Scapin M,Frasson M,Deana R,Magrin E,Fabris F,Donella-Deana A

    更新日期:2010-01-21 00:00:00

  • Simple electrophoretic system for presumptive identification of abnormal hemoglobins. By the International Committee for Standardization in Hematology.

    abstract::In order to determine if mutant hemoglobins can be identified by relatively simple methods, a Working Group of the ICSH Expert Panel on Abnormal Hemoglobins and Thalassemia analyzed 17 hemolysates containing 14 different mutant hemoglobins by four electrophoretic methods: (1) cellulose acetate in alkaline buffers, (2)...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors:

    更新日期:1978-11-01 00:00:00

  • Heterochromatic gene repression of the retinoic acid pathway in acute myeloid leukemia.

    abstract::Alteration of lineage-specific transcriptional programs for hematopoiesis causes differentiation block and promotes leukemia development. Here, we show that AML1/ETO, the most common translocation fusion product in acute myeloid leukemia (AML), counteracts the activity of retinoic acid (RA), a transcriptional regulato...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2006-09-045781

    authors: Fazi F,Zardo G,Gelmetti V,Travaglini L,Ciolfi A,Di Croce L,Rosa A,Bozzoni I,Grignani F,Lo-Coco F,Pelicci PG,Nervi C

    更新日期:2007-05-15 00:00:00

  • Platelet von Willebrand's antigen II: active release by aggregating agents and a marker of platelet release reaction in vivo.

    abstract::von Willebrand's antigen II (vW AgII), a plasma and platelet antigen immunologically and biochemically distinct from factor-VIII-related antigen (VIIIR:Ag), is decreased in von Willebrand's disease. vW AgII is released from platelets during aggregation and clotting. The release of platelet vW AgII was studied in washe...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Scott JP,Montgomery RR

    更新日期:1981-12-01 00:00:00

  • The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosis.

    abstract::Lymphomas were studied in kindreds with autoimmune lymphoproliferative syndrome (ALPS; Canale-Smith syndrome), a disorder of lymphocyte homeostasis usually associated with germline Fas mutations. Fas (CD95/APO-1) is a cell surface receptor that initiates programmed cell death, or apoptosis, of activated lymphocytes. L...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.1.194

    authors: Straus SE,Jaffe ES,Puck JM,Dale JK,Elkon KB,Rösen-Wolff A,Peters AM,Sneller MC,Hallahan CW,Wang J,Fischer RE,Jackson CE,Lin AY,Bäumler C,Siegert E,Marx A,Vaishnaw AK,Grodzicky T,Fleisher TA,Lenardo MJ

    更新日期:2001-07-01 00:00:00

  • alpha-Actinin and vinculin in normal and thrombasthenic platelets.

    abstract::Recently, the contractile protein alpha-actinin was identified in normal human platelets by its antigenic cross-reaction with a monospecific antibody to purified muscle alpha-actinin. In this study, we extend that preliminary identification of platelet alpha-actinin. Amino acid analysis, one-dimensional peptide maps, ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Langer BG,Gonnella PA,Nachmias VT

    更新日期:1984-03-01 00:00:00

  • Thalidomide and its analogs overcome drug resistance of human multiple myeloma cells to conventional therapy.

    abstract::Although thalidomide (Thal) was initially used to treat multiple myeloma (MM) because of its known antiangiogenic effects, the mechanism of its anti-MM activity is unclear. These studies demonstrate clinical activity of Thal against MM that is refractory to conventional therapy and delineate mechanisms of anti-tumor a...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:

    authors: Hideshima T,Chauhan D,Shima Y,Raje N,Davies FE,Tai YT,Treon SP,Lin B,Schlossman RL,Richardson P,Muller G,Stirling DI,Anderson KC

    更新日期:2000-11-01 00:00:00

  • It takes a village.

    abstract::In this issue of Blood, Bhatia et al demonstrate the critical importance of an adherence to oral chemotherapy regimens in attaining cure for children with acute lymphoblastic leukemia (ALL) and identify race-specific determinants of adherence. ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2014-05-576900

    authors: Winick N

    更新日期:2014-10-09 00:00:00

  • Membrane-bound serine protease matriptase-2 (Tmprss6) is an essential regulator of iron homeostasis.

    abstract::Proteolytic events at the cell surface are essential in the regulation of signal transduction pathways. During the past years, the family of type II transmembrane serine proteases (TTSPs) has acquired an increasing relevance because of their privileged localization at the cell surface, although our current understandi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-04-149773

    authors: Folgueras AR,de Lara FM,Pendás AM,Garabaya C,Rodríguez F,Astudillo A,Bernal T,Cabanillas R,López-Otín C,Velasco G

    更新日期:2008-09-15 00:00:00

  • Red cell rheology in stomatocyte-echinocyte transformation: roles of cell geometry and cell shape.

    abstract::The influence of the shape of the red blood cell during stomatocyte-echinocyte transformation on its deformability was studied by microsieving through pores with diameters of 2.6, 4.5, and 6.9 micron. A stomatocytic transformation was produced by chlorpromazine (0.02, 0.1, and 0.5 mmol/L) and an echinocytic transforma...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Reinhart WH,Chien S

    更新日期:1986-04-01 00:00:00

  • Subunit structure of the erythropoietin receptor analyzed by 125I-Epo cross-linking in cells expressing wild-type or mutant receptors.

    abstract::To analyze the structure of the murine erythropoietin receptor (EpoR), wild-type or mutant EpoR cDNAs were expressed in cell lines, and the proteins that cross-linked with 125I-labeled erythropoietin (Epo) were analyzed by immunoprecipitation using an antibody against the intracellular region of the cloned EpoR. COS-7...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Miura O,Ihle JN

    更新日期:1993-04-01 00:00:00

  • Identification of talin head domain as an immunodominant epitope of the antiplatelet antibody response in patients with HIV-1-associated thrombocytopenia.

    abstract::HIV-1-associated thrombocytopenia (HIV-1-ITP) is a common complication of HIV-1 infection, frequently caused by increased peripheral platelet destruction mediated by antiplatelet antibodies (Abs) and/or platelet-bound immune complexes. Little is known about the specificity of the antiplatelet Abs at a molecular level....

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-01-0386

    authors: Koefoed K,Ditzel HJ

    更新日期:2004-12-15 00:00:00

  • A 2.7-kb portion of the 5' flanking region of the murine glycoprotein alphaIIb gene is transcriptionally active in primitive hematopoietic progenitor cells.

    abstract::The continuous generation of mature blood cells from primitive multipotent progenitor cells requires a highly complex series of cellular events that are still largely unknown. To examine the molecular events associated with the commitment of these hematopoietic progenitor cells to the megakaryocytic lineage, the alpha...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Tropel P,Roullot V,Vernet M,Poujol C,Pointu H,Nurden P,Marguerie G,Tronik-Le Roux D

    更新日期:1997-10-15 00:00:00

  • Eosinophils contribute to innate antiviral immunity and promote clearance of respiratory syncytial virus.

    abstract::Eosinophils are recruited to the lungs in response to respiratory syncytial virus (RSV) infection; however, their role in promoting antiviral host defense remains unclear. Here, we demonstrate that eosinophils express TLRs that recognize viral nucleic acids, are activated and degranulate after single-stranded RNA (ssR...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-01-071340

    authors: Phipps S,Lam CE,Mahalingam S,Newhouse M,Ramirez R,Rosenberg HF,Foster PS,Matthaei KI

    更新日期:2007-09-01 00:00:00

  • New MLLT10 gene recombinations in pediatric T-acute lymphoblastic leukemia.

    abstract::The MLLT10 gene, located at 10p13, is a known partner of MLL and PICALM in specific leukemic fusions generated from recurrent 11q23 and 11q14 chromosome translocations. Deep sequencing recently identified NAP1L1/12q21 as another MLLT10 partner in T-cell acute lymphoblastic leukemia (T-ALL). In pediatric T-ALL, we have...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2013-02-487256

    authors: Brandimarte L,Pierini V,Di Giacomo D,Borga C,Nozza F,Gorello P,Giordan M,Cazzaniga G,Te Kronnie G,La Starza R,Mecucci C

    更新日期:2013-06-20 00:00:00

  • Elevated serum concentrations of hepatocyte growth factor in patients with multiple myeloma. The Nordic Myeloma Study Group.

    abstract::Serum from 398 myeloma patients at diagnosis and serial samples from 29 patients were analysed for hepatocyte growth factor (HGF). HGF was elevated at diagnosis in 43% of myeloma patients compared with healthy controls (median 1.00 ng/mL and 0.44 ng/mL, respectively; P < .00001). In the group with elevated HGF levels ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Seidel C,Børset M,Turesson I,Abildgaard N,Sundan A,Waage A

    更新日期:1998-02-01 00:00:00

  • Gamma (immune) interferon production by leukocytes from a patient with a TG cell proliferative disease.

    abstract::We report a patient with a disease characterized by proliferation of T cells with Fc receptors for IgG (TG). However, unlike lymphoid cells from normal individuals or from patients with other lymphoid malignancies, the patient's lymphocytes spontaneously produced gamma interferon (IFN-gamma) in vitro. The peripheral l...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Hooks JJ,Haynes BF,Detrick-Hooks B,Diehl LF,Gerrard TL,Fauci AS

    更新日期:1982-01-01 00:00:00