ALCAM (CD166): its role in hematopoietic and endothelial development.

Abstract:

:A critical role for the endothelium of yolk sac and dorsal aorta has been shown in embryonic hematopoiesis. A stromal cell line derived from yolk sac, YSCL-72, has been chosen to search for a novel molecule associated with embryonic hematopoiesis. Analysis between YSCL-72 and an adult aorta-derived endothelial cell line, EOMA, demonstrated that activated leukocyte cell adhesion molecule (ALCAM, or CD166) was specifically expressed in YSCL-72 but not in EOMA. Immunohistochemical study showed that ALCAM was expressed in the endothelium of yolk sac and dorsal aorta but not in adult aorta. ALCAM-transfected EOMA cells supported development of hematopoietic progenitor cells compared with vector-transfected EOMA cells, suggesting that ALCAM appeared to be crucial for hematopoiesis. In addition, ALCAM was found to be involved in capillary tube formation and hemangioblast differentiation. Taken together with these findings, ALCAM is highly associated not only with embryonic hematopoiesis but also vasculoangiogenesis.

journal_name

Blood

journal_title

Blood

authors

Ohneda O,Ohneda K,Arai F,Lee J,Miyamoto T,Fukushima Y,Dowbenko D,Lasky LA,Suda T

doi

10.1182/blood.v98.7.2134

subject

Has Abstract

pub_date

2001-10-01 00:00:00

pages

2134-42

issue

7

eissn

0006-4971

issn

1528-0020

journal_volume

98

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Modification of hemoglobin by ninhydrin.

    abstract::The Strecker degradation reaction was evaluated as a means of modifying hemoglobin in vitro, utilizing ninhydrin as a model compound. Ninhydrin led to modification of hemoglobin (when incubated with hemoglobin or red cells) at physiologic temperature and pH. Isoelectric focusing documented the formation of new hemoglo...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kokkini G,Stevens VJ,Peterson CM,Cerami A

    更新日期:1980-10-01 00:00:00

  • High-level secretion of tumor necrosis factor-alpha contributes to hematopoietic failure in hairy cell leukemia.

    abstract::Hairy cell leukemia (HCL) is frequently associated with severe pancytopenia. The authors detected high levels of tumor necrosis factor (TNF)-alpha in the bone marrow serum of patients with HCL and found anti-TNF-alpha neutralizing monoclonal antibodies (MoAbs) to be able to enhance hematopoiesis of HCL patients in in ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Lindemann A,Ludwig WD,Oster W,Mertelsmann R,Herrmann F

    更新日期:1989-03-01 00:00:00

  • Soluble CD22 as a tumor marker for hairy cell leukemia.

    abstract::CD22 is an important immunotherapeutic target on B-cell malignancies, particularly hairy cell leukemia (HCL), but its soluble extracellular domain, sCD22, has not yet been reported in the blood. By immunoaffinity and enzyme-linked immunosorbent assay techniques using anti-CD22 monoclonal antibodies, we identified the ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-01-131987

    authors: Matsushita K,Margulies I,Onda M,Nagata S,Stetler-Stevenson M,Kreitman RJ

    更新日期:2008-09-15 00:00:00

  • Hematopoietic progenitors and interleukin-3-dependent cell lines synthesize histamine in response to calcium ionophore.

    abstract::The calcium ionophore A23187 promotes histamine synthesis in murine bone marrow cells by increasing the expression of mRNA encoding histidine decarboxylase (HDC), the histamine-forming enzyme. The cells responsible for this biological activity copurify with hematopoietic progenitors in terms of density, light scatter ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Dy M,Arnould A,Lemoine FM,Machavoine F,Ziltener H,Schneider E

    更新日期:1996-04-15 00:00:00

  • Thrombotic thrombocytopenic purpura and pregnancy: presentation, management, and subsequent pregnancy outcomes.

    abstract::Pregnancy can precipitate thrombotic thrombocytopenic purpura (TTP). We present a prospective study of TTP cases from the United Kingdom Thrombotic Thrombocytopenic Purpura (UK TTP) Registry with clinical and laboratory data from the largest cohort of pregnancy-associated TTP and describe management through pregnancy,...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-02-553131

    authors: Scully M,Thomas M,Underwood M,Watson H,Langley K,Camilleri RS,Clark A,Creagh D,Rayment R,Mcdonald V,Roy A,Evans G,McGuckin S,Ni Ainle F,Maclean R,Lester W,Nash M,Scott R,O Brien P,collaborators of the UK TTP Registr

    更新日期:2014-07-10 00:00:00

  • Local and systemic induction of CD4+CD25+ regulatory T-cell population by non-Hodgkin lymphoma.

    abstract::Regulatory T (Treg) cells contribute to immune evasion by malignancies. To investigate their importance in non-Hodgkin lymphoma (NHL), we enumerated Treg cells in peripheral blood mononuclear cells (PBMCs) and involved tissues from 30 patients. CD25(+)FoxP3(+)CD127(low)CD4(+) Treg cells were increased markedly in PBMC...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-08-105395

    authors: Mittal S,Marshall NA,Duncan L,Culligan DJ,Barker RN,Vickers MA

    更新日期:2008-06-01 00:00:00

  • B-cell antigen receptor signaling enhances chronic lymphocytic leukemia cell migration and survival: specific targeting with a novel spleen tyrosine kinase inhibitor, R406.

    abstract::Antigenic stimulation through the B-cell antigen receptor (BCR) is considered to promote the expansion of chronic lymphocytic leukemia (CLL) B cells. The spleen tyrosine kinase (Syk), a key component of BCR signaling, can be blocked by R406, a small-molecule Syk inhibitor, that displayed activity in CLL patients in a ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-03-212837

    authors: Quiroga MP,Balakrishnan K,Kurtova AV,Sivina M,Keating MJ,Wierda WG,Gandhi V,Burger JA

    更新日期:2009-07-30 00:00:00

  • Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

    abstract::The congenital sideroblastic anemias (CSAs) are relatively uncommon diseases characterized by defects in mitochondrial heme synthesis, iron-sulfur (Fe-S) cluster biogenesis, or protein synthesis. Here we demonstrate that mutations in HSPA9, a mitochondrial HSP70 homolog located in the chromosome 5q deletion syndrome 5...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2015-09-659854

    authors: Schmitz-Abe K,Ciesielski SJ,Schmidt PJ,Campagna DR,Rahimov F,Schilke BA,Cuijpers M,Rieneck K,Lausen B,Linenberger ML,Sendamarai AK,Guo C,Hofmann I,Newburger PE,Matthews D,Shimamura A,Snijders PJ,Towne MC,Niemeyer CM,

    更新日期:2015-12-17 00:00:00

  • Attachment of the PSGL-1 cytoplasmic domain to the actin cytoskeleton is essential for leukocyte rolling on P-selectin.

    abstract::P-selectin glycoprotein ligand-1 (PSGL-1) serves as the leukocyte ligand for P-selectin, and many of the structural features of its ectodomain required for interactions with P-selectin have been uncovered. In contrast, the function of the highly conserved PSGL-1 cytoplasmic domain has not been explored. Stable transfe...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v99.12.4494

    authors: Snapp KR,Heitzig CE,Kansas GS

    更新日期:2002-06-15 00:00:00

  • Separation of erythroid progenitor cells in mouse bone marrow by isokinetic-gradient sedimentation.

    abstract::Isokinetic-gradient sedimentation employing a shallow linear gradient of Ficoll in tissue culture medium was used to isolate erythroid progenitor cells (CFU-e) from mouse bone marrow. Following gradient sedimentation, 34% of the total nucleated cells and 48% of the CFU-e applied to the gradient were recovered, and thr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Misiti J,Spivak JL

    更新日期:1979-07-01 00:00:00

  • The biology and clinical impact of genetic lesions in myeloid malignancies.

    abstract::A longstanding endeavor to define the genetic lesions that drive myeloid malignances has stimulated a period of remarkable discovery. Enabled by technological advances that have sharply decreased the cost of DNA sequencing, the full compendium of common, recurrent somatic mutations in the coding genome of myeloid mali...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2013-06-460295

    authors: Lindsley RC,Ebert BL

    更新日期:2013-11-28 00:00:00

  • A genome-wide association analysis of serum iron concentrations.

    abstract::To investigate genetic variants that affect iron concentrations in persons not affected by overt genetic disorders of iron metabolism, a genome-wide association study was conducted in the InCHIANTI Study (N = 1206) and the Baltimore Longitudinal Study of Aging (N = 713). The top 2 single-nucleotide polymorphisms were ...

    journal_title:Blood

    pub_type: 杂志文章,meta分析

    doi:10.1182/blood-2009-07-232496

    authors: Tanaka T,Roy CN,Yao W,Matteini A,Semba RD,Arking D,Walston JD,Fried LP,Singleton A,Guralnik J,Abecasis GR,Bandinelli S,Longo DL,Ferrucci L

    更新日期:2010-01-07 00:00:00

  • Clinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling.

    abstract::Microarray gene expression profiling studies have demonstrated immune response gene signatures that appear predictive of outcome in follicular lymphoma (FL). However, measurement of these marker genes in routine practice remains difficult. We have therefore investigated the immune response in FL using real-time polyme...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2007-10-115915

    authors: Byers RJ,Sakhinia E,Joseph P,Glennie C,Hoyland JA,Menasce LP,Radford JA,Illidge T

    更新日期:2008-05-01 00:00:00

  • Controlled trial of filgrastim for acceleration of neutrophil recovery after allogeneic blood stem cell transplantation from human leukocyte antigen-matched related donors.

    abstract::The rapid recovery of hematopoiesis after allogeneic blood stem cell transplantation has been attributed to the quality and quantity of hematopoietic progenitors in the blood stem cell grafts from filgrastim-stimulated donors. To determine whether further stimulation with filgrastim after transplantation would affect ...

    journal_title:Blood

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1182/blood.v97.11.3405

    authors: Przepiorka D,Smith TL,Folloder J,Anderlini P,Chan KW,Körbling M,Lichtiger B,Norfleet F,Champlin R

    更新日期:2001-06-01 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

  • Thrombin induces the expression of oncostatin M via AP-1 activation in human macrophages: a link between coagulation and inflammation.

    abstract::Macrophages as inflammatory cells are involved in the pathogenesis of atherosclerosis that today is recognized as an inflammatory disease. Activation of coagulation leads to the late complication of atherosclerosis, namely atherothrombosis with its clinical manifestations stroke, unstable angina, myocardial infarction...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-01-200915

    authors: Kastl SP,Speidl WS,Katsaros KM,Kaun C,Rega G,Assadian A,Hagmueller GW,Hoeth M,de Martin R,Ma Y,Maurer G,Huber K,Wojta J

    更新日期:2009-09-24 00:00:00

  • In vivo inhibition by a site-specific catalytic RNA subunit of RNase P designed against the BCR-ABL oncogenic products: a novel approach for cancer treatment.

    abstract::One major obstacle to the effective treatment of cancer is to distinguish between tumor cells and normal cells. The chimeric molecules created by cancer-associated chromosomal abnormalities are ideal therapeutic targets because they are unique to the disease. We describe the use of a novel approach based on the cataly...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Cobaleda C,Sánchez-García I

    更新日期:2000-02-01 00:00:00

  • The repopulation potential of fetal liver hematopoietic stem cells in mice exceeds that of their liver adult bone marrow counterparts.

    abstract::Varying, limiting numbers of unseparated or purified cells (Ly-5.1), either from 14.5-day-old fetal liver (FL) or from adult bone marrow (BM) were coinjected with 10(5) unseparated BM cells (Ly-5.2) into lethally irradiated adult C57B1/6 recipients (Ly-5.2). The kinetics of donor cell repopulation of the lymphoid and ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Rebel VI,Miller CL,Eaves CJ,Lansdorp PM

    更新日期:1996-04-15 00:00:00

  • Hematologic engraftment and immune reconstitution posttransplantation with anti-B1 purged autologous bone marrow.

    abstract::Hematologic engraftment and immune reconstitution were examined in patients who received cyclophosphamide and total body irradiation therapy followed by infusion of autologous bone marrow purged with anti-B1 monoclonal antibody (MoAb) and complement as therapy for non-Hodgkin's lymphoma. Hematologic engraftment was pr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Anderson KC,Ritz J,Takvorian T,Coral F,Daley H,Gorgone BC,Freedman AS,Canellos GP,Schlossman SF,Nadler LM

    更新日期:1987-02-01 00:00:00

  • Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes.

    abstract::A cohort of MDS patients was examined for mutations affecting 4 splice genes (SF3B1, SRSF2, ZRSR2, and U2AF35) and evaluated in the context of clinical and molecular markers. Splice gene mutations were detected in 95 of 221 patients. These mutations were mutually exclusive and less likely to occur in patients with com...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-12-400994

    authors: Damm F,Kosmider O,Gelsi-Boyer V,Renneville A,Carbuccia N,Hidalgo-Curtis C,Della Valle V,Couronné L,Scourzic L,Chesnais V,Guerci-Bresler A,Slama B,Beyne-Rauzy O,Schmidt-Tanguy A,Stamatoullas-Bastard A,Dreyfus F,Prébet T,

    更新日期:2012-04-05 00:00:00

  • Expression, localization, and regulation of NOS in human mast cell lines: effects on leukotriene production.

    abstract::Nitric oxide (NO) is a potent radical produced by nitric oxide synthase (NOS) and has pleiotrophic activities in health and disease. As mast cells (MCs) play a central role in both homeostasis and pathology, we investigated NOS expression and NO production in human MC populations. Endothelial NOS (eNOS) was ubiquitous...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-08-2990

    authors: Gilchrist M,McCauley SD,Befus AD

    更新日期:2004-07-15 00:00:00

  • End-linked homodimers in fibrinogen Osaka VI with a B beta-chain extension lead to fragile clot structure.

    abstract::The authors have identified a 12-residue carboxyl-terminal extension of Lys-Ser-Pro-Met-Arg-Arg-Phe-Leu-Leu-Phe-Cys-Met in a dysfibrinogen derived from a woman heterozygotic for this abnormality and associated with severe bleeding. This extension is due to a T-to-A mutation that creates AAG encoding Lys at the stop (T...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Sugo T,Nakamikawa C,Yoshida N,Niwa K,Sameshima M,Mimuro J,Weisel JW,Nagita A,Matsuda M

    更新日期:2000-12-01 00:00:00

  • Proteolytic inactivation of ADAMTS13 by thrombin and plasmin.

    abstract::The multimeric size and the function of circulating von Willebrand factor are modulated via its proteolytic cleavage by the plasma metalloproteinase, ADAMTS13. It is unclear how ADAMTS13 activity is regulated within the vascular system. In the absence of a regulatory mechanism, ADAMTS13 activity might compromise plate...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-03-1101

    authors: Crawley JT,Lam JK,Rance JB,Mollica LR,O'Donnell JS,Lane DA

    更新日期:2005-02-01 00:00:00

  • Large granular lymphocytes in human peripheral blood: ultrastructural and cytochemical characterization of the granules.

    abstract::Large granular lymphocytes (LGL) are defined as nonadherent mononuclear cells with cytoplasmic azurophilic granules, avid receptors for the Fc portion of IgG, and cytotoxic functions (NK or ADCC activities). In the present study, the granules of LGL isolated from human peripheral blood have been analyzed by enzyme cyt...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Grossi CE,Cadoni A,Zicca A,Leprini A,Ferrarini M

    更新日期:1982-02-01 00:00:00

  • Improved hemostasis with superactive analogs of factor VIIa in a mouse model of hemophilia A.

    abstract::It is currently debated whether the mechanism of action of therapeutic doses of recombinant factor VIIa (rFVIIa, Novo-Seven) relies on the tissue factor (TF)-independent activity of the enzyme. The present study was conducted to investigate the in vivo hemostatic effects of rFVIIa and 3 analogs thereof with superior i...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-05-1369

    authors: Tranholm M,Kristensen K,Kristensen AT,Pyke C,Røjkjaer R,Persson E

    更新日期:2003-11-15 00:00:00

  • Multiple myeloma.

    abstract::Multiple myeloma is a clonal plasma cell malignancy that accounts for slightly more than 10% of all hematologic cancers. In this paper, we present a historically focused review of the disease, from the description of the first case in 1844 to the present. The evolution of drug therapy and stem-cell transplantation for...

    journal_title:Blood

    pub_type: 历史文章,杂志文章,评审

    doi:10.1182/blood-2007-10-078022

    authors: Kyle RA,Rajkumar SV

    更新日期:2008-03-15 00:00:00

  • How I diagnose and treat venous thromboembolism in sickle cell disease.

    abstract::The incidence of venous thromboembolism (VTE) in adult patients with sickle cell disease (SCD) is high. However, overlapping features between the clinical presentation of VTE and SCD complications and a low index of suspicion for thrombosis can influence patient management decisions. VTE in SCD can therefore present m...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2018-03-822593

    authors: Shet AS,Wun T

    更新日期:2018-10-25 00:00:00

  • BVL-1-like VL30 promoter sustains long-term expression in erythroid progenitor cells.

    abstract::Congenital blood disorders are common and yet clinically challenging globin disorders. Gene therapy continues to serve as a potential therapeutic method to treat these disorders. While tremendous advances have been made in vivo, gene delivery protocols and vector prototypes still require optimization. Alternative cis-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-07-2105

    authors: Staplin WR,Knezetic JA

    更新日期:2003-03-01 00:00:00

  • Mouse fetal liver cells lack functional amphotropic retroviral receptors.

    abstract::We have been transducing mouse hematopoietic cells with the human MDR1 (MDR) gene in retroviral vectors to determine the optimal conditions for retroviral gene transfer as a model system for potential human gene therapy. In these studies, we have demonstrated transduction and expression of the human MDR gene using eco...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Richardson C,Ward M,Podda S,Bank A

    更新日期:1994-07-15 00:00:00

  • DNMT3A and TET2 dominate clonal hematopoiesis and demonstrate benign phenotypes and different genetic predispositions.

    abstract::Age-associated clonal hematopoiesis caused by acquired mutations in myeloid cancer-associated genes is highly prevalent in the normal population. Its etiology, biological impact on hematopoiesis, and oncogenic risk is poorly defined at this time. To gain insight into this phenomenon, we analyzed a cohort of 2530 relat...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2017-04-777029

    authors: Buscarlet M,Provost S,Zada YF,Barhdadi A,Bourgoin V,Lépine G,Mollica L,Szuber N,Dubé MP,Busque L

    更新日期:2017-08-10 00:00:00