• Login
    View Item 
    •   Home
    • The Manchester Institute Cancer Research UK
    • All Paterson Institute for Cancer Research
    • View Item
    •   Home
    • The Manchester Institute Cancer Research UK
    • All Paterson Institute for Cancer Research
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of ChristieCommunitiesTitleAuthorsIssue DateSubmit DateSubjectsThis CollectionTitleAuthorsIssue DateSubmit DateSubjectsProfilesView

    My Account

    LoginRegister

    Local Links

    The Christie WebsiteChristie Library and Knowledge Service

    Statistics

    Display statistics

    Identification of a serpin specifically expressed in multipotent and bipotent hematopoietic progenitor cells and in activated T cells.

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Authors
    Hampson, Ian N
    Hampson, Lynne
    Pinkoski, M
    Cross, M
    Heyworth, Clare M
    Bleackley, R C
    Atkinson, E
    Dexter, T Michael
    Affiliation
    CRC Department of Experimental Haematology, Paterson Institute of Cancer Research, Christie Hospital, Manchester, UK.
    Issue Date
    1997-01-01
    
    Metadata
    Show full item record
    Abstract
    We have identified a gene that has a high level of mRNA expression in undifferentiated, multipotential hematopoietic cells (FDCP-Mix) and that downregulates both transcript and protein, as these cells are induced to differentiate into mature myeloid cells. Sequence analysis of this gene has identified it as a serine protease inhibitor EB22/3 (serpin 2A). Constitutive expression of serpin 2A in FDCP-Mix cells was associated with an increase in the clonogenic potential of the cells and with a delay in the appearance of fully mature cells in cultures undergoing granulocyte macrophage differentiation when compared with control cells. Serpin 2A was also found to be expressed in bone marrow-derived bipotent granulocyte macrophage progenitor cells (GM-colony forming cell [CFC]), but not in erythrocyte progenitor cells from day 15 fetal liver. Expression of serpin 2A also showed a marked up regulation during the activation of cytotoxic suppressor CD8+ T cells, with a clear lag between the appearance of transcript and detection of protein.
    Citation
    Identification of a serpin specifically expressed in multipotent and bipotent hematopoietic progenitor cells and in activated T cells. 1997, 89 (1):108-18 Blood
    Journal
    Blood
    URI
    http://hdl.handle.net/10541/94933
    PubMed ID
    8978283
    Type
    Article
    Language
    en
    ISSN
    0006-4971
    Collections
    All Paterson Institute for Cancer Research

    entitlement

    Related articles

    • A minimal serpin promoter with high activity in haematopoietic progenitors and activated T cells.
    • Authors: Hampson L, Hampson IN, Babichuk CK, Cotter L, Bleackley RC, Dexter TM, Cross MA
    • Issue date: 2001
    • Isolation of MYADM, a novel hematopoietic-associated marker gene expressed in multipotent progenitor cells and up-regulated during myeloid differentiation.
    • Authors: Pettersson M, Dannaeus K, Nilsson K, Jönsson JI
    • Issue date: 2000 Mar
    • IL-4 promotes macrophage development by rapidly stimulating lineage restriction of bipotent granulocyte-macrophage colony-forming cells.
    • Authors: Nicholls SE, Heyworth CM, Dexter TM, Lord JM, Johnson GD, Whetton AD
    • Issue date: 1995 Jul 15
    • Role of members of the Wnt gene family in human hematopoiesis.
    • Authors: Van Den Berg DJ, Sharma AK, Bruno E, Hoffman R
    • Issue date: 1998 Nov 1
    • Transient expression of PU.1 commits multipotent progenitors to a myeloid fate whereas continued expression favors macrophage over granulocyte differentiation.
    • Authors: McIvor Z, Hein S, Fiegler H, Schroeder T, Stocking C, Just U, Cross M
    • Issue date: 2003 Jan
    DSpace software (copyright © 2002 - 2025)  DuraSpace
    Quick Guide | Contact Us
    Open Repository is a service operated by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.