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Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation.

Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Research Abstract Details 

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  • Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Abstract Text:

    shivani soniShivani Soni,shashi balaShashi Bala,ajay kumarAjay Kumar,manjit hanspalManjit Hanspal,

    Erythroblast macrophage protein (Emp) mediates the attachment of erythroid cells to macrophages and is required for normal differentiation of both cell lineages. In erythroid cells, Emp is believed to be involved in nuclear extrusion, however, its role in macrophage differentiation is unknown. Information on the changes in the expression level and subcellular distribution of Emp in differentiating macrophages is essential for understanding the function of Emp. Macrophages of varying maturity were examined by immunofluorescence microscopy and biochemical methods. Our data show that Emp is expressed in all stages of maturation, but its localization pattern changes dramatically during maturation: in immature macrophages, a substantial fraction of Emp is associated with the nuclear matrix, whereas in more mature cells, Emp is expressed largely at cell surface. Pulse-chase experiments show that nascent Emp migrates intracellularly from the cytoplasm to the plasma membrane more efficiently in mature macrophages than in immature cells. Incubation of erythroid cells with macrophages in culture shows that erythroid cells attach to mature macrophages but not to immature macrophage precursors. Together, our data show that the temporal and spatial expression of Emp correlates with its role in erythroblastic island formation and suggest that Emp may be involved in multiple cellular functions.

    Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Publishing Authors By Initials

    s soniS Soni,s balaS Bala,a kumarA Kumar,m hanspalM Hanspal,

    For similar cells: cellular structures: subcellular fractions research abstracts see: cells: cellular structures: subcellular fractions research

    PUBMED ID PMID:

    MEDLINE DATE: 2007 Jan-Feb

    Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Blood cells, molecules & diseases

    VOLUME: 38

    Page Numbers: 25-31

    Journal Abbreviation: Blood Cells Mol. Dis.

    ISSN: 1079-9796

    DAY: 27

    MONTH: 10

    YEAR: 2006

    Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9509932

    Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Keywords Mesh Terms:

    KEYWORDS: Subcellular Fractions

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation. Information

    Substance Name: erythroblast macrophage protein, mouse

    Registry Number: 0

    Grant and Affiliation Information for Changing pattern of the subcellular distribution of erythroblast macrophage protein (Emp) during macrophage differentiation.

    AFFILIATION: Department of Medicine, Center for Cell Biology, CBR 406, Caritas St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA 02135, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAID

    GRANT: R01 AI050600-05

    ACRONYM: AI

    MEDLINETA: Blood Cells Mol Dis

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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