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Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis.

Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Research Abstract Details 

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  • Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Abstract Text:

    wenbo zhangWenbo Zhang,jean-marc navenotJean-Marc Navenot,nicole m frilotNicole M Frilot,nobutaka fujiiNobutaka Fujii,stephen c peiperStephen C Peiper,wenbo zhangWenbo Zhang,jean-marc navenotJean-Marc Navenot,nicole m frilotNicole M Frilot,nobutaka fujiiNobutaka Fujii,stephen c peiperStephen C Peiper,

    CXCR4, the primary receptor for CXCL12, plays a critical role in the development of hematopoietic, vascular, central nervous, and immune systems by mediating directional migration of precursor cells. This mechanism promotes homing of tumor cells to metastatic sites that secrete CXCL12, and CXCR4 expression is a negative prognostic factor in acute myelogenous leukemia (AML). To elucidate mechanisms that regulate CXCR4 signaling, we used a proteomic approach to identify proteins physically associated with CXCR4. Analysis of CXCR4 immune complexes identified nucleophosmin (NPM), which was confirmed by reciprocal coimmunoprecipitation for NPM. Constitutively active CXCR4 variants bound higher levels of NPM than the wild-type receptor, which was reversed by T140, an inverse agonist. NPM binding to CXCR4 localized interactions to the C terminus and cytoplasmic loop (CL)-3, but not CL-1 or CL-2. Alanine scanning mutagenesis demonstrated that positively charged amino acids in CL-3 were critical for NPM binding. Recombinant NPM decreased GTP binding in membrane fractions after activation of CXCR4 by CXCL12. Suppression of NPM expression enhanced chemotactic responses to CXCL12, and, conversely, overexpression of a cytosolic NPM mutant reduced chemotaxis induced by CXCL12. This study provides evidence for a novel role for NPM as a negative regulator of CXCR4 signaling induced by CXCL12 that may be relevant to the biology of AML.

    Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Publishing Authors By Initials

    w zhangW Zhang,jm navenotJM Navenot,nm frilotNM Frilot,n fujiiN Fujii,sc peiperSC Peiper,w zhangW Zhang,jm navenotJM Navenot,nm frilotNM Frilot,n fujiiN Fujii,sc peiperSC Peiper,

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    PUBMED ID PMID:

    MEDLINE DATE:

    Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Molecular pharmacology

    VOLUME: 72

    Page Numbers: 1310-21

    Journal Abbreviation: Mol. Pharmacol.

    ISSN: 0026-895X

    DAY: 22

    MONTH: 08

    YEAR: 2007

    Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Information

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    LANGUAGE: eng

    NlmUniqueID: 35623

    Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis. Information

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    Grant and Affiliation Information for Association of nucleophosmin negatively regulates CXCR4-mediated G protein activation and chemotaxis.

    AFFILIATION: Department of Pathology, Medical College of Georgia, Augusta, GA 30912, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAID

    GRANT: AI41346

    ACRONYM: AI

    MEDLINETA: Mol Pharmacol

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