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Radboud Repository
Article . 2005
Data sources: Radboud Repository
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Cellular and Molecular Neurobiology
Article . 2005 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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Subcellular Localization and Differentiation-Induced Redistribution of the Protein Tyrosine Phosphatase PTP-BL in Neuroblastoma Cells

Authors: Ham, M. van der; Kemperman, L.; Wijers-Rouw, M.J.P.; Fransen, J.; Hendriks, W.J.A.J.;

Subcellular Localization and Differentiation-Induced Redistribution of the Protein Tyrosine Phosphatase PTP-BL in Neuroblastoma Cells

Abstract

1. In cells of epithelial origin the protein tyrosine phosphatase PTP-BL is predominantly localized at the apical membrane of polarized cells. This large submembranous multidomain PTP is also expressed in cells of neuronal origin. We studied the localization of PTP-BL in mouse neuroblastoma cells utilizing EGFP-tagged versions of the protein. 2. In proliferating Neuro-2a cells, immunofluorescence and immuno-electron microscopy revealed a submembranous FERM domain-dependent localization at cell-cell boundaries for EGFP-PTP-BL. Additionally, significant amounts of EGFP-PTP-BL are located in the cytoplasm as well as in nuclei. Upon serum depletion-induced differentiation of Neuro-2a cells, a partial shift of EGFP-PTP-BL from a cortical localization to cytoskeleton-like F-actin-positive structures is observed. Parallel biochemical studies corroborate this finding and reveal a serum depletion-induced shift of EFGP-PTP-BL from a membrane(-associated) fraction to an NP40-soluble cytoskeletal fraction. 3. Different pools of PTP-BL-containing protein complexes can be discerned in neuronal cells, reflecting distinct molecular microenvironments in which PTP-BL may exert its function.

Related Organizations
Keywords

Cytoplasm, Macromolecular Substances, DCN 2: Functional Neurogenomics, Green Fluorescent Proteins, Protein Tyrosine Phosphatase, Non-Receptor Type 13, N4i 1: Pathogenesis and modulation of inflammation, Culture Media, Serum-Free, Mice, Neuroblastoma, UMCN 5.3: Cellular energy metabolism, Cell Line, Tumor, Animals, NCEBP 2: Evaluation of complex medical interventions, Cells, Cultured, Cytoskeleton, Cell Nucleus, Neurons, Cell Membrane, Cell Differentiation, Actins, Cell Compartmentation, Protein Structure, Tertiary, Actin Cytoskeleton, Protein Transport, N4i 4: Auto-immunity, transplantation and immunotherapy, NCMLS 7: Chemical and physical biology

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
4
Average
Average
Average