Gewählte Publikation:
Ljungberg, MC; Asuni, A; Pearce, J; Dayanandan, R; März, W; Hoffmann, MM; Bertrand, P; Siest, G; Rupniak, HT; Anderton, BH; Huettinger, M; Lovestone, S.
Apolipoprotein E (apoE) uptake and distribution in mammalian cell lines is dependent upon source of apoE and can be monitored in living cells.
Neurosci Lett. 2003; 341(1):69-73
Doi: 10.1016%2FS0304-3940%2803%2900064-8
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- Co-Autor*innen der Med Uni Graz
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März Winfried
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- Abstract:
- As part of investigations of the cellular uptake of apolipoprotein E (apoE) relevant to Alzheimer's disease we have found that different preparations of apoE are handled differently by cells expressing the LDL-receptor. Comparing recombinant, cellular and native apoE, complexed with different preparations of lipid we find that only cellular and native apoE enter a vesicular compartment. Some, but not all of these apoE containing vesicles are lysosomes. In order to further examine the intracellular fate of apoE we demonstrate that apoE-Enhanced green fluorescent protein chimeric protein can be taken up from medium by recipient cells and tracked within these cells for extended periods.
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Animals -
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Apolipoproteins E - metabolism
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COS Cells - metabolism
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Cell Line - metabolism
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Cercopithecus aethiops - metabolism
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Escherichia coli - metabolism
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Humans - metabolism
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Mice - metabolism
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Protein Isoforms - metabolism
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Rabbits - metabolism
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Recombinant Proteins - metabolism
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Tumor Cells, Cultured - metabolism
- Find related publications in this database (Keywords)
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apolipoprotein E
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tau
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beta VLDL
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enhanced green fluorescent protein
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Alzheimer's disease
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uptake
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apolipoprotein