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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
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.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Apolipoproteins E - metabolism
COS Cells - metabolism
Cell Line - metabolism
Cercopithecus aethiops - metabolism
Escherichia coli - metabolism
Humans - metabolism
Mice - metabolism
Protein Isoforms - metabolism
Rabbits - metabolism
Recombinant Proteins - metabolism
Tumor Cells, Cultured - metabolism

Find related publications in this database (Keywords)
apolipoprotein E
tau
beta VLDL
enhanced green fluorescent protein
Alzheimer's disease
uptake
apolipoprotein
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