Fibroblast Growth Factors Are Translocated to the Nucleus of Human Endothelial Cells in a Microtubule- and Lysosome-Independent Pathway
Identifieur interne : 002546 ( Main/Exploration ); précédent : 002545; suivant : 002547Fibroblast Growth Factors Are Translocated to the Nucleus of Human Endothelial Cells in a Microtubule- and Lysosome-Independent Pathway
Auteurs : Guo-Fu Hu ; Hyun-Ju Kim ; Chi-Jie Xu ; James F. RiordanSource :
- Biochemical and Biophysical Research Communications [ 0006-291X ] ; 2000.
English descriptors
- Teeft :
- Acad, Afgf, Angiogenic, Angiogenic factors, Angiogenic proteins, Angiogenin, Bfgf, Biochem, Biol, Biophysical research communications, Broblast, Broblast growth factor, Broblast growth factors, Cell biol, Cell nucleus, Cell proliferation, Chloroquine, Cytosol, Cytosolic, Cytosolic accumulation, Estradiol, Fgfs, Fusion protein, Growth factor, Growth factors, Human umbilical artery, Human umbilical vein, Huve, Huve cells, Leupeptin, Lysosomal, Lysosomal inhibitors, Lysosomal processing, Microtubule, Microtubule network, Natl, Nuclear translocation, Plasma membrane, Proc, Receptor, Subcellular, Subcellular distribution, Subcellular fraction, Translocation, Umbilical.
Abstract
Abstract: Exogenous acidic and basic fibroblast growth factors undergo rapid nuclear translocation in human umbilical vein endothelial cells. When nuclear translocation reaches saturation, more than 70% of the internalized growth factors are in the nuclear fraction. Lysosomal inhibitors, such as leupeptin and chloroquine, and microtubule inhibitors including colchicine and 2-methoxyl-β-estradiol neither increase nor decrease nuclear translocation. The results suggest that nuclear translocation of fibroblast growth factors does not require cytosolic accumulation or lysosomal processing and that the transportation of exogenous growth factors across the cytoplasm is independent of microtubules.
Url:
DOI: 10.1006/bbrc.2000.2978
Affiliations:
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Le document en format XML
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<term>Afgf</term>
<term>Angiogenic</term>
<term>Angiogenic factors</term>
<term>Angiogenic proteins</term>
<term>Angiogenin</term>
<term>Bfgf</term>
<term>Biochem</term>
<term>Biol</term>
<term>Biophysical research communications</term>
<term>Broblast</term>
<term>Broblast growth factor</term>
<term>Broblast growth factors</term>
<term>Cell biol</term>
<term>Cell nucleus</term>
<term>Cell proliferation</term>
<term>Chloroquine</term>
<term>Cytosol</term>
<term>Cytosolic</term>
<term>Cytosolic accumulation</term>
<term>Estradiol</term>
<term>Fgfs</term>
<term>Fusion protein</term>
<term>Growth factor</term>
<term>Growth factors</term>
<term>Human umbilical artery</term>
<term>Human umbilical vein</term>
<term>Huve</term>
<term>Huve cells</term>
<term>Leupeptin</term>
<term>Lysosomal</term>
<term>Lysosomal inhibitors</term>
<term>Lysosomal processing</term>
<term>Microtubule</term>
<term>Microtubule network</term>
<term>Natl</term>
<term>Nuclear translocation</term>
<term>Plasma membrane</term>
<term>Proc</term>
<term>Receptor</term>
<term>Subcellular</term>
<term>Subcellular distribution</term>
<term>Subcellular fraction</term>
<term>Translocation</term>
<term>Umbilical</term>
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<front><div type="abstract" xml:lang="en">Abstract: Exogenous acidic and basic fibroblast growth factors undergo rapid nuclear translocation in human umbilical vein endothelial cells. When nuclear translocation reaches saturation, more than 70% of the internalized growth factors are in the nuclear fraction. Lysosomal inhibitors, such as leupeptin and chloroquine, and microtubule inhibitors including colchicine and 2-methoxyl-β-estradiol neither increase nor decrease nuclear translocation. The results suggest that nuclear translocation of fibroblast growth factors does not require cytosolic accumulation or lysosomal processing and that the transportation of exogenous growth factors across the cytoplasm is independent of microtubules.</div>
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<tree><noCountry><name sortKey="Hu, Guo Fu" sort="Hu, Guo Fu" uniqKey="Hu G" first="Guo-Fu" last="Hu">Guo-Fu Hu</name>
<name sortKey="Kim, Hyun Ju" sort="Kim, Hyun Ju" uniqKey="Kim H" first="Hyun-Ju" last="Kim">Hyun-Ju Kim</name>
<name sortKey="Riordan, James F" sort="Riordan, James F" uniqKey="Riordan J" first="James F." last="Riordan">James F. Riordan</name>
<name sortKey="Xu, Chi Jie" sort="Xu, Chi Jie" uniqKey="Xu C" first="Chi-Jie" last="Xu">Chi-Jie Xu</name>
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