Document Detail


Cell cycle-dependent nuclear localization of exogenously added fibroblast growth factor-1 in BALB/c 3T3 and human vascular endothelial cells.
MedLine Citation:
PMID:  7982474     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Previous studies have shown that the presence of a functional nuclear targeting sequence in the primary structure of fibroblast growth factor (FGF)-1 correlates with its activity as a mitogen, but not with its potential for inducing receptor tyrosine phosphorylation, suggesting the presence of a yet undefined function of FGF-1 as a nuclear protein. In the present study we have investigated the cytosolic and nuclear localization of exogenously added FGF-1. FGF-1-specific monoclonal antibodies were raised. By an extensive screening, highly specific antibody clones were isolated. For both BALB/c 3T3 and human umbilical vein endothelial (HUVE) cells, immunofluorescence studies performed with those clones delineated that during G1 stage of cell cycle, FGF-1 transits from cytosol to nucleus. This was followed by a shift to the perinuclear and juxtanuclear region just prior to the onset of S-phase in BALB/c 3T3 cells. Confocal microscopical examinations confirmed that the nuclear staining resides throughout the nuclear matrix with some enrichment at the envelope boundary and in the nucleoli. Immunoblot analysis of the fractionated BALB/c 3T3 cells that had been induced to proliferate by serum and pulsed with exogenous FGF-1 at various timings revealed that the incorporation of exogenous FGF-1 into cytosol took place constantly, whereas the nuclear translocation significantly increased after 5 h following stimulation of the quiescent cells. The cytosolic form of FGF-1 is indicated to be present in soluble cytosolic fraction rather than membrane-enveloped compartments, endosomes, by the microinjection of anti FGF-1 antibody to HUVE cells cultured in the presence of FGF-1. The data demonstrate that the exogenously added FGF-1 is constantly endocytosed and fractioned into the cytosol soluble compartment, whereas its nuclear localization is regulated at the nuclear translocation level and takes place preferably at late G1 phase of the cell cycle.
Authors:
T Imamura; S Oka; T Tanahashi; Y Okita
Related Documents :
8526904 - Expression of ptp35, the murine homologue of the protein tyrosine phosphatase-related s...
15020134 - The effect of galectin 1 on 3t3 cell proliferation on chitosan membranes.
6395454 - Rat thymocyte subpopulations: heterogeneity of the fetal calf serum dependent rosette f...
16595654 - Phospholipase d couples survival and migration signals in stress response of human canc...
8906424 - After embryonic day 17, distribution of cells on surface of primary muscle fibres in mo...
23271434 - Reversible and irreversible electroporation of cell suspensions flowing through a local...
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Experimental cell research     Volume:  215     ISSN:  0014-4827     ISO Abbreviation:  Exp. Cell Res.     Publication Date:  1994 Dec 
Date Detail:
Created Date:  1995-01-03     Completed Date:  1995-01-03     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0373226     Medline TA:  Exp Cell Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  363-72     Citation Subset:  IM    
Affiliation:
Cell Biology Laboratory, National Institute of Bioscience and Human Technology, Ibaraki, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
3T3 Cells
Animals
Antibodies, Monoclonal
Cell Cycle
Cell Division
Cell Nucleus / metabolism
Cells, Cultured
Cytosol / metabolism
Endothelium, Vascular / cytology,  metabolism
Fibroblast Growth Factors / immunology,  metabolism*
Fluorescent Antibody Technique
Humans
Mice
Chemical
Reg. No./Substance:
0/Antibodies, Monoclonal; 62031-54-3/Fibroblast Growth Factors

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  N-CAM and N-cadherin expression during in vitro chondrogenesis.
Next Document:  Induction of apoptosis by the anti-tubulin drug colcemid: relationship of mitotic checkpoint control...