Turnover of Functional Basic Fibroblast Growth Factor Receptors on the Surface of BHK and NIH 3T3 Cells

被引:28
作者
Moscatelli, David [1 ]
Devesly, Pierre
机构
[1] NYU Med Ctr, Dept Cell Biol, 550 First Ave, New York, NY 10016 USA
基金
美国国家卫生研究院;
关键词
Receptor synthesis; receptor down-regulation; receptor degradation;
D O I
10.3109/08977199009037499
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The recovery of functional cell-surface bFGF receptors after trypsin treatment was studied in BHK cells and NIH 3T3 cells. Restoration of functional bFGF receptors occurred at an approximately linear rate with 50% of the high-affinity binding capacity restored after 4 hr. Restoration of functional receptors required protein synthesis but not RNA synthesis. Upon exposure of BHK cells to bFGF, cell-surface receptors were rapidly lost, with only 25% remaining after 1 hr. When the bFGF was removed, down-regulated BHK and NIH 3T3 cells recovered cell-surface receptors at about the same rate observed in trypsin-treated cells. The recovery of receptors after down-regulation was inhibited by protein synthesis inhibitors. Addition of the protein synthesis inhibitor cycloheximide to unperturbed cultures of BHK or NIH 3T3 cells resulted in a time-dependent loss of cell-surface bFGF receptors, demonstrating that the receptors turn over constantly in the absence of ligand. These results suggest that bFGF receptors do not recycle and must be continuously synthesized.
引用
收藏
页码:25 / 33
页数:10
相关论文
共 42 条
[1]   DOWN-REGULATION OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR IN KB CELLS IS DUE TO RECEPTOR INTERNALIZATION AND SUBSEQUENT DEGRADATION IN LYSOSOMES [J].
BEGUINOT, L ;
LYALL, RM ;
WILLINGHAM, MC ;
PASTAN, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (08) :2384-2388
[2]   RECYCLING RECEPTORS - THE ROUND-TRIP ITINERARY OF MIGRANT MEMBRANE-PROTEINS [J].
BROWN, MS ;
ANDERSON, RGW ;
GOLDSTEIN, JL .
CELL, 1983, 32 (03) :663-667
[3]   I125 LABELED HUMAN EPIDERMAL GROWTH-FACTOR - BINDING, INTERNALIZATION, AND DEGRADATION IN HUMAN FIBROBLASTS [J].
CARPENTER, G ;
COHEN, S .
JOURNAL OF CELL BIOLOGY, 1976, 71 (01) :159-171
[4]  
CARPENTER G, 1987, ANNU REV BIOCHEM, V56, P881, DOI 10.1146/annurev.bi.56.070187.004313
[5]   GROWTH-FACTOR CONTROL OF SKELETAL-MUSCLE DIFFERENTIATION - COMMITMENT TO TERMINAL DIFFERENTIATION OCCURS IN G1 PHASE AND IS REPRESSED BY FIBROBLAST GROWTH-FACTOR [J].
CLEGG, CH ;
LINKHART, TA ;
OLWIN, BB ;
HAUSCHKA, SD .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :949-956
[6]  
DANIEL TO, 1987, J BIOL CHEM, V262, P9778
[7]  
DUPREZ V, 1986, J BIOL CHEM, V261, P5450
[8]  
FEIGE JJ, 1988, J BIOL CHEM, V263, P14023
[9]  
GILLESPIE LL, 1989, DEVELOPMENT, V106, P203
[10]   EFFECT OF FIBROBLAST GROWTH-FACTOR AND LIPOPROTEINS ON THE PROLIFERATION OF ENDOTHELIAL-CELLS DERIVED FROM BOVINE ADRENAL-CORTEX, BRAIN CORTEX, AND CORPUS-LUTEUM CAPILLARIES [J].
GOSPODAROWICZ, D ;
MASSOGLIA, S ;
CHENG, J ;
FUJII, DK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 127 (01) :121-136