Effects of TSH and cyclic AMP on the human thyroid cells cultured in a chemically defined medium

1977 ◽  
Vol 33 (2) ◽  
pp. 281-282 ◽  
Author(s):  
Y. Kaneko
1981 ◽  
Vol 88 (2) ◽  
pp. 187-NP ◽  
Author(s):  
J. R. BOURKE ◽  
K. L. CARSELDINE ◽  
S. H. FERRIS ◽  
G. J. HUXHAM ◽  
S. W. MANLEY

Thyrotrophin (TSH), cyclic AMP, cyclic GMP and 1-methyl-3-isobutyl-xanthine (MIX) promoted the reassociation of isolated porcine and human thyroid cells into follicular structures in culture and stimulated the uptake of radio-iodide. Monolayer cells were present in all cultures, but in decreasing proportions as the concentration of stimulator was increased. The resting membrane potential of porcine thyroid cells cultured for 4 days in the presence of TSH was −54 ± 3·6 (mean ± s.d.) mV for follicular cells and −31 ± 2·6 mV for monolayer cells. In the absence of TSH, only monolayer cells were present and their membrane potential was −24 ± 2·0 mV. Removal of hormone by washing resulted in hyperpolarization to −70 ± 2·9 mV (follicular cells) or −59 ± 3·4 mV (monolayer cells). Subsequent replacement of TSH, or addition of cyclic AMP, MIX, prostaglandin E1 (PGE1) or long-acting thyroid stimulator immunoglobulin resulted in depolarization of previously hyperpolarized cells, to approximately the membrane potential observed before washing. Incubation in MIX resulted in enhanced sensitivity to the depolarizing effect of TSH. Cells cultured in the absence of TSH were unresponsive to TSH or other stimulators. The membrane potential of human thyroid cells behaved similarly in response to TSH, to hormone removal and replacement, and to MIX and PGE1.


FEBS Letters ◽  
1983 ◽  
Vol 157 (2) ◽  
pp. 323-329 ◽  
Author(s):  
Pierre P. Roger ◽  
Patricia Servais ◽  
Jacques E. Dumont

1990 ◽  
Vol 4 (3) ◽  
pp. 193-199 ◽  
Author(s):  
M. Chambard ◽  
D. Depetris ◽  
D. Gruffat ◽  
S. Gonzalvez ◽  
J. Mauchamp ◽  
...  

ABSTRACT Exocytosis, the ultimate step in thyroglobulin secretion, has been studied in porcine thyroid cells cultured in monolayers on the permeable bottom of culture chambers. We have previously demonstrated, using this culture system, that apical secretion accounts for 85–95% of total secretion of newly synthesized thyroglobulin. When cells were cultured for several days with bovine TSH (25 μU/ml) in the basal medium, the rate of glycoprotein accumulation in the upper compartment was three times higher than that in the absence of TSH. In contrast, the rate of thyroglobulin released into the basal medium (5–15% of total secreted thyroglobulin) appeared unmodified by chronic TSH stimulation. To investigate the effect of acute TSH stimulation on thyroglobulin exocytosis in the apical and basal compartments, pulse-chase experiments were carried out with the same culture system. The release of radiolabelled thyroglobulin (1·5-h pulse) into the apical medium was increased threefold during the 2-h chase period under TSH stimulation. The radiolabelled thyroglobulin released into the basal medium was increased only 1·5- to 2-fold, and stimulation disappeared after 1 h. The effect of TSH was maximal when the chase medium contained 50 μU TSH/ml. However, cells cultured for several days in the presence of 25 μU TSH/ml before the pulse-chase experiment, appeared desensitized to acute TSH stimulation. Similar responses were observed when the chase medium contained 8-chloro-cyclic AMP or cholera toxin. This study provides another example of the pleiotropic effect of TSH, mediated by cyclic AMP, on the sequential steps of thyroglobulin gene expression in cultured thyroid cells in which the polar character of the epithelial cells is well preserved.


1986 ◽  
Vol 15 (3) ◽  
pp. 289-301 ◽  
Author(s):  
V. Gallo ◽  
M. T. Ciotti ◽  
F. Aloisi ◽  
G. Levi

Nature ◽  
1979 ◽  
Vol 279 (5711) ◽  
pp. 336-338 ◽  
Author(s):  
G. F. ERICKSON ◽  
C. WANG ◽  
A. J. W. HSUEH

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