Wc. Hymer et al., EXPERIMENTAL MODIFICATION OF RAT PITUITARY GROWTH-HORMONE CELL-FUNCTION DURING AND AFTER SPACEFLIGHT, Journal of applied physiology, 80(3), 1996, pp. 955-970
Space-flown rats show a number of flight-induced changes in the struct
ure and function of pituitary growth hormone (GH) cells after in vitro
postflight testing (W. C. Hymer, R. E. Grindeland, I. Krasnov, I. Vic
torov, K. Motter, P. Mukherjee, K. Shellenberger, and M. Vasques. J. A
ppl. Physiol. 73, Suppl.: 151S-157S, 1992). To evaluate the possible e
ffects of microgravity on growth hormone (GH) cells themselves, freshl
y dispersed rat anterior pituitary gland cells were seeded into vials
containing serum +/- 1 mu M hydrocortisone (HC) before flight. Five di
fferent cell preparations were used: the entire mixed-cell population
of various hormone-producing cell types, cells of density < 1.071 g/cm
(3) (band 1), cells of density > 1.071 g/cm(3) (band 2), and cells pre
pared from either the dorsal or ventral part of the gland. Relative to
ground control samples, bioactive GH released from dense cells during
flight was reduced in HC-free medium but tvas increased in HC-contain
ing medium. Band 1 and mixed cells usually showed opposite HC-dependen
t responses. Release of bioactive GH from ventral flight cells was low
er; postflight responses to GH-releasing hormone challenge were reduce
d, and the cytoplasmic area occupied by GH in the dense cells was grea
ter. Collectively, the data show that the chemistry and cellular makeu
p of the culture system modifies the response of GH cells to micrograv
ity. As such, these cells offer a system to identify gravisensing mech
anisms in secretory cells in future microgravity research.