Rg. Richards et al., DIFFERENTIAL-EFFECTS OF LH AND PGE(2) ON PROGESTERONE SECRETION BY SMALL AND LARGE PORCINE LUTEAL CELLS, Journal of Reproduction and Fertility, 102(1), 1994, pp. 27-34
This study examined the effects of LH and PGE(2) on progesterone secre
tion by small and large porcine luteal cells with or without low-densi
ty lipoproteins. Corpora lutea were isolated from gilts 13-14 days aft
er administering gonadotrophins; enzymatically dissociated and small a
nd large cells were isolated by elutriation. Culture plates, 24-well,
were then seeded with 150 000 small or 30 000 large luteal cells suspe
nded in 1 ml M199 medium supplemented with 5 mu g insulin ml(-1), 40 n
g hydrocortisone ml(-1) and with or without low-density lipoproteins (
50 mu g cholesterol ml(-1)) or PGE(2). Cells were cultured for up to 2
4 h in a humidified incubator at 37 degrees C under 5% CO2 in air. The
low-density lipoproteins stimulated (P < 0.05) progesterone secretion
by large, but not small, luteal cells. Prostaglandin E(2) stimulated
(P < 0.05) progesterone production by large luteal cells in a dose-dep
endent manner, and the stimulatory effects of PGE(2) were greater (P <
0.05) in the presence than in the absence of low-density lipoproteins
. Progesterone secretion by small luteal cells was not significantly a
ffected by PGE(2). Progesterone production by small luteal cells was e
nhanced (P < 0.05) by LH, and the stimulatory effects of LH were great
er (P < 0.05) in the presence than in the absence of low-density lipop
roteins. In the absence of these lipoproteins, LH had no effect on pro
gesterone secretion by large luteal cells; however, in the presence of
low-density lipoproteins, LH increased (P < 0.05) progesterone secret
ion by large cells, though to a lesser (P < 0.05) extent than the effe
ct of LH on small cells. These data demonstrate that progesterone secr
etion by porcine luteal cells is stimulated differentially by LH and P
GE(2) and that small luteal cells are more responsive to LH and PGE(2)
acts primarily on large luteal cells.