STEROIDOGENIC ACTIVITY, INSULIN-LIKE GROWTH-FACTOR-I PRODUCTION, AND PROLIFERATION OF GRANULOSA AND THECA CELLS OBTAINED FROM DOMINANT PREOVULATORY AND NONOVULATORY FOLLICLES DURING THE BOVINE ESTROUS-CYCLE - EFFECTS OF LOW-DENSITY AND HIGH-DENSITY-LIPOPROTEINS
B. Bao et al., STEROIDOGENIC ACTIVITY, INSULIN-LIKE GROWTH-FACTOR-I PRODUCTION, AND PROLIFERATION OF GRANULOSA AND THECA CELLS OBTAINED FROM DOMINANT PREOVULATORY AND NONOVULATORY FOLLICLES DURING THE BOVINE ESTROUS-CYCLE - EFFECTS OF LOW-DENSITY AND HIGH-DENSITY-LIPOPROTEINS, Biology of reproduction, 53(6), 1995, pp. 1271-1279
The role of high- and low-density lipoproteins (HDL and LDL) in regula
ting steroidogenic activity, cellular viability and proliferation, and
insulin-like growth factor-I (IGF-I) production was examined in granu
losa and theca cells from dominant preovulatory (DO) and nonovulatory
(DNO) bovine follicles. Follicles were obtained from pluriparous nonla
ctating beef cows at ovariectomy 24 h after administration of a luteol
ytic dose of prostaglandin F-2 alpha (DO) or during the first follicul
ar wave on Days 5-8 of the estrous cycle (DNO). Lipoprotein effects on
hormone production (ng/1.5 x 10(5) viable cells) and cell viability w
ere studied in serum-free, defined medium containing LH and FSH (granu
losa) or LH only (theca). During late stages (96-144 h) of culture, HD
L in the presence of gonadotropins increased (p < 0.001) the productio
n of progesterone by granulosa and theca cells and the production of I
GF-I by granulosa cells. LDL did not stimulate granulosa or thecal pro
gesterone synthesis and attenuated HDL-stimulated progesterone product
ion by both cell types. Gonadotropin stimulation of terminal synthetic
pathways was either attenuated (granulosa estradiol production) by ad
dition of lipoproteins or maximally stimulated (theca cell androstened
ione production) by a combination of LDL and HDL, Both lipoproteins in
creased (p < 0.05) granulosa cell viability in both follicle types, an
d a marked proliferation (p < 0.001) of steroidogenically inactive the
ca cells was observed from DO but not DNO follicles. Proliferation pot
ential appeared to be switched off during the late stages of maturatio
n of DNO follicles and switched on after induced luteal regression and
rescue of DO follicles.