DIFFERENTIATION OF THE CORPUS-LUTEUM OF THE MINK (MUSTELA-VISON) - MITOGENIC AND STEROIDOGENIC POTENTIAL OF LUTEAL CELLS FROM EMBRYONIC DIAPAUSE AND POSTIMPLANTATION GESTATION
Da. Douglas et al., DIFFERENTIATION OF THE CORPUS-LUTEUM OF THE MINK (MUSTELA-VISON) - MITOGENIC AND STEROIDOGENIC POTENTIAL OF LUTEAL CELLS FROM EMBRYONIC DIAPAUSE AND POSTIMPLANTATION GESTATION, Biology of reproduction, 58(5), 1998, pp. 1163-1169
The mink corpus luteum (CL) involutes after ovulation and remains dorm
ant, synthesizing low amounts of progesterone until reactivated to ter
minate embryonic diapause. We examined the mitotic and steroid synthet
ic capacity of luteal cells from the diapause and postimplantation pha
ses of mink gestation. Cells from diapause divided in vitro, reaching
confluence in 7-8 days. Three phenotypes were distinguishable: a fusif
orm cell in whorls, a hypertrophied epithelioid cell, and a small epit
helioid cell. The first and second cell types divided in vitro after c
onfluence, evidenced by localization of proliferating cell nuclear ant
igen (PCNA) in their nuclei. The small epithelioid cells were present
in cell nests and showed no PCNA activity. Cells derived from reactiva
ted CL did not reach confluence and had no PCNA activity. Progesterone
accumulation was enhanced in luteal cells from diapause by LH, FSH, a
nd dibutyryl (Bu-2) cAMP, and by LH and (Bu-2)cAMP in cells from react
ivated CL. in luteal cells from the diapause phase of gestation, LH an
d (Bu-2)cAMP induced increases in mRNA coding for steroidogenic acute
regulatory protein, while cytochrome P450 side-chain cleavage enzyme m
RNA was increased by prolactin, LH and (Bu-2)cAMP. Cellular concentrat
ions of 3 beta-hydroxysteroid dehydrogenase-Delta(5-4)-isomerase mRNA
were increased by prolactin and (Bu-2)cAMP. Thus, luteinization in the
mink CL does not engender exit from the cell cycle, as both fusiform
and hypertrophied cells from diapause divide in vitro. Reactivation ap
pears to represent terminal differentiation. LH is capable of stimulat
ing steroidogenesis in vitro in luteal cells from diapause, and prolac
tin and LH appear to have both specific and overlapping stimulatory ef
fects on the CL of this species.