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Biology of Reproduction, Vol 14, 613-626, Copyright © 1976 by Society for the Study of Reproduction
1 Reproduction Research Branch,
National Institute of child Health and Human Development,
National Institutes of Health,
Bethesda, Maryland 20014 The fine structure of granulosa lutein cells of the corpus luteum from pregnant monkeys
(Macaca mulatta) is described. Corpora lutea were obtained within the span of expected normal
delivery from intact mothers, as well as from mothers which were hypophysectomized (56-73
days), and those which were fetectomized (107-119 days) with the placentas maintained in situ
until near expected time of delivery. The gramulosa luteim cells from all groups had fine structural
characteristics indicative of active steroidogenesis. The slight differences in the fine structure of
these granulosa cells involved factors of concentration and size, as well as appearance of several
organelles. Cells of the corpus luteum from hypophysectomized animals had smaller mitochondria,
often associated with lamellar structures, and microfilaments occurred more frequently than in
intact animals. Mitochondria in the luteal cells from fetectomized monkeys with large osmiophilic
inclusions were more numerous and agranular ER and Golgi were increased when compared to
luteal cells from intact or hypophysectomized animals. Initial luteolysis was noticed in the CL of
intact and hypophysectomized monkeys, but to a lesser extent in the fetectomized animals. Onset
of luteolysis was indicated by obliteration of some blood vessels, shrinkage of cells and their nuclei,
and distention of the cisternae of the granular endoplasmic reticulum. Dense fibrillar structures and
collagen fibers accumulated in some of the perivascular and extracellular spaces. Various nexuses
were formed at areas of contact of cellular projections and the cell surface in every group of
monkeys. Fine structural features of CL from late pregnancy in rhesus monkeys support other
evidence that these granulosa lutein cells are active in steroid synthesis.
Accepted on February 10, 1976
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