scholarly journals Differential distribution of gelatinases and tissue inhibitor of metalloproteinase-1 in the rat ovary

1998 ◽  
Vol 158 (2) ◽  
pp. 221-228 ◽  
Author(s):  
P Bagavandoss

The distribution of gelatinases/matrix metalloproteinases-2 and -9 (MMP-2 and MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1) in neonatal and gonadotropin-primed immature rat ovaries was studied by immunofluorescent microscopy. Immature female Long-Evans rats were primed with 15 IU pregnant mare's serum gonadotropin (PMSG) in 100 microliters PBS. Two days later, to induce ovulation, the rats were injected with human chorionic gonadotropin (hCG, 5 IU/100 microliters PBS). The animals were killed at appropriate times and the ovaries removed and processed for cryostat or paraffin sectioning. Ovaries were also obtained from 7-day-old neonatal rats and processed as above. In the neonatal rat ovary, MMP-2 was present in the follicle and in the ovarian surface epithelium. MMP-9 was not detectable in the neonatal ovary. TIMP-1 was present in the oocyte and in the surface epithelium. In the PMSG-primed ovary, MMP-2 was present in the granulosa and thecal cells of the ovary. MMP-9 distribution, however, was restricted to the interstitial and thecal cells. TIMP-1 was mainly present in the blood vessels and thecal cells, with minor staining in the granulosa cells. In the developing corpus luteum, luteal and endothelial cells were positive for MMP-2. MMP-9 localization was restricted to the plasma membrane of the luteal and interstitial cells. TIMP-1 was clearly observed in the luteal capillaries and, to a lesser extent, in the luteal cell plasma membrane. This distribution of MMP-2, MMP-9, and TIMP-1 in the corpus luteum persisted throughout the life span of the corpus luteum. The spatial and temporal distribution of the gelatinases and TIMP-1 suggests unique roles for these proteins in the rat ovary.

1988 ◽  
Vol 116 (2) ◽  
pp. 307-312 ◽  
Author(s):  
T. A. Bramley ◽  
G. S. Menzies

ABSTRACT Homogenates of human corpus luteum were fractionated on continuous sucrose density gradients, with and without pretreatment with digitonin to perturb plasma membranes. Fractions of each gradient were assayed for steroid content and a range of plasma membrane and intracellular organelle markers. Progesterone and oestradiol were associated with a particulate fraction (buoyant density, 1·08–1·13 g/cm3). The buoyant density distribution of these steroids was distinct from those of the luteal cell plasma membrane and intracellular organelle markers tested. Treatment with digitonin increased the buoyant density of both progesterone and oestradiol. If steroids are contained in distinct vesicles, these vesicles may be involved in the sequestration of newly synthesized steroid and its movement to the cell surface for release into the circulation. J. Endocr. (1988) 116, 307–312


1969 ◽  
Vol 41 (3) ◽  
pp. 696-715 ◽  
Author(s):  
Eleanor C. Adams ◽  
Arthur T. Hertig

The ultrastructure of huma corpora luntea obtained approximately 2, 3, 5, 11, and 15 days after ovulation is reported. All specimens were fixed in Karnovsky's formaldehyde-glutaral-dehyde solution. The 5-day corpus luteum is presumed to represent, in terms of fine structure, the ultrastructural aspects of high progesterone production and is compared to younger differentiating and older regressing specimens. A distinct topographic relationship of cytoplasmic organelles is noted in the mature 5-day luteal cell. It consists of a peripheral cupshaped mass of tubular ER (endoplasmic reticulum), associated with granular ER, lipid droplets, and mitochondria, which merges with a large paranuclear Golgi area extending to a cell surface bordering a perivascular space. The plasma membrane of active luteal cells is described and its variations suggest areas of specialized surface activities. The prevalence and ultrastructure of more electron-opaque stellate cells, of phagocytes, and of thecal cells are reported.


Author(s):  
Amreek Singh ◽  
Warren G. Foster ◽  
Anna Dykeman ◽  
David C. Villeneuve

Hexachlorobenzene (HCB) is a known toxicant that is found in the environment as a by-product during manufacture of certain pesticides. This chlorinated chemical has been isolated from many tissues including ovary. When administered in high doses, HCB causes degeneration of primordial germ cells and ovary surface epithelium in sub-human primates. A purpose of this experiment was to determine a no-effect dose of the chemical on the rat ovary. The study is part of a comprehensive investigation on the effects of the compound on the biochemical, hematological, and morphological parameters in the monkey and rat.


Cancer ◽  
1998 ◽  
Vol 82 (7) ◽  
pp. 1359-1366 ◽  
Author(s):  
Hiro-omi Kanayama ◽  
Kin-ya Yokota ◽  
Yasushi Kurokawa ◽  
Yoshihide Murakami ◽  
Masaaki Nishitani ◽  
...  

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