Early Embryonic Development and Ovarian Activity During Concurrent Pregnancy and Lactation in the Hopping-Mouse Notomys Alexis.

1981 ◽  
Vol 29 (4) ◽  
pp. 589 ◽  
Author(s):  
WG Breed
Keyword(s):  
Epithelial Cell ◽  
Epithelial Cells ◽  
Embryonic Development ◽  
Steroid Hormone ◽  
Synthetic Activity ◽  
Luteal Cell ◽  
Ovarian Activity ◽  
Corpora Lutea ◽  
Pregnancy And Lactation ◽  
Further Development

In the hopping-mouse, following a postpartum mating, embryos enter the uterus on about day 5. Implantation occurs on about day 7 if there are no suckling pups, but zona-free blastocysts may remain up to day 18 if from four to seven suckling pups are present. Implantation is eccentric and initially involves interdigitation of trophectoderm and uterine epithelial cells, followed by epithelial cell displacement. The orientation is antimesometrial and, during further development, the embryo invaginates into the yolk-sac cavity. In the ovary, corpora lutea develop during the first few days of pregnancy and then remain unchanged in size or cellular morphology until implantation, regardless of the length of its delay. Peripheral progesterone levels likewise show little change during the preimplantation period. After implantation, a similar number of corpora lutea are found but they increase progressively in size due to luteal cell hypertrophy. The cells show all the organelles typical of steroid hormone synthetic activity and there is a corresponding increase in blood progesterone levels at this time. Vesicular follicles are present throughout concurrent pregnancy and lactation and are larger after implantation. There is no evidence of spontaneous ovulation except at the time of parturition.

ENDOCRINE PROFILES AND FUNCTIONAL CHARACTERISTICS OF CORPORA LUTEA FOLLOWING ONSET OF POSTPARTUM OVARIAN ACTIVITY IN BEEF COWS

1983 ◽  
Vol 63 (2) ◽  
pp. 331-347 ◽  
Author(s):  
J. G. MANNS ◽  
W. D. HUMPHREY ◽  
P. F. FLOOD ◽  
R. J. MAPLETOFT ◽  
N. RAWLINGS ◽  
...  
Keyword(s):  
Light And Electron Microscopy ◽  
Beef Cows ◽  
Luteal Cell ◽  
Cell Diameter ◽  
Rapid Decline ◽  
Ovarian Activity ◽  
Corpora Lutea ◽  
Functional Characteristics ◽  
Blood Samples ◽  
Endocrine Profiles

Three experiments were conducted to evaluate endocrine profiles and to determine the morphological and functional characteristics of corpora lutea (CL) following the onset of postpartum ovarian activity in beef cows, suckled by a single calf once daily. In exp. 1, blood samples were collected from 12 cows at 6-h intervals beginning 25 days postpartum until ovariectomy which was carried out on each of two cows on days 25, 27, 29, 31, 33, 35 after parturition. Ovarian structures were examined grossly and histologically. In exp. 2, blood samples were collected from eight cows at 6-h intervals for 18 days beginning 25 days postpartum and at less frequent intervals thereafter. Laparotomies were carried out on day 36 after calving, the ovaries were observed, CL were sampled and the residual tissue was marked with charcoal. A second laparotomy was performed on day 50. Luteal tissue samples were processed and examined by light and electron microscopy. Luteal cell types were evaluated, percent of area covered by large cells was determined and average luteal cell diameter was calculated. In exp. 3, seven cows were bled daily from parturition until day 25 postpartum. Serum from all experiments was assayed for progesterone (P4), FSH, LH and a prostaglandin metabolite (PGFM). The data showed that serum PGFM levels declined from a peak at calving to basal levels by 10 days postpartum which was well before the first ovulation. In all instances the observed peaks of serum LH and serum FSH preceded the first rise in P4 which, in eight of nine cases, was due to a functional CL. These CL were functional for periods of time ranging from 3 to 12 days. The regression of short-lived CL appeared abnormal compared to the longer-lived CL in which regression was characterized by a rapid decline in P4 and elevated blood PGFM. These data show clearly that the first increase in P4 is preceded by a typical LH surge, followed by ovulation and CL formation which has a variable life-span. Key words: Beef cows, postpartum, anestrus, corpus luteum.

Influence of rams on ovarian activity and oestrus in Merino ewes in the spring and early summer

1957 ◽  
Vol 8 (5) ◽  
pp. 460 ◽  
Author(s):  
HM Radford ◽  
RH Watson
Keyword(s):  
Epithelial Cells ◽  
Early Summer ◽  
Vaginal Epithelium ◽  
Ovarian Activity ◽  
Corpora Lutea ◽  
Group 4 ◽  
Group 6 ◽  
Almost All

The occurrence of oestrus and ovulation and the changes in the vaglnal contents were studied in Merino ewes following the introduction of vasectomized rams at various times during the spring and early summer. The ewes were in an anoestrous state when the observations were commenced. Except in occasional ewes oestrus did not appear until early December. It had occurred in all except a few ewes by early January. In most ewes among which rams were introduced on October 26 or November 18, it occurred about a week earlier than in ewes among which rams mere not introduced until December 8, and ewes among which rams had been running continuously. In at least 80 per cent, of animals in which both were studied, oestrus was accompanied by massive desquamation of the vaginal epithelium and it was preceded by one or more periods of massive desquamation. Between December 8 and December 14, masses of desquamated epithelial cells were present in the vaginal contents in few only of the ewes which were held separate from rams, but in almost all ewes among which rams were introduced on December 8 (group 4), and in most of the em7es which were running continuously with rams (group 6). They first appeared in the ewes of group 4 between December 11 and December 14, 3-6 days after the introduction of the rams, whereas they were already present in almost all of the ewes of group 6 by December 11.Corpora lutea compatible with ovulation shortly after December 8 were present in most ewes among which rams were introduced on that day, and in few ewes which were held separate from rams. The significance of these results is discussed.

scholarly journals Autocrine Growth Hormone Prevents Lactogenic Differentiation of Mouse Mammary Epithelial Cells

Endocrinology ◽  
2006 ◽  
Vol 147 (4) ◽  
pp. 1819-1829 ◽  
Author(s):  
Svetlana Mukhina ◽  
DongXu Liu ◽  
Ke Guo ◽  
Mireille Raccurt ◽  
Sahra Borges-Bendris ◽  
...  
Keyword(s):  
Epithelial Cell ◽  
Epithelial Cells ◽  
Mammary Epithelial Cell ◽  
Mammary Epithelial Cells ◽  
Three Dimensional ◽  
Late Pregnancy ◽  
Mammary Epithelial ◽  
Postnatal Ontogeny ◽  
Lactogenic Differentiation ◽  
Pregnancy And Lactation

We have examined the expression, postnatal ontogeny, and localization of mouse GH (mGH) and its relative expression during pregnancy, lactation, and weaning in the mouse. mGH mRNA and protein was expressed predominantly in the epithelial component of the mammary gland, and maximal expression was observed during the pubertal period. Autocrine mGH expression dramatically decreased during late pregnancy and lactation. Concordantly, autocrine mGH expression is repressed during forced differentiation of mouse HC11 mammary epithelial cells in culture. Forced expression of mGH in HC11 cells abrogated lactogenic differentiation as indicated by reduced expression of β-casein and reduced expression and loss of lateral epithelial localization of E-cadherin. Forced expression of mGH in mouse mammary epithelial cells increased cell survival and proliferation and consequently increased the size of mammary acinar-like structures formed in three-dimensional Matrigel. Thus, autocrine mGH expression in the mouse mammary epithelial cell is maximal at puberty and prevents mammary epithelial cell differentiation. Autocrine GH will therefore participate in mammary morphogenic processes at puberty.

Electron Microscopic Study of the Epithelium of the Seminal Vesicle of Aging Rats

1974 ◽  
Vol 32 ◽  
pp. 138-139
Author(s):  
V. F. Allison ◽  
G. C. Fink ◽  
G. W. Cearley
Keyword(s):  
Cell Growth ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Seminal Vesicle ◽  
Seminal Vesicles ◽  
Epithelial Layer ◽  
Epithelial Hyperplasia ◽  
Electron Microscopic ◽  
Aging Rats ◽  
Pseudostratified Epithelium

It is well known that epithelial hyperplasia (benign hypertrophy) is common in the aging prostate of dogs and man. In contrast, little evidence is available for abnormal epithelial cell growth in seminal vesicles of aging animals. Recently, enlarged seminal vesicles were reported in senescent mice, however, that enlargement resulted from increased storage of secretion in the lumen and occurred concomitant to epithelial hypoplasia in that species.The present study is concerned with electron microscopic observations of changes occurring in the pseudostratified epithelium of the seminal vescles of aging rats. Special attention is given to certain non-epithelial cells which have entered the epithelial layer.

Intranuclear Crystals in Regenerating Canine Kidneys

1973 ◽  
Vol 31 ◽  
pp. 412-413
Author(s):  
D.G. Osborne ◽  
L.J. McCormack ◽  
M.O. Magnusson ◽  
W.S. Kiser
Keyword(s):  
Epithelial Cell ◽  
Epithelial Cells ◽  
Tubular Epithelial Cell ◽  
Tubular Epithelial Cells ◽  
Cell Nuclei ◽  
Crystalline Structures ◽  
Small Crystals ◽  
Membrane Bound

During a project in which regenerative changes were studied in autotransplanted canine kidneys, intranuclear crystals were seen in a small number of tubular epithelial cells. These crystalline structures were seen in the control specimens and also in regenerating specimens; the main differences being in size and number of them. The control specimens showed a few tubular epithelial cell nuclei almost completely occupied by large crystals that were not membrane bound. Subsequent follow-up biopsies of the same kidneys contained similar intranuclear crystals but of a much smaller size. Some of these nuclei contained several small crystals. The small crystals occurred at one week following transplantation and were seen even four weeks following transplantation. As time passed, the small crystals appeared to fuse to form larger crystals.

Redistribution and dysfunction of integrins in cultured renal epithelial cells exposed to oxidative stress

1993 ◽  
Vol 264 (1) ◽  
pp. F149-F157 ◽  
Author(s):  
J. Gailit ◽  
D. Colflesh ◽  
I. Rabiner ◽  
J. Simone ◽  
M. S. Goligorsky
Keyword(s):  
Oxidative Stress ◽  
Cell Adhesion ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Cell Surface ◽  
Apical Cell ◽  
Flow Cytometric Analysis ◽  
Adhesion Properties ◽  
Renal Tubular Cells ◽  
Renal Tubular

Tubular obstruction by detached renal tubular epithelial cells is a major cause of oliguria in acute renal failure. Viable renal tubular cells can be recovered from urine of patients with acute tubular necrosis, suggesting a possible defect in cell adhesion to the basement membrane. To study this process of epithelial cell desquamation in vitro, we investigated the effect of nonlethal oxidative stress on the integrin adhesion receptors of the primate kidney epithelial cell line BS-C-1. Morphological and functional studies of cell adhesion properties included the following: interference reflection microscopy, intravital confocal microscopy and immunocytochemistry, flow cytometric analysis of integrin receptor abundance, and cell-matrix attachment assay. High levels of the integrin subunits alpha 3, alpha v, and beta 1 were detected on the cell surface by fluorescence-activated cell sorting (FACS) analysis, as well as lower levels of alpha 1, alpha 2, alpha 4, alpha 5, alpha 6, and beta 3. Exposure of BS-C-1 cells to nonlethal oxidative stress resulted in the disruption of focal contacts, disappearance of talin from the basal cell surface, and in the redistribution of integrin alpha 3-subunits from predominantly basal location to the apical cell surface. As measured in a quantitative cell attachment assay, oxidative stress decreased BS-C-1 cell adhesion to type IV collagen, laminin, fibronectin, and vitronectin. Defective adhesion was not associated with a loss of alpha 3-, alpha 4-, or alpha v-integrin subunits from the cell surface.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals c-Src inactivation reduces renal epithelial cell-matrix adhesion, proliferation, and cyst formation

2011 ◽  
Vol 301 (2) ◽  
pp. C522-C529 ◽  
Author(s):  
Justine Elliott ◽  
Nadezhda N. Zheleznova ◽  
Patricia D. Wilson
Keyword(s):  
Cell Proliferation ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Collecting Duct ◽  
Specific Inhibitor ◽  
Cell Phenotype ◽  
Epithelial Cell Proliferation ◽  
Matrix Adhesion ◽  
Cyst Lining

c-Src is a non-receptor tyrosine kinase whose activity is induced by phosphorylation at Y418 and translocation from the cytoplasm to the cell membrane. Increased activity of c-Src has been associated with cell proliferation, matrix adhesion, motility, and apoptosis in tumors. Immunohistochemistry suggested that activated (pY418)-Src activity is increased in cyst-lining autosomal dominant polycystic kidney disease (ADPKD) epithelial cells in human and mouse ADPKD. Western blot analysis showed that SKI-606 (Wyeth) is a specific inhibitor of pY418-Src without demonstrable effects on epidermal growth factor receptor or ErbB2 activity in renal epithelia. In vitro studies on mouse inner medullary collecting duct (mIMCD) cells and human ADPKD cyst-lining epithelial cells showed that SKI-606 inhibited epithelial cell proliferation over a 24-h time frame. In addition, SKI-606 treatment caused a striking statistically significant decrease in adhesion of mIMCD and human ADPKD to extracellular collagen matrix. Retained viability of unattached cells was consistent with a primary effect on epithelial cell anchorage dependence mediated by the loss of extracellular matrix (ECM)-attachment due to α2β1-integrin function. SKI-606-mediated attenuation of the human ADPKD hyperproliferative and hyper-ECM-adhesive epithelial cell phenotype in vitro was paralleled by retardation of the renal cystic phenotype of Pkd1 orthologous ADPKD heterozygous mice in vivo. This suggests that SKI-606 has dual effects on cystic epithelial cell proliferation and ECM adhesion and may have therapeutic potential for ADPKD patients.

scholarly journals Time- and Dose-Dependent Effects of 17 Beta-Estradiol on Short-Term, Real-Time Proliferation and Gene Expression in Porcine Granulosa Cells

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Sylwia Ciesiółka ◽  
Joanna Budna ◽  
Karol Jopek ◽  
Artur Bryja ◽  
Wiesława Kranc ◽  
...  
Keyword(s):  
Real Time ◽  
Granulosa Cells ◽  
Hormone Receptor ◽  
Proliferative Activity ◽  
Cell Transformation ◽  
Luteinizing Hormone Receptor ◽  
Luteal Cell ◽  
Ovarian Activity ◽  
Short Term

The key mechanisms responsible for achievement of full reproductive and developmental capability in mammals are the differentiation and transformation of granulosa cells (GCs) during folliculogenesis, oogenesis, and oocyte maturation. Although the role of 17 beta-estradiol (E2) in ovarian activity is widely known, its effect on proliferative capacity, gap junction connection (GJC) formation, and GCs-luteal cells transformation requires further research. Therefore, the goal of this study was to assess the real-time proliferative activity of porcine GCs in vitro in relation to connexin (Cx), luteinizing hormone receptor (LHR), follicle stimulating hormone receptor (FSHR), and aromatase (CYP19A1) expression during short-term (168 h) primary culture. The cultured GCs were exposed to acute (at 96 h of culture) and/or prolonged (between 0 and 168 h of culture) administration of 1.8 and 3.6 μM E2. The relative abundance of Cx36, Cx37, Cx40, Cx43, LHR, FSHR, and CYP19A1 mRNA was measured. We conclude that the proliferation capability of GCs in vitro is substantially associated with expression of Cxs, LHR, FSHR, and CYP19A1. Furthermore, the GC-luteal cell transformation in vitro may be significantly accompanied by the proliferative activity of GCs in pigs.

scholarly journals A Dual Role for Oncostatin M Signaling in the Differentiation and Death of Mammary Epithelial Cells in Vivo

2008 ◽  
Vol 22 (12) ◽  
pp. 2677-2688 ◽  
Author(s):  
Paul G. Tiffen ◽  
Nader Omidvar ◽  
Nuria Marquez-Almuina ◽  
Dawn Croston ◽  
Christine J. Watson ◽  
...  
Keyword(s):  
Gene Expression ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Mammary Epithelial Cells ◽  
Mammary Epithelial ◽  
Oncostatin M ◽  
Specific Gene ◽  
Mammary Involution

Abstract Recent studies in breast cancer cell lines have shown that oncostatin M (OSM) not only inhibits proliferation but also promotes cell detachment and enhances cell motility. In this study, we have looked at the role of OSM signaling in nontransformed mouse mammary epithelial cells in vitro using the KIM-2 mammary epithelial cell line and in vivo using OSM receptor (OSMR)-deficient mice. OSM and its receptor were up-regulated approximately 2 d after the onset of postlactational mammary regression, in response to leukemia inhibitory factor (LIF)-induced signal transducer and activator of transcription-3 (STAT3). This resulted in sustained STAT3 activity, increased epithelial apoptosis, and enhanced clearance of epithelial structures during the remodeling phase of mammary involution. Concurrently, OSM signaling precipitated the dephosphorylation of STAT5 and repressed expression of the milk protein genes β-casein and whey acidic protein (WAP). Similarly, during pregnancy, OSM signaling suppressed β-casein and WAP gene expression. In vitro, OSM but not LIF persistently down-regulated phosphorylated (p)-STAT5, even in the continued presence of prolactin. OSM also promoted the expression of metalloproteinases MMP3, MMP12, and MMP14, which, in vitro, were responsible for OSM-specific apoptosis. Thus, the sequential activation of IL-6-related cytokines during mammary involution culminates in an OSM-dependent repression of epithelial-specific gene expression and the potentiation of epithelial cell extinction mediated, at least in part, by the reciprocal regulation of p-STAT5 and p-STAT3.

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