scholarly journals Leucocyte proliferation in the bovine corpus luteum

Reproduction ◽  
2001 ◽  
pp. 297-305 ◽  
Author(s):  
M Bauer ◽  
I Reibiger ◽  
K Spanel-Borowski

Leucocytes vary in type and number during the lifespan of a corpus luteum. The aim of this study was to determine whether there is an increase in the number of lymphocytes and macrophages as a result of local proliferation. Bovine corpora lutea were classified into stages of development, secretion and regression. A new double immunolabelling method was established for nuclear Ki-67 antigen (a marker for cell proliferation) and for leucocyte surface antigens (detection of CD2-, CD3-, CD4-, CD8-positive lymphocytes and CD14-positive monocytes). Differential cell counting was performed. Between the stages of development and regression there was an increase in the number of T-lymphocytes and macrophages. The percentage of proliferating leucocytes in relation to the total number of proliferating cells was approximately 20% at the stage of advanced secretion and 70% at late regression. The increase in the number of proliferating leucocytes at late regression was due to CD14-positive macrophages. These macrophages migrated from small blood vessels into the septa of corpora lutea at the early stage of regression. Macrophages showed local proliferation in the late stage of regression when capillaries were no longer present. It is concluded that the physiological involution of the corpus luteum is an inflammatory-like condition, which includes local proliferation of monocytes.

1972 ◽  
Vol 69 (2) ◽  
pp. 369-384
Author(s):  
H. Brandau ◽  
L. Brandau ◽  
G. Mutzke

ABSTRACT In the bovine corpora lutea periodical activities of the Δ53β-, 3β-, 17β-and 20β-hydroxysteroid dehydrogenase (OHSDH) as well as activities of glyceraldehyde-3-phosphate- and glucose-6-phosphate dehydrogenase were measured quantitatively and the alterations throughout the different stages of the cycle were studied. After homogenization of the tissue and fractionate centrifugation the enzyme activities were determined by a standardized optical method. The activities of the Δ53β-, and 3β- and 17β-OHSDH increase slowly during the first 7 days of the cycle, the maximum is reached abruptly on the 12th to 13th day of the cycle. After a striking reduction the activities decline continually to the 19th to 21st day reaching the values detected at the beginning of the cycle. The 20β-OHSDH increases slowly to the maximum on the 15th day of the cycle. Activities of the 3α-OHSDH were obtained only inconsistently. The behaviour of the activities of G6PDH was nearly identical with that of the 3β-OHSDH, while the GAPDH shows only little fluctuations of its activities. The obtained enzyme activity patterns of the maturating and high functional corpus luteum correspond to the well-known data of the biosynthetic function of the bovine corpus luteum. The changes of the amounts of progesterone and 20β-progesterol agree with the course of the activities of the 3β- resp. 20β-OHSDH.


1996 ◽  
Vol 1996 ◽  
pp. 69-69
Author(s):  
AJ Holt ◽  
RG Rodway ◽  
JBC Findlay ◽  
HS Sands ◽  
DN Batchelder

The role of β-carotene in the fertility of ruminant animals has long been acknowledged (Friesecke, 1978). Initially this was thought to be due to its action as a vitamin A precursor but recently β-carotene itself has been considered responsible for improving reproductive performance (Hurley & Doane, 1989). The mechanism by which β-carotcne acts is unclear, but as its concentration in the corpus luteum was typically found to be 70μg per gram of tissue, its biological action is probably exerted in this area.β-Carotene has been studied in the bovine corpus luteum using Raman spectroscopy, high performance liquid chromatography (HPLC) and gel filtration chromatography. The structure of β-carotene produces a characteristic Raman spectrum and by utilising an imaging technique, photographs of isolated luteal cells were obtained indicating the regions of β-carotene within them. Differential centrifugation was used to obtain pure subcellular fractions of luteal cells.


2002 ◽  
Vol 75 (3) ◽  
pp. 427-432 ◽  
Author(s):  
Ş. Arikan ◽  
A. A. Yigit

AbstractThe present study examines the size distribution of ovine steroidogenic and non-steroidogenic luteal cells throughout pregnancy. Cells were isolated from corpora lutea collected from early (< 8 weeks), mid (9 to 14 weeks) or late (15 to 18 weeks) stages of pregnancy. Cells were stained for 3β-hydroxysteroid dehydrogenase (3β-HSD) activity, a marker for steroidogenic cells. Both 3β-HSD positive and β-HSD negative cells covered a wide spectrum of size ranging from 7 to 37 μm in diameter. There was a significant increase (P > 0·01) in mean diameter of non-steroidogenic luteal cells as pregnancy progressed. Mean diameter of 3β-HSD negative cells increased from 17·8 (s.e. 0·4) μm in the corpus luteum of early stage of pregnancy to 22·4 (s.e. 0·3) μm in the corpus luteum of advanced pregnancy. However, there was no significant increase in the mean diameter of 3β-HSD positive cells. Corpora lutea obtained from early stages of the pregnancy contained more steroidogenic cells than the cells obtained from mid and late pregnancy (P < 0·01). Percentage of 3β-HSD negative cells had increased 2·07-fold by 18 weeks of pregnancy when compared with the early stage of pregnancy. In contrast, percentage of 3β-HSD positive cells had decreased to 50% of starting values during the same period (P < 0·05). These results indicate that the ovine corpus luteum of pregnancy is morphologically dynamic over the course of pregnancy. Steroidogenic activity of luteal cells may decrease as pregnancy progresses, especially activity of the large luteal cells.


1996 ◽  
Vol 1996 ◽  
pp. 69-69
Author(s):  
AJ Holt ◽  
RG Rodway ◽  
JBC Findlay ◽  
HS Sands ◽  
DN Batchelder

The role of β-carotene in the fertility of ruminant animals has long been acknowledged (Friesecke, 1978). Initially this was thought to be due to its action as a vitamin A precursor but recently β-carotene itself has been considered responsible for improving reproductive performance (Hurley & Doane, 1989). The mechanism by which β-carotcne acts is unclear, but as its concentration in the corpus luteum was typically found to be 70μg per gram of tissue, its biological action is probably exerted in this area.β-Carotene has been studied in the bovine corpus luteum using Raman spectroscopy, high performance liquid chromatography (HPLC) and gel filtration chromatography. The structure of β-carotene produces a characteristic Raman spectrum and by utilising an imaging technique, photographs of isolated luteal cells were obtained indicating the regions of β-carotene within them. Differential centrifugation was used to obtain pure subcellular fractions of luteal cells.


1916 ◽  
Vol s2-61 (244) ◽  
pp. 433-473
Author(s):  
CHAS. H. O'DONOGHUE

The Corpus Luteum (a) Follicular Wall--The membrana granulosa in the three species, P. cinereus, T. vulpecula, and D. aurita, is composed of typical polygonal cells arranged three or four cells deep around the ripe follicle. The theca folliculi also calls for no special comment in any case. It is composed of internal and external layers, does not contain any included interstitial cells, and its cells are always readily distinguishable from membrana granulosa cells. (b) The Formation of the Corpus Luteum--The corpus luteum in P. cinereus is formed by the irruption of both layers of the theca folliculi, which burst through the membrana granulosa and form a lining on its inner side. This method of formation is similar to that in P. obesula, P. nasuta, and M. ruficollis. The ripe follicle in T. vulpecula collapses when the ovum is extruded, and the central cavity is at once obliterated. The theca folliculi is drawn in with the membrana granulosa, which it penetrates, and the connective tissue becomes irregularly distributed through the body. It is unlike the process in any other marsupial so far examined, but to a certain extent resembles that in the mouse. In D. aurita the thecal irruptions do not at once go through the membrana granulosa, but push it before them until the central cavity is practically filled in, and then they break through and form the central plug of connective tissue. In one example, a very early stage, mitoses were found in the cells of the membrana granulosa, as was also the case in P. obesula and P. nasuta. (c) The fully formed Corpus Luteum.--The corpus luteum in P. cinereus remains hollow even when fully grown, and the central cavity does not get filled in until some time after the birth of the young, apparently not until the gland has started to decline. This condition is apparently unique. In T. vulpecula the corpus luteum is fairly typical when full grown, save that its connective tissue is much more irregularly arranged than in other marsupials. The condition of the corpus in D. aurita is very similar to that in D. viverrinus In no case is the membrana granulosa shed, nor does the theca interna contribute to the lutein cells of the corpus luteum. The Interstitial Tissue. There is present in the ovary of certain species of marsupials a tissue which corresponds histologically to the interstitial tissue in the ovary of the higher mammals. The cells are always distinguishable from ordinary stroma cells, cells of the theca interna, old lutein cells, or the cells of an atresic follicle, and there is no evidence that any of the last three are at any time transformed into interstitial cells. Such cells are present in the pouch young of T. vulpecula before they could have been derived from any of the sources suggested above. Interstitial tissue is to be regarded as a tissue suigeneris, although it is possible that it may originate from modified stroma cells at a very early stage. The tissue is irregularly distributed in the various species of marsupials, and it is worthy of note that it is present in all the Diprotodontia and absent in the Polyprotodontia so far examined. It may be present only as a few small groups of cells or in such quantity as to form by far the largest part of the bulk of the ovary, excluding corpora lutea, as, for example, in P. penicillata. The tissue has a typical glandular appearance, but no satisfactory account of its function has yet been put forward, and in view of this and its irregularity it is preferable not to call it a gland, but retain the term interstitial tissue or cells.


2010 ◽  
Vol 83 (Suppl_1) ◽  
pp. 235-235
Author(s):  
Sineenard Jiemtaweeboon ◽  
Koumei Shirasuna ◽  
Sybille Raddatz ◽  
Hans-Joachin Schuberth ◽  
Akio Miyamoto

1991 ◽  
Vol 124 (2) ◽  
pp. 179-187 ◽  
Author(s):  
Winfried G. Rossmanith ◽  
Markus Schick ◽  
Reiner Benz ◽  
Christian Lauritzen

Abstract. While the regulation of progesterone secretion from the corpus luteum by LH has been convincingly demonstrated, the secretory patterns in the absence of any pituitary LH inputs are yet unclear. Consequently, we investigated the progesterone secretion by an in vitro perifusion system to characterize spontaneous progesterone release from the isolated bovine corpus luteum. Slices (120 mg) of midluteal corpora lutea were placed in perifusion chambers and continuously perifused by Medium-199 for 160-320 min. Progesterone was determined by radioimmunoassay in the effluent fractions collected at 2-min intervals. The spontaneous progesterone release from all bovine corpora lutea was pulsatile. Pulses were observed at mean (±sem) intervals of 17.7±1.5 min with amplitudes of 6.7±0.5 ng and release rates of 29.5±2.4 ng · ml−1 · (2 min)−1 (N=5). Addition of 6.7 nmol/l hCG to the perifusion medium appeared to increase the pulse amplitudes and release rates (195±25% over unstimulated conditions), but did not change the pulse frequencies (N=3). Perifusions with calcium-free medium containing 50 μmol/l verapamil and 20 mmol/l EGTA tended to suppress the pulse frequencies and amplitudes of this spontaneous progesterone release, whereas addition of hCG reversed this decrease again (N=3). When prostaglandin activity was inhibited by 100 μmol/l indomethacin added to the perifusion medium, both pulse frequencies and amplitudes of this progesterone release were enhanced (N=4). During perifusions with 100 μmol/l of the anti-progesterone ZK 96.734, both the pulse frequencies and amplitudes increased (N=4). These studies demonstrate an episodic progesterone release from the bovine corpus luteum perifused in vitro. The spontaneous progesterone secretion is independent of, but facilitated by gonadotropin secretion. This pulsatile progesterone secretion from the midluteal corpus luteum and its regulation by intraovarian factors may reflect an autonomous pulse generating mechanism.


1976 ◽  
Vol 83 (2) ◽  
pp. 393-401 ◽  
Author(s):  
M. Paloma de la Llosa-Hermier ◽  
Claude Hermier ◽  
Pedro de la Llosa

ABSTRACT The binding of luteinizing hormone (LH) to cow corpora lutea homogenates was studied using a tritium labelled hormone obtained by reductive methylation. The KD observed was 0.9 10−10 m and the number of sites was the equivalent of 0.4 10−15 moles per mg of wet tissue. The influence of the pH and temperature was examined. HCG and LH produced the same binding inhibition curves as did unlabelled methylated LH, suggesting that the binding properties of the derivative used for labelling LH were similar to those of native LH. The inhibitory activity of the subunits was extremely low (α-LH: 4%, β-LH: 1%). No significant inhibition was observed in the case of FSH or prolactin.


Reproduction ◽  
2003 ◽  
pp. 259-270 ◽  
Author(s):  
MO Al-zi'abi ◽  
ED Watson ◽  
HM Fraser

Precise pharmacological control of the corpus luteum is important in the manipulation of the oestrous cycle in mares. Angiogenesis plays a key role in the growth and regression of the corpus luteum; therefore, influencing the vasculature of the corpus luteum may offer a novel method for controlling its lifespan. In the present study, changes in angiogenesis and vascular expression of endothelial growth factor (VEGF) were evaluated throughout the luteal phase and after PGF(2alpha)-induced luteolysis. Corpora lutea were collected from mares in the early luteal phase (days 3-4), mid-luteal phase (day 10), early regression (day 14), late regression (day 17), and at 12 and 36 h after administration of PGF(2alpha) on day 10 of the oestrous cycle. Immunohistochemistry was used to localize Von Willebrand factor and Ki67 in endothelial and proliferating cells, respectively. VEGF mRNA and protein were localized by in situ hybridization and immunohistochemistry. The proliferation index of endothelial cells was intense in the early luteal phase. The early and mid-luteal phases were characterized by a dense network of capillaries. The microvasculature started to regress by day 14. After administration of PGF(2alpha), vasodilation was observed after 12 h, but after 36 h, luteal degeneration was accompanied by a significant decrease in vascularity. VEGF mRNA and protein were expressed mainly in the luteal cells during the early and mid-luteal phases and expression declined at early regression (day 14). However, immunostaining for VEGF protein was high in late luteal regression (day 17) and 36 h after PGF(2alpha) administration. These findings indicate a close temporal association between VEGF expression and angiogenesis in the equine corpus luteum during its functional lifespan.


Sign in / Sign up

Export Citation Format

Share Document