Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
Add more filters










Database
Language
Publication year range
1.
Mol Cell Endocrinol ; 470: 219-227, 2018 07 15.
Article in English | MEDLINE | ID: mdl-29113831

ABSTRACT

The poor oocyte quality in older women has previously been linked to the depletion of the ovarian reserve of primordial follicles and an increase in granulosal apoptosis. Granulosa cells were collected from 198 follicles and individually analysed by flow cytometry. In the young IVF patients, the level of apoptosis was inversely proportional to the expression of bone morphogenetic protein (BMPR1B) and follicle stimulating hormone (FSH) receptors. Conversely, in the older patients this relationship became dysregulated. In the older patients, at the time of preovulatory maturation, the reduced apoptosis reflects the poor mitogenic growth turnover rate of healthy follicles rather than the death rate in an atretic follicle. Restoring an optimum receptor density and down-regulation of receptors may improve oocyte quality and the pregnancy rate in older women.


Subject(s)
Apoptosis , Bone Morphogenetic Protein Receptors, Type I/metabolism , Granulosa Cells/cytology , Granulosa Cells/metabolism , Ovarian Follicle/growth & development , Ovarian Reserve/physiology , Receptors, FSH/metabolism , Signal Transduction , Adult , Female , Fertilization in Vitro , Follicle Stimulating Hormone/pharmacology , Humans , Middle Aged , Ovarian Follicle/metabolism , Receptors, LH/metabolism , Young Adult
2.
Mol Cell Endocrinol ; 446: 40-51, 2017 05 05.
Article in English | MEDLINE | ID: mdl-28188844

ABSTRACT

The low take-home baby rate in older women in Australia (5.8%) undergoing IVF (5.8%) is linked to the depletion of the ovarian reserve of primordial follicles. Oocyte depletion causes an irreversible change to ovarian function. We found that the young patient FSH receptor and LH receptor expression profile on the granulosa cells collected from different size follicles were similar to the expression profile reported in natural cycles in women and sheep. This was reversed in the older patients with poor ovarian reserve. The strong correlation of BMPR1B and FSH receptor density in the young was not present in the older women; whereas, the LH receptor and BMPR1B correlation was weak in the young but was strongly correlated in the older women. The reduced fertilisation and pregnancy rate was associated with a lower LH receptor density and a lack of essential down-regulation of the FSH and LH receptor. The mechanism regulating FSH and LH receptor expression appears to function independently, in vivo, from the dose of FSH gonadotrophin, rather than in response to it. Restoring an optimum receptor density may improve oocyte quality and the pregnancy rate in older women.


Subject(s)
Infertility, Female/metabolism , Infertility, Female/pathology , Ovarian Follicle/metabolism , Ovarian Reserve , Receptors, FSH/metabolism , Receptors, LH/metabolism , Adult , Animals , Bone Morphogenetic Protein Receptors, Type I/metabolism , Estrogens/blood , Female , Fertilization in Vitro , Granulosa Cells/metabolism , Granulosa Cells/pathology , Humans , Infertility, Female/blood , Middle Aged , Ovarian Follicle/growth & development , Progesterone/blood , Reproducibility of Results , Sheep , Signal Transduction , Young Adult
3.
Mol Cell Endocrinol ; 425: 84-93, 2016 Apr 15.
Article in English | MEDLINE | ID: mdl-26805635

ABSTRACT

Reproductive ageing is linked to the depletion of ovarian primordial follicles, which causes an irreversible change to ovarian cellular function and the capacity to reproduce. The current study aimed to profile the expression of bone morphogenetic protein receptor, (BMPR1B) in 53 IVF patients exhibiting different degrees of primordial follicle depletion. The granulosa cell receptor density was measured in 403 follicles via flow cytometry. A decline in BMPR1B density occurred at the time of dominant follicle selection and during the terminal stage of folliculogenesis in the 23-30 y good ovarian reserve patients. The 40+ y poor ovarian reserve patients experienced a reversal of this pattern. The results demonstrate an association between age-induced depletion of the ovarian reserve and BMPR1B receptor density at the two critical time points of dominant follicle selection and pre-ovulatory follicle maturation. Dysregulation of BMP receptor signalling may inhibit the normal steroidogenic differentiation required for maturation in older patients.


Subject(s)
Aging/metabolism , Bone Morphogenetic Protein Receptors, Type I/metabolism , Infertility, Female/metabolism , Ovarian Follicle/metabolism , Ovarian Reserve , Adult , Female , Gene Expression Regulation , Humans , Infertility, Female/etiology , Signal Transduction , Young Adult
4.
Reproduction ; 150(2): 151-63, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25948249

ABSTRACT

The aim of the present study was to determine the direct cause of the mutation-induced, increased ovulation rate in Booroola Merino (BB) sheep. Granulosa cells were removed from antral follicles before ovulation and post-ovulation from BB (n=5) and WT (n=12) Merino ewes. Direct immunofluorescence measurement of mature cell surface receptors using flow cytometry demonstrated a significant up-regulation of FSH receptor (FSHR), transforming growth factor beta type 1, bone morphogenetic protein receptor (BMPR1B), and LH receptor (LHR) in BB sheep. The increased density of FSHR and LHR provide novel evidence of a mechanism for increasing the number of follicles that are recruited during dominant follicle selection. The compounding increase in receptors with increasing follicle size maintained the multiple follicles and reduced the apoptosis, which contributed to a high ovulation rate in BB sheep. In addition, we report a mutation-independent mechanism of down-regulation to reduce receptor density of the leading dominant follicle in sheep. The suppression of receptor density coincides with the cessation of mitogenic growth and steroidogenic differentiation as part of the luteinization of the follicle. The BB mutation-induced attenuation of BMPR1B signaling led to an increased density of the FSHR and LHR and a concurrent reduction in apoptosis to increase the ovulation rate. The role of BMPs in receptor modulation is implicated in the development of multiple ovulations.


Subject(s)
Apoptosis/genetics , Bone Morphogenetic Protein Receptors, Type I/genetics , Granulosa Cells/drug effects , Ovulation/genetics , Receptors, FSH/genetics , Receptors, LH/genetics , Animals , Apoptosis/drug effects , Apoptosis/physiology , Bone Morphogenetic Protein Receptors, Type I/antagonists & inhibitors , Bone Morphogenetic Protein Receptors, Type I/metabolism , Female , Flow Cytometry , Mutation/genetics , Mutation/physiology , Ovarian Follicle/anatomy & histology , Ovarian Follicle/physiology , Ovulation/drug effects , Ovulation/physiology , Pregnancy , Receptors, FSH/antagonists & inhibitors , Receptors, FSH/metabolism , Receptors, LH/antagonists & inhibitors , Receptors, LH/metabolism , Sheep, Domestic , Steroids/biosynthesis
5.
Australas Med J ; 5(12): 623-6, 2012.
Article in English | MEDLINE | ID: mdl-23382765

ABSTRACT

A group of individuals who share common beliefs form a culture in which they communicate their values and attributes about certain aspects of society. Sex education remains one of the early teachings that humans experience irrespective of the race or level of development of a given society. However, different cultures perceive sex education differently due to differences in attitudes and beliefs, leading to significant diversity in the management of sex education among different societies across the globe. Many studies have found that in a traditional society with a homogeneous culture, the foremost reason for the different approaches to sex education is related to traditional values, in addition to other factors such as religion and political belief. In order to improve sex education, and consequently, sexual health in a modern multicultural society such as Australia, it becomes imperative to identify the inconsistency in beliefs about sex education among individuals with different cultural backgrounds in the Australian population. In this report, the author highlights similarities and differences in the methods employed by certain cultures of the Australian population. The report considers the different cultural environments of specific societies, the prevalence of sex education in these societies and how culture influences the prevalence. The concluding thoughts reflect on the success of the education programs in Australia, based on the idea that resolving the problems of sex education needs support from a number of bodies within Australian society.

6.
Reprod Biomed Online ; 21(4): 474-84, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20833108

ABSTRACT

One concern during intracytoplasmic sperm injection (ICSI) is that selected spermatozoa may have increased levels of DNA damage; however, the available testing for this is largely destructive in nature and therefore unsuitable as a tool for sperm selection. One alternative selection process that has previously achieved pregnancies is the hypo-osmotic swelling test (HOST). This study reports that low HOST values of neat semen samples were significantly (P<0.001) associated with increased DNA damage identified by the DNA fragmentation index (DFI) from the sperm chromatin structure assay as well as the TdT-mediated dUTP nick-end labelling (TUNEL) assay. The HOST value was highly predictive of an abnormal DFI value by receiver operating characteristic curve analysis (P<0.001). Furthermore, when individual spermatozoa were assessed for both HOST status and DNA fragmentation by TUNEL, the key HOST-induced tail-swelling grades D, E and F were most commonly associated with high HOST values and were significantly (P<0.001) associated with minimal DNA damage regardless of the DNA status of the ejaculate. The application of HOST may be a valuable tool in the routine identification and selection of viable, DNA-intact individual spermatozoa for ICSI after further research to demonstrate its efficacy and safety.


Subject(s)
DNA Fragmentation , Spermatozoa/metabolism , Adult , Chromatin/metabolism , Chromatin/ultrastructure , Humans , In Situ Nick-End Labeling , Male , Middle Aged , Osmosis , Sperm Injections, Intracytoplasmic , Spermatozoa/ultrastructure
7.
Reproduction ; 138(4): 689-96, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19589856

ABSTRACT

The role of bone morphogenetic proteins (BMPs) in the regulation of ovarian function has been extensively investigated but the mechanism of regulation is not well understood. The aim of this study was to investigate the effect of mutation in the BMP receptor in Booroola sheep on the number of primordial follicles and rate of follicle recruitment in comparison with that in normal merino sheep in vivo. Whole sheep ovaries at the time of birth, 1.5 and 5 years old were collected and processed for the follicle quantification, using computerised stereological methods and statistical analyses. At birth, the total number of primordial follicles in Booroola sheep was significantly lower than in merino sheep. At 1.5 and 5 years, a reversed pattern in favour of Booroola ewes was seen with significantly more primordial follicles than merino. In parallel, the rate of primordial follicle recruitment to developing cohort was substantially lower in Booroola ewes with only 51 and 66% of primordial follicle consumption at 1.5 and 5 years respectively compared to 92 and 97% in merino ewes. On other hand, the mean numbers of developing primary follicles were smaller in Booroola sheep at the time of birth, yet, Booroola ewes possess more primary follicles than merino at 1.5 years. These findings suggest that attenuation of the intraovarian signalling pathway of BMPs may in fact be a successful means of rationalising follicle consumption, preventing unnecessary loss of follicles from the initial primordial follicle pool, hence increasing reproductive longevity and fertility.


Subject(s)
Bone Morphogenetic Proteins/metabolism , Ovarian Follicle/physiology , Sheep , Animals , Animals, Newborn , Bone Morphogenetic Protein Receptors/genetics , Bone Morphogenetic Protein Receptors/metabolism , Bone Morphogenetic Proteins/genetics , Bone Morphogenetic Proteins/physiology , Female , Models, Biological , Mutation/physiology , Ovarian Follicle/cytology , Ovulation/genetics , Ovulation/physiology , Progesterone/blood , Sheep/blood , Sheep/genetics , Sheep/metabolism , Sheep/physiology , Signal Transduction/genetics , Species Specificity
8.
J Pathol ; 206(1): 52-61, 2005 May.
Article in English | MEDLINE | ID: mdl-15772937

ABSTRACT

Early changes to branching morphogenesis of the prostate are believed to lead to enlargement of the gland in adult life. However, it has not been possible to demonstrate directly that alterations to branching during the developmental period have a permanent effect on adult prostate size. In order to examine branching morphogenesis in a quantitative manner in neonatal mice, a combination of imaging and computational technology was used to detect and quantify branching using bone morphogenetic protein 4 haplo-insufficient mice that develop enlarged prostate glands in adulthood. Accurate estimates were made of six parameters of branching, including prostate ductal length and volume and number of main ducts, branches, branch points, and tips. The results show that the prostate is significantly larger on day 3, well before the emergence of the phenotype in older animals. The ventral prostate is enlarged because the number of main epithelial ducts is increased; enlargement of the anterior prostate in mutant animals occurs because there are more branches. These lobe-specific mechanisms underlying prostate enlargement indicate the complex nature of gland pathology in mice, rather than a simple increase in weight or volume. This method provides a powerful means to investigate the aetiology of prostate disease in animal models prior to emergence of a phenotype in later life.


Subject(s)
Bone Morphogenetic Proteins/genetics , Image Processing, Computer-Assisted , Imaging, Three-Dimensional , Prostate/growth & development , Prostatic Hyperplasia/genetics , Animals , Animals, Newborn , Bone Morphogenetic Protein 4 , Bone Morphogenetic Proteins/deficiency , Homozygote , Male , Mice , Mice, Mutant Strains , Microscopy, Confocal , Morphogenesis/genetics , Prostate/metabolism , Prostate/pathology , Prostatic Hyperplasia/metabolism , Prostatic Hyperplasia/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...