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Biomedical subjects

L Selwood

Publications and source records attributed to L Selwood.

At least 19 recordsLinked to original sources

Identification of a homologue of POU5F1 (OCT3/4) in a marsupial, the brushtail possum.

Several morphological features of early development differ between marsupials and eutherians. These include early overt conceptus polarity, the mode of segregation of pluriblast and trophoblast lineages, and the superficial position of the pluriblast within the unilaminar blastocyst epithelium. Knowledge of the molecular mechanisms of early development is lacking in marsupials. We have cloned from the brushtail possum, Trichosurus vulpecula, the partial cDNA of a marsupial homologue of mammalian POU5F1, which encodes octamer-binding transcription factor-4 (Oct-4). The 579 bp cloned coding sequence of possum POU5F1 (tvPOU5F1) shares 74, 78, and 79% identity with murine Pou5f1, human POU5F1, and bovine bPOU5F1, respectively, at the protein level. The mRNA for tvPOU5F1 was detected by in situ hybridization in oogonia and in oocytes of growing follicles, but not in early meiotic oocytes. In a gastrulation-stage conceptus, high tvPOU5F1 expression was found in the embryonic ectoderm, with low or undetectable expression in other cell types. These results are comparable with those of murine and bovine expression studies, and suggest that the putative role of POU5F1 in totipotent and pluripotent cells is conserved among mammals.

Amino Acid Motifs↗

Ultrastructure of oogenesis in the brushtail possum.

Marsupial ova are slightly larger on average than those of eutherians. They have often been described as "yolky", although the nature and roles of their contents in later development are poorly understood. In the ova of all marsupial species studied, large quantities of electron-lucent vesicles are present. This study describes the ultrastructure of oogenesis in the brushtail possum, Trichosurus vulpecula. Oocytes of primordial follicles contain a variety of organelles of unknown function, some of which have been described previously in bandicoots. Large electron-lucent vesicles begin to accumulate after the transition from primordial follicle to primary follicle and are derived at least partly from the Golgi and endoplasmic reticulum. Other inclusions that are absent in some other marsupial species are present in growing possum oocytes in smaller quantities, including yolklike lipid bodies and electron-dense granular bodies.

Animals↗

Oogenesis in the marsupial stripe-faced dunnart, Sminthopsis macroura.

The timetable of oogenesis in Sminthopsis macroura is accelerated like in other marsupials showing relatively early maturation of the female. On the day of parturition (day 0) migration of primordial germ cells to the indifferent gonads has been completed. Follicular growth seems not to correspond to the biphasic pattern, in which oocyte and follicle grow synchronously until antral stages when only the follicle increases in size, but shows a continuous growth of the oocyte and the follicle up to the time of ovulation. During primordial and early primary follicle stage a paranuclear complex is present in the oocyte, consisting mainly of smooth tubules of endoplasmic reticulum. Cortical granules appear early in oocytes in secondary follicles. The conspicuous inclusions in the antral follicle are the clusters of electron-lucent vesicles in the oocyte. These inclusions grow from multivesicular bodies (MVB), which are formed from Golgi and endoplasmic reticulum vesicles. Further increase in the size of MVB involves the incorporation of endocytic vesicles and the coalescence of larger vesicles. The polarized nature of the oocyte at ovulation is due in part to the to accumulation of these vesicles in the cytoplasm opposite the eccentrically placed nuclear material.

Animals↗

Mechanisms for pattern formation leading to axis formation and lineage allocation in mammals: a marsupial perspective.

Developing patterns in early embryogenesis are analysed in conceptuses from several families, including Dasyuridae, Phalangeridae, Macropodidae and Didelphidae, in which cleavage has been examined in some detail. Features common to cleavage and blastocyst formation, and in some cases to hypoblast formation, are used to develop an outline of possible mechanisms leading to axis formation and lineage allocation. Relevant features that have been described only in some species are also included. It is suggested that certain features of marsupial cleavage establish patterns in the developing blastocyst epithelia, pluriblast, trophoblast and hypoblast that contribute to axis formation and lineage allocation. All marsupials examined had a polarized oocyte or conceptus, the polarity of which was related to the conceptus embryonic-abembryonic axis and, eventually, the conceptus dorsal-ventral axis and the formation of the pluriblast (future embryo) and trophoblast. The embryonic dorsal-ventral and anterior-posterior axes were established after the allocation of hypoblast and epiblast. Mechanisms that appear to result in patterning of the developing epithelia leading to axis formation and lineage allocation are discussed, and include sperm entry point, gravity, conceptus polarity, differentials in cell-zona, cell-cell and cell-type (boundary effects) contacts, cell division order during cleavage and signals external to the conceptus. A model of the patterning effects is included. The applicability of these mechanisms to other amniotes, including eutherian mammals, is also examined.

Animals↗

Significance of serum early pregnancy factor concentrations during pregnancy and embryonic development in Sminthopsis macroura (Spencer) (Marsupialia: Dasyuridae).

Marsupial pregnancy differs from that in eutherians in duration, placentation and hormonal profile so much so that maternal recognition of pregnancy may not occur in polyovular marsupials. However, a comparison of gravid and non-gravid uteri reveals differences indicative of histological and physiological adaptations to pregnancy. In the present study, the hypothesis that embryo-maternal signalling occurs in polyovular marsupials was tested by examining serum from non-pregnant and pregnant Sminthopsis macroura for the presence of early pregnancy factor (EPF), a serum protein secreted by the ovary in response to the presence of a newly fertilized egg in the oviduct. EPF is detectable in the serum of pregnant, but not in non-pregnant, females in all eutherians studied to date. In the present study, EPF was detected in S. macroura serum by the rosette inhibition test during the first 9 days of the 10.7 day gestation period in this marsupial. However, EPF was not detected on day 10, just before parturition, or in non-pregnant or preovulatory animals. Immunohistochemical analysis of ovaries from gravid and non-gravid animals demonstrates that EPF is found in the capillaries, interstitial spaces and secretory cells of the corpus luteum. It is concluded that the spatiotemporal pattern of EPF activity described strongly indicates that maternal recognition of pregnancy in marsupials is mediated, at least in part, by EPF. Because the endocrinological milieu is the same in pregnant and non-pregnant marsupials, the possibility of using marsupials as an experimental system for studying EPF function unconfounded by hormonal effects is presented.

Animals↗

Induced ovulation, mating success and embryonic development in the stripe-faced dunnart, Sminthopsis macroura.

Induced ovulation resulting in normal embryos is rare in marsupials. In this study natural and induced ovulations were compared in mature Sminthopsis macroura (n = 122). Comparison of maturation of preovulatory oocytes by ovarian histology and examination of oocytes removed from developing follicles in 12 ovaries of 23 animals receiving 0.058 iu equine serum gonadotrophin (eSG) g(-1) with ovaries of 12 animals undergoing natural cycles showed that oocyte maturation was significantly more irregular when it was induced (P < 0.001). Postovulatory stages were examined by estimating the number of eggs ovulated from ovarian histology, and by counting oviduct and uterine contents recovered after ovulation. S. macroura receiving 0.087 iu eSG g(-1) (n = 34), administered as one (n = 17) or two (n = 17) injections, were significantly (P < 0.05) more likely to ovulate (74%), mate (80%) and have conceptuses (66%) than were animals receiving 0.058 iu eSG g(-1) (12, 53 and 0%, respectively) (n = 17), and the values were similar to those in animals (n = 36) undergoing natural cycles (100, 81 and 56%, respectively). Induced ovulation using 0.087 iu eSG g(-1) yielded significantly (P < 0.05) more oocytes per ovary (20.8 +/- 8.5; combined data) than did ovulation in animals undergoing natural cycles (13.7 +/- 3.2) (ANOVA, t test). The responses of animals induced in different phases of the oestrous cycle with 0.087 iu eSG g(-1) were not significantly different (ANOVA) with respect to the number of corpora lutea per ovary, conceptuses per animal or days to ovulation after injection. However, the proportion of females that responded after receiving 0.058 iu eSG g(-1) in the luteal phase was significantly different from that in animals treated with the same dose in the intermediate phase (P < 0.01) and in non-cyclic females treated with 0.058 iu eSG g(-1) (P < 0.02). The main benefits of the treatment were that normal embryos resulted and that 70-78% of non-cyclic animals could be induced to ovulate.

Anestrus↗

cDNA cloning, characterization, expression and recombinant protein production of leukemia inhibitory factor (LIF) from the marsupial, the brushtail possum (Trichosurus vulpecula).

A reverse transcription technique using RNA templates combined with polymerase chain reaction (RT-PCR) was used to clone the cDNA fragment encoding the amino acid sequence of mature LIF protein of the marsupial, the brushtail possum, Trichosurus vulpecula. A PCR product with expected size, of 546bp, and termed tvLIF, was obtained using cDNA reverse-transcribed from total RNA isolated from possum uterus. A genomic DNA fragment (about 650bp) between the specified primers was also amplified, indicating the similarity in structure and organization of this gene and LIF genes from studied eutherian species, although the full-length of its cDNA and genomic DNA needs to be further clarified. The deduced amino acid sequence of tvLIF shows a high level of sequence identity and similar molecular characteristics to eutherian LIF, which suggests similar biological actions of this molecule in this marsupial. Because the expression of LIF gene in other mammalian species has been found to be at very low levels and its transcripts cannot be detected by Northern hybridization analysis, the expression pattern of tvLIF in adult tissues and reproductive tracts during early development was investigated using the RT-PCR technique. Resultant products of the RT-PCR were further analyzed by Southern hybridization using tvLIF as a probe. tvLIF transcripts were detected in most of the adult tissues and in the reproductive tracts of pregnant females. These results lend support to the idea that LIF contributes to the maintenance of pregnancy in this marsupial.

Amino Acid Sequence↗

Marsupial egg and embryo coats.

Egg and embryo coats of marsupials are reviewed. Marsupial eggs are enclosed by a zona pellucida, mucoid coat and an outer shell coat. An extra-cellular matrix coat that lines the zona pellucida also occurs in some species. The zona pellucida consists of three zona proteins (ZPA, ZPB, ZPC) with considerable similarity to those of eutherian mammals. The zona is thought to be the sperm receptor site and, in some species, but not others, is a barrier to polyspermy. Immunostaining, in situ hybridisation, histochemistry and electron microscopy indicate that the zona originates in the oocyte at the onset of oocyte growth. It changes greatly in shape during ovulation and early development and plays an essential role in blastocyst formation. The mucoid coat is an acid glycoprotein that is produced by non-ciliated cells at all levels of the oviduct and has been implicated in providing a barrier to polyspermy, nourishment of the embryo and an osmotically stable environment for the embryo. Its width varies widely in marsupials. The shell coat is secreted by the epithelia of the utero-tubal junction and upper uterus during oestrus and early cleavage. Evidence is provided for a second wave of secretion at bilaminar and trilaminar blastocyst stages. Shell-free embryos do not survive in vitro during bilaminar and early trilaminar blastocyst stages. Hatching from the shell coat occurs between 65 and 85% of the gestation period usually when the embryo is undergoing early somitogenesis. The extra-cellular matrix is secreted by the oocyte or by the cells of early cleavage stages and initially separates cells from the zona pellucida and from each other. It plays an essential role in blastocyst formation. The zona, mucoid and shell coats provide a framework for blastocyst construction and normal embryos do not form in their absence in some species.

Animals↗

A staging scheme for assessing development in vitro of organogenesis stage embryos of the stripe-faced dunnart, Sminthopsis macroura (Marsupialia: dasyuridae).

The inaccessibility of mammalian organogenesis stage embryos has precluded their widespread use in embryological and teratological studies. As organogenesis occurs during the last 1.5 days of the 10. 7 days of gestation in the stripe-faced dunnart (Sminthopsis macroura), the aim of the present study was to investigate whether day 9 and day 10 embryos and fetuses could be grown to term in vitro. High glucose Dulbecco's modified Eagle's medium with 10% fetal calf serum (FCS) supported embryonic growth for various periods of time, some to within 5 h of the predicted time of parturition. A roller culture system maintained at 35 degrees C was used to incubate organogenesis stage embryos (n = 43). Nine unincubated (control) embryos were either fixed for microscopic analysis or frozen for microprotein determination. The results of the present study indicate that with some optimization of the culture conditions (increasing oxygen in the gas phase in the culture tubes, replacing FCS with rat serum), it might be possible for organogenesis stage S. macroura embryos to be grown to term. A scoring scheme for assessing morphological development was devised for use as a standard in staging organogenesis stage embryos. This scheme reflects the highly compressed schedule of developmental events that occurs mainly during day 9 of gestation in S. macroura embryos. In comparison, during embryogenesis in Didelphis virginiana these developmental events occur from day 8 to day 10.5 of gestation, and birth occurs on day 13.

Animals↗

An ultrastructural study of the role of an extracellular matrix during normal cleavage in a marsupial, the brushtail possum.

In marsupials, the mechanisms of lineage allocation into pluriblast and trophoblast are related to conceptus polarity and polarized discharge of extracellular matrix (ECM). The brushtail possum, Trichosurus vulpecula, a major pest species in New Zealand, is being intensively studied to develop an immunocontraceptive control method. Of 23 specimens examined, 11 were examined by electron microscopy to study the presence and role of the ECM in lineage allocation in the possum. A number of polarized features in the zygote identified the future embryonic and abembryonic poles. Pronuclei, in a broad band of mitochondrion-rich cortical cytoplasm, lay in the embryonic hemisphere, and numerous electron-lucent vesicles characterized the abembryonic cytoplasm. These vesicles seemed to contribute to the ECM. During cleavage, cells lay near the zona in the embryonic hemisphere, and ECM accumulated chiefly in the abembryonic hemisphere. Cell-zona adhesion facilitated by microvillous and club processes occurred at the early 4-cell stage, and cell-cell adhesion commenced at the late 4-cell stage. The first two cleavages were meridional, equal, and accompanied by elimination into the cleavage cavity of much of the electron-lucent vesicular material in the form of several membrane-bound yolk masses. The third cleavage was unequal, with both meridional and latitudinal planes. The first differences between trophoblast and pluriblast lineages appeared at the 8-cell stage. Later cleavage planes were latitudinal or oblique. Conceptus polarity, polarized discharge of ECM, and localized cell-zona adhesion were related to the first lineage allocation in the possum.

Animals↗

Antiserum to the egg coats of the fat-tailed dunnart (Marsupialia, Dasyuridae) cross-reacts with egg coats of other marsupial and eutherian species.

We are examining the extracellular coats of the brush-tailed possum as a possible target for an immunocontraceptive vaccine for biocontrol of this pest species in New Zealand. In this study we have compared the composition of the extracellular coats of the fat-tailed and stripe-faced dunnarts, brush-tailed possum, domestic rabbit, and laboratory mouse using histochemistry, immunocytochemistry, and immunofluorescence. The histochemistry of the luminal epithelium of the oviduct and mucoid coats of the marsupials and rabbit indicated that they contain acidic glycoproteins. Immunofluorescence showed that polyclonal antiserum raised against the extracellular coats of the oocyte and early embryo of the fat-tailed dunnart, cross-reacted with the extracellular coats of the oocytes of all five species. These results suggest that there are common epitopes on the extracellular coats of oocytes and early embryos of distinctly related therian species. Further work to characterise these proteins is required to determine whether there is close homology between the oviductal glycoproteins of these species.

Animals↗

There is no highly conserved embryonic stage in the vertebrates: implications for current theories of evolution and development.

Embryos of different species of vertebrate share a common organisation and often look similar. Adult differences among species become more apparent through divergence at later stages. Some authors have suggested that members of most or all vertebrate clades pass through a virtually identical, conserved stage. This idea was promoted by Haeckel, and has recently been revived in the context of claims regarding the universality of developmental mechanisms. Thus embryonic resemblance at the tailbud stage has been linked with a conserved pattern of developmental gene expression - the zootype. Haeckel's drawings of the external morphology of various vertebrates remain the most comprehensive comparative data purporting to show a conserved stage. However, their accuracy has been questioned and only a narrow range of species was illustrated. In view of the current widespread interest in evolutionary developmental biology, and especially in the conservation of developmental mechanisms, re-examination of the extent of variation in vertebrate embryos is long overdue. We present here the first review of the external morphology of tailbud embryos, illustrated with original specimens from a wide range of vertebrate groups. We find that embryos at the tailbud stage - thought to correspond to a conserved stage - show variations in form due to allometry, heterochrony, and differences in body plan and somite number. These variations foreshadow important differences in adult body form. Contrary to recent claims that all vertebrate embryos pass through a stage when they are the same size, we find a greater than 10-fold variation in greatest length at the tailbud stage. Our survey seriously undermines the credibility of Haeckel's drawings, which depict not a conserved stage for vertebrates, but a stylised amniote embryo. In fact, the taxonomic level of greatest resemblance among vertebrate embryos is below the subphylum. The wide variation in morphology among vertebrate embryos is difficult to reconcile with the idea of a phyogenetically-conserved tailbud stage, and suggests that at least some developmental mechanisms are not highly constrained by the zootype. Our study also highlights the dangers of drawing general conclusions about vertebrate development from studies of gene expression in a small number of laboratory species.

Amphibians↗

Early cleavage to formation of the unilaminar blastocyst in the marsupial Antechinus stuartii: ultrastructure.

The development of Antechinus stuartii from the 2-cell stage to the blastocyst stage in vivo was examined by routine transmission electron microscopy. The 2-8-cell stages had a similar organization of organelles, whereas the 16- to 32-cell stages had pluriblast cells and trophoblast cells forming an epithelium closely apposed to the zona pellucida. Specialized cell-zona plugs were formed at the 8-cell stage, and primitive cell junctions appeared in later conceptuses. The cytoplasmic organelles included mitochondria, lysosomes, aggregates of smooth endoplasmic reticulum, lipid and protein yolk bodies and fibrillar arrays, possibly contractile in function. Nuclei had uniformly-dispersed dense chromatin. Nucleoli of 2-4-cell conceptuses were dense, compact and fibrillar, and those of 8-cell conceptuses and later conceptuses were finely granular and became progressively reticulated. The embryonic genome is probably not switched on before the 8-cell stage. Sperm tails were detected in cells in several early conceptuses. The yolk mass had the same organelles as cells. Centrioles were discovered for the first time in marsupial conceptuses. These were prominently situated at a spindle pole in a 32-cell blastomere and were associated with a nucleus and sperm tail at the 4-cell stage. It is very likely that the paternal centrosome is inherited at fertilization and perpetuated in Antechinus embryos during cleavage.

Animals↗

Histological differences between gravid and non-gravid uteri in the dasyurid marsupial, Sminthopsis macroura (Spencer).

Uterine samples from pregnant Sminthopsis macroura representing the first 10 days of its 11 day gestation period and samples from non-pregnant animals were compared histologically and examined for differences in the following characteristics: thickness of the endometrial stroma, luminal epithelium, myometrium and glandular epithelium, and the density of stromal glands and number of lymphocytes at the endometrial basal lamina. A highly significant difference between gravid and non-gravid uteri with respect to thickness of the endometrial epithelium was found on day 3, when lineage divergence occurs between the pluriblast and trophoblast. The endometrial stroma was significantly thicker in pregnant animals on day 8, when the epiblast differentiates into ectoderm, endoderm and mesoderm. Other differences between gravid and non-gravid uteri were detected in myometrial thickness on days 1 and 5. Taken together, these results indicate that despite similar endocrinological profiles of pregnant and non-pregnant marsupials, there are subtle, but significant, differences in uterine histology. The observed concordance between histological differences and differentiative events in embryogenesis is considered is indicative of embryo-maternal signalling.

Analysis of Variance↗

Development in vitro of Marsupials: a comparative review of species and a timetable of cleavage and early blastocyst stages of development in Monodelphis domestica.

The development of marsupial oocytes and embryos in vitro is reviewed. Most stages of development have been cultured successfully, usually in a complex medium with added fetal calf serum. Simpler media without added serum have been developed for fertilization and cleavage in vitro. Culture systems have been established for oocyte maturation and fertilization in the grey short-tailed opossum and for cleavage from the zygote to the early expanding unilaminar blastocyst in a number of other marsupials. Survival in vitro of the unilaminar and early bilaminar blastocyst stages is limited in all species examined. In contrast, late bilaminar, trilaminar, embryonic and fetal stages develop at rates approximating those in vivo. More stages have been cultured successfully in Sminthopsis macroura than in any other species. It has been cultured from the late bilaminar blastocyst to within 18 h of birth. Stages of cleavage and unilaminar blastocyst formation of Monodelphis domestica timed by videotaping mating animals, proceeded at similar rates in vivo and in vitro. As in other marsupials, cleavage in this opossum is characterized by a polarized conceptus. This polarity is expressed in the distribution of organelles in the zygote and the localization of secretion of the extracellular matrix material into the cleavage cavity and of the initial cell-zona attachment. Because cell-cell adhesion follows cell-zona adhesion, a unilaminar blastocyst forms without the development of an intervening morula stage.

Animals↗

A light microscopic study of oogenesis in the brushtail possum Trichosurus vulpecula.

Ovaries from young of the brushtail possum, Trichosurus vulpecula, were examined histologically and histochemically to determine stages of oogenesis. Groups of dividing oogonia were first present in a 13-day-old pouch young, with extensive oogonial proliferation after about 23 days of age. Meiosis was initiated in some oogonia by 48 days of age, and by 88 days numerous early primordial follicles were present. The first primary follicles had formed by 103 days of age. In oocytes of quiescent primordial follicles, dark granular material, which stained positively for protein, mainly occupied the perinuclear cytoplasm. Associated with the transition to primary follicles and continuing throughout oocyte growth was the production within the central cytoplasm of large clear vesicles and, to a lesser extent, lipid-like yolk bodies. The former were analogous to similar vesicles found in other species of marsupial, and have a putative role in development of the blastocyst. By contrast, yolk-like bodies are not found in all marsupial oocytes and their importance in development is unknown.

Animals↗

Nutrient uptake and culture of Sminthopsis macroura (stripe-faced dunnart) embryos.

Glucose and pyruvate uptake by individual embryos were measured in a marsupial species (stripe-faced dunnart) and a eutherian species (mouse). At each stage of development, nutrient uptake by the dunnart embryo was around an order of magnitude greater than that of the mouse embryo. The pattern of glucose uptake by the dunnart embryo was not like that for any eutherian embryo, all of which have a low glucose uptake before the blastocyst stage. Rather, in the dunnart embryo there was a significant increase in glucose uptake after the third cleavage division, increasing from 13.6 pmol embryo h-1 at the 4-cell stage to 34.9 pmol embryo h-1 by the 8-cell stage. This increase in glucose uptake before blastocyst formation may be attributed to an increased energy demand associated with the movement of cells within the dunnart embryo. Using a new culture system, it was possible to culture 66% of dunnart embryos at the 2-4-cell stage and 80% of those at the 8-16-cell stage to the unilaminar blastocyst stage. Embryos cultured from the 2-cell to the 4-cell stage were retarded by around 12 h when they reached the blastocyst stage. Developmental retardation was also reflected in the pattern of nutrient uptake, which lagged behind that of embryos developed in vivo. The present study has shown that it is possible to culture the early marsupial embryo to the blastocyst stage in a serum-free culture system, while concomitantly quantifying embryonic nutrient requirements. Such an approach is essential for species where there is a paucity of material for study.

Animals↗