scholarly journals CHANGING NUCLEAR HISTONE PATTERNS DURING DEVELOPMENT I. FERTILIZATION AND EARLY CLEAVAGE IN THE CRAB, EMERITA ANALOGA

1968 ◽  
Vol 16 (7) ◽  
pp. 473-479 ◽  
Author(s):  
JACK C. VAUGHN
Keyword(s):  
Developmental Stages ◽  
Sperm Nucleus ◽  
Bromphenol Blue ◽  
Early Cleavage ◽  
Fast Green ◽  
Adult Type ◽  
Emerita Analoga ◽  
Cleavage Stages ◽  
Nuclear Histone ◽  
Early Developmental

Application of cytochemical techniques to the early developmental stages of the decapod crab, Emerita analoga, shows the following. After fertilization, the sperm nucleus, which apparently contains no basic proteins prior to this stage, becomes associated with a class of weakly basic histones, which differ from adult type histones in their apparent inability to bind alkaline fast green and from protamines by their inability to bind bromphenol blue following acetylation. This class of histones only persists until the late pronucleus stage, by which time the chromosomes contain a class of histones that are indistinguishable from adult histones by qualitative cytochemical techniques. No further changes in the nuclear histones are detected in the zygote or early cleavage stages. These changing histone patterns during early crab development are discussed with reference to other similar studies in other organisms.

Maturation of the scolex syncytium in the metacestode ofHymenolepis diminuta, with special reference to microthrix formation

Parasitology ◽  
1984 ◽  
Vol 88 (2) ◽  
pp. 341-349 ◽  
Author(s):  
K. Sylvia Richards ◽  
C. Arme
Keyword(s):  
Developmental Stages ◽  
Apical Membrane ◽  
Final Host ◽  
Hymenolepis Diminuta ◽  
Bearing Surface ◽  
Adult Type ◽  
Asymmetric Membranes ◽  
Membrane Asymmetry ◽  
Outer Leaflet ◽  
Early Developmental

SUMMARYThe entire surface of the early developmental stages of the cysticercoid ofHymenolepis diminutabears microvilli. Posteriad differentiation produces a microthrix-bearing surface on the presumptive scolex region, commencing before scolex retraction in cysticercoids inTenebrio molitorkept at 26°C. During sucker development, the scolex syncytial cytoplasm possesses electron-dense discoidal bodies, aligned parallel to the surface. They become associated with the apical membrane, domes are formed and electron-dense spine-like profiles become apparent. Elevation on short shafts follows, and multilaminate baseplates are then discernible. Fewer microvilli are now present and vesicles with asymmetric membranes (denser inner leaflet) occur within the syncytial cytoplasm. Before scolex retraction, this differentiation extends to the level of the suckers; thus the neck, which becomes reflected on retraction, still possesses only microvilli. After retraction, differentiation proceeds rapidly with increased growth of existing microtriches, discoidal bodies possibly contributing to the shaft support material; the reflected neck develops microtriches and the microvilli are shed into the scolex retraction cavity. The ‘asymmetric’ vesicles increase numerically, some fusing with the apical membrane and releasing their contents. Concurrently, apical membrane asymmetry (denser outer leaflet) becomes apparent. The adult-type surface is formed by 3 days post-scolex retraction, coinciding with the earliest time that the metacestode is infective to the final host.

P–206 Does oocyte vitrifcation affect morphokinetics of subsequent embryo development?

2021 ◽  
Vol 36 (Supplement_1) ◽  
Author(s):  
S Montgomery ◽  
K Montgomery ◽  
D Nash ◽  
A Campbell
Keyword(s):  
Embryo Development ◽  
Live Birth ◽  
Developmental Stages ◽  
Controlled Trial ◽  
Implantation Rate ◽  
Clinical Pregnancy ◽  
Human Embryos ◽  
Early Cleavage ◽  
Oocyte Vitrification ◽  
Early Developmental

Abstract Study question Are the morphokinetic profiles, as assessed using time-lapse technology, of human embryos developed from vitrified oocytes different to those from fresh oocytes. Summary answer Vitrification of oocytes does have an effect on early developmental morphokinetic profiles, but this is normalized by the time the embryo has reached blastocyst. What is known already Vitrification of oocytes is now commonplace, but little is known about the effect this may have on subsequent embryo development. Study design, size, duration This was a retrospective data analysis, from 8 fertility clinics in the UK between 2012 and 2019. Embryos from patients in the vitrified group (n = 557) were matched to fresh patient controls (n = 539). The matching was performed based on the following criteria: type of treatment, patient age, cause of infertility and number of embryos. Participants/materials, setting, methods The embryos in each group were compared for mean morphokinetics of key developmental stages in hours post insemination (hpi). Parameters compared included early cleavage divisions (t2-t8), time to start of compaction (tSC), time to morula (tM), time to start blastulation (tSB), time to full blastocyst (tB) and duration of compaction (tB-tSC). Treatment outcomes were compared between the two groups, including percentage of blastocyst formation, clinical pregnancy rate, implantation rate and live birth rate. Main results and the role of chance The results showed a significant delay across all early cleavage divisions as follows for vitrified and fresh oocytes respectively: 2-cell (28.14 vs 26.10 (p < 0.001)), 3 cell (37.56 vs 35.37 (p < 0.001)), 4 cell (40.58 vs 37.54 (p < 0.001)), 5 cell (50.31 vs 47.14 (p < 0.001)), 6 cell (53.99 vs 50.87 (p < 0.001)), 7 cell (57.08 vs 54.48 (p < 0.001)) and 8 cell (61.26 vs 58.91 (p < 0.01)). In addition, tSC was also significantly delayed in the vitrified group (80.65 vs 76.36 (p < 0.001)). However, the compaction stage was significantly shorter in the vitrified oocytes (19.02 vs 22.45 (p < 0.001)). Therefore, there was no difference in the time that embryos derived from fresh and vitrified oocytes reached the blastocyst stage (108.03 vs 107.78 (p > 0.05)). No difference was found in clinical pregnancy, implantation or live birth rates but significantly fewer blastocyst developed from vitrified oocytes compared to fresh (36.09% vs 42.4% (p < 0.05)). Limitations, reasons for caution Although this was a matched analysis, it was a retrospective in nature therefore is subject to confounders. However, it would be problematic to perform a prospective randomized controlled trial to address this study question given the need to randomize patients to elective freezing of oocytes prior to embryo creation. Wider implications of the findings: Vitrification of oocytes may affect early developmental morphokinetic profiles, but any effect is normalized by the time the embryo has reached blastocyst. However, fewer blastocysts may develop following oocyte vitrification. This may have implications for oocyte donation banks and those patients choosing to cryopreserve oocytes. Trial registration number NA

scholarly journals CHANGES IN NUCLEAR HISTONES DURING FERTILIZATION, AND EARLY EMBRYONIC DEVELOPMENT IN THE PULMONATE SNAIL, Helix aspersa

1960 ◽  
Vol 8 (1) ◽  
pp. 69-81 ◽  
Author(s):  
David P. Bloch ◽  
Howard Y. C. Hew
Keyword(s):  
Developmental Stages ◽  
Picric Acid ◽  
Polar Body ◽  
Helix Aspersa ◽  
Bromphenol Blue ◽  
Fast Green ◽  
Specific Staining ◽  
Trichloracetic Acid ◽  
Basic Proteins ◽  
Snail Helix Aspersa

Calf thymus histories comprising two fractions, one rich in lysine, the other having roughly equal amounts of lysine and arginine, Loligo testes histones rich in arginine, and salmine, are compared with respect to their amino acid compositions, and their staining properties when the proteins are fixed on filter paper. The three types of basic proteins; somatic, arginine-rich spermatid histones, and protamine can be distinguished on the following basis. Somatic and testicular histones stain with fast green or bromphenol blue under the same conditions used for specific staining of histones in tissue preparations. The former histones lose most or all of their stainability after deamination or acetylation. Staining of the arginine-rich testicular histones remains relatively unaffected by this treatment. Protamines do not stain with fast green after treatment with hot trichloracetic acid, but are stained by bromphenol blue or eosin after treatment with picric acid. These methods provide a means for the characterization of nuclear basic proteins in situ. Their application to the early developmental stages of Helix aspersa show the following: After fertilization the protamine of the sperm is lost, and is replaced by faintly basic histones which differ from adult histones in their inability to bind fast green, and from protamines, by both their inability to bind eosin, and their weakly positive reaction with bromphenol blue. These "cleavage" histones are found in the male and female pronuclei, the early polar body chromosomes, and the nuclei of the cleaving egg and morula stages. During gastrulation, the histone complement reverts to a type as yet indistinguishable from that of adult somatic cells.

scholarly journals Cortical-nuclear interactions in cephalopod development: cytochalasin B effects on the informational pattern in the cell surface

Development ◽  
1974 ◽  
Vol 31 (1) ◽  
pp. 1-25
Author(s):  
John M. Arnold ◽  
Lois D. Williams-Arnold
Keyword(s):  
Cytochalasin B ◽  
Developmental Stages ◽  
Early Cleavage ◽  
Organ Differentiation ◽  
Asymmetrical Pattern ◽  
Clear Cytoplasm ◽  
Weak Surface ◽  
Loligo Pealei ◽  
Early Developmental ◽  
Low Dosage

Cytochalasin B (CB) was applied to early developmental stages of the egg of the squid Loligo pealei and defects in cleavage and/or organogenesis were produced. If CB was applied in relatively high dosages (2·0 μg/ml) or for long periods (30 min) to embryos in early cleavage the existing furrows irreversibly disappeared. If precleavage embryos were similarly treated the streaming pattern which forms the blastodisc was interrupted and patches of clear cytoplasm appeared on the zygote surface. Short low dosage pulses (0·2 μg/ml for 10 min) produced cleavage effects correlated with the time of pulsing. If pulsed within 30 min of first cleavage the first furrow did not appear in the majority of cases but the second furrow appeared synchronously with the controls and appeared normal in all respects. If pulsed approximately 30 min or longer before cleavage the first furrow usually appeared on time as a weak surface line. Second cleavage appeared normally. However, the asymmetrical pattern of third cleavage was ‘equalized’ and the blastomeres tended to be of equal size. It was concluded that there are subtle cytoplasmic movement patterns, sensitive to CB, which position the nuclei before each cleavage and thereby determine the cleavage pattern. If embryos were pulsed (0·2 μg/ml for 10 min) at various times during early development, anomalies in differentiation at organogenesis (3–4 days later) were produced which correlated with the time of pulsing. Pulses after germinal layer formation (stage 11) produced no noticeable effects and pulses before the cytoplasmic streaming which produces the blastodisc similarly had very little or no effect. However, pulses during blastodisc formation or early cleavage produced severely affected embryos in which organ displacement, poor tissue and organ differentiation, or organ deficiencies were common. Pulsed embryos were scored and the time of pulsing correlated with the severity of effects. The nuclei of the inductive yolk epithelium were abnormal, frequently being rounded, clumped and/or containing clumped or abnormally diffuse chromatin. It was concluded that the streaming pattern which forms the blastodisc in some way fixes or enhances a pre-existing pattern of developmental information which resides in or at the surface of the egg. Once this pattern is established it is insensitive to CB but it can still be demonstrated by other techniques. This informational pattern apparently influences the nuclei of the yolk epithelium that come to lie in specific regions and controls the expression of their genome so that specific organs are programmed.

Correlated Studies of Cellular Interactions Using TEM, Freeze Etching, and SEM

1974 ◽  
Vol 32 ◽  
pp. 320-321
Author(s):  
J. P. Revel
Keyword(s):  
Developmental Stages ◽  
Three Dimensional ◽  
Cell Movement ◽  
Cellular Interactions ◽  
Serial Sections ◽  
Cell Sheets ◽  
Freeze Etching ◽  
Early Developmental

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.

Review of early developmental stages of trilobites and agnostids from the Barrandian area (Czech Republic)

2017 ◽  
Vol 186 (1) ◽  
pp. 103-112
Author(s):  
Lukáš Laibl ◽  
Oldřich Fatka
Keyword(s):  
Czech Republic ◽  
Developmental Stages ◽  
History Of Research ◽  
Early Developmental Stages ◽  
History Of ◽  
Barrandian Area ◽  
Early Developmental

This contribution briefly summarizes the history of research, modes of preservation and stratigraphic distribution of 51 trilobite and five agnostid taxa from the Barrandian area, for which the early developmental stages have been described.

scholarly journals The Effect of an Anthropogenic Magnetic Field on the Early Developmental Stages of Fishes—A Review

2021 ◽  
Vol 22 (3) ◽  
pp. 1210
Author(s):  
Krzysztof Formicki ◽  
Agata Korzelecka-Orkisz ◽  
Adam Tański
Keyword(s):  
Magnetic Fields ◽  
Developmental Stages ◽  
Negative Influence ◽  
Pigment Cells ◽  
Egg Activation ◽  
Industrial Equipment ◽  
Positive Effects ◽  
Early Developmental Stages ◽  
Species Specific ◽  
Early Developmental

The number of sources of anthropogenic magnetic and electromagnetic fields generated by various underwater facilities, industrial equipment, and transferring devices in aquatic environment is increasing. These have an effect on an array of fish life processes, but especially the early developmental stages. The magnitude of these effects depends on field strength and time of exposure and is species-specific. We review studies on the effect of magnetic fields on the course of embryogenesis, with special reference to survival, the size of the embryos, embryonic motor function, changes in pigment cells, respiration hatching, and directional reactions. We also describe the effect of magnetic fields on sperm motility and egg activation. Magnetic fields can exert positive effects, as in the case of the considerable extension of sperm capability of activation, or have a negative influence in the form of a disturbance in heart rate or developmental instability in inner ear organs.

scholarly journals Wnt/β-catenin Pathway-Mediated PPARδ Expression during Embryonic Development Differentiation and Disease

2021 ◽  
Vol 22 (4) ◽  
pp. 1854
Author(s):  
Tabinda Sidrat ◽  
Zia-Ur Rehman ◽  
Myeong-Don Joo ◽  
Kyeong-Lim Lee ◽  
Il-Keun Kong
Keyword(s):  
Embryonic Development ◽  
Transcriptional Activation ◽  
Target Gene ◽  
Developmental Stages ◽  
Embryonic Stem ◽  
Hereditary Diseases ◽  
Peroxisome Proliferator ◽  
Peroxisome Proliferator Activated Receptor ◽  
Stem Cell Regulation ◽  
Early Developmental

The Wnt/β-catenin signaling pathway plays a crucial role in early embryonic development. Wnt/β-catenin signaling is a major regulator of cell proliferation and keeps embryonic stem cells (ESCs) in the pluripotent state. Dysregulation of Wnt signaling in the early developmental stages causes several hereditary diseases that lead to embryonic abnormalities. Several other signaling molecules are directly or indirectly activated in response to Wnt/β-catenin stimulation. The crosstalk of these signaling factors either synergizes or opposes the transcriptional activation of β-catenin/Tcf4-mediated target gene expression. Recently, the crosstalk between the peroxisome proliferator-activated receptor delta (PPARδ), which belongs to the steroid superfamily, and Wnt/β-catenin signaling has been reported to take place during several aspects of embryonic development. However, numerous questions need to be answered regarding the function and regulation of PPARδ in coordination with the Wnt/β-catenin pathway. Here, we have summarized the functional activation of the PPARδ in co-ordination with the Wnt/β-catenin pathway during the regulation of several aspects of embryonic development, stem cell regulation and maintenance, as well as during the progression of several metabolic disorders.

scholarly journals Mitochondrial Processes during Early Development of Dictyostelium discoideum: From Bioenergetic to Proteomic Studies

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 638
Author(s):  
Monika Mazur ◽  
Daria Wojciechowska ◽  
Ewa Sitkiewicz ◽  
Agata Malinowska ◽  
Bianka Świderska ◽  
...  
Keyword(s):  
Life Cycle ◽  
Developmental Stages ◽  
Coupling Efficiency ◽  
Slime Mold ◽  
Intact Cells ◽  
Life Cycle Stages ◽  
Early Developmental Stages ◽  
Proteomic Study ◽  
And Function ◽  
Early Developmental

The slime mold Dictyostelium discoideum’s life cycle includes different unicellular and multicellular stages that provide a convenient model for research concerning intracellular and intercellular mechanisms influencing mitochondria’s structure and function. We aim to determine the differences between the mitochondria isolated from the slime mold regarding its early developmental stages induced by starvation, namely the unicellular (U), aggregation (A) and streams (S) stages, at the bioenergetic and proteome levels. We measured the oxygen consumption of intact cells using the Clarke electrode and observed a distinct decrease in mitochondrial coupling capacity for stage S cells and a decrease in mitochondrial coupling efficiency for stage A and S cells. We also found changes in spare respiratory capacity. We performed a wide comparative proteomic study. During the transition from the unicellular stage to the multicellular stage, important proteomic differences occurred in stages A and S relating to the proteins of the main mitochondrial functional groups, showing characteristic tendencies that could be associated with their ongoing adaptation to starvation following cell reprogramming during the switch to gluconeogenesis. We suggest that the main mitochondrial processes are downregulated during the early developmental stages, although this needs to be verified by extending analogous studies to the next slime mold life cycle stages.

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