Cap Formation Research Articles

Enhanced mass transfer from the installation of a sieve tray subject to the variation of liquid heights and flow regimes in a bubble column

This work addressed the gas–liquid (G/L) mass transfer limitation coming from the increasing liquid height and the circumvention of the limitation by introducing a sieve tray in a bubble column. Either monoethylene glycol (MEG) solution or n-hexane was adopted as a liquid phase and argon was used as a gas phase in the bubble column. The gas holdup and the mass transfer coefficient became lowered by the static liquid height increase due to the increase of bubble size. The loss of mass transfer was overcome by installing a sieve tray inside the column. The two sieve trays with different hole sizes were employed and both bubble diameter and standard deviation of pressure were investigated to understand the effect of the sieve tray on the mass transfer. With a smaller size hole sieve (1mm), the mass transfer deteriorated in both liquid systems (MEG and n-hexane) due to the formation of gas cap below the sieve while with a larger hole sieve (3mm), it was enhanced because of the reduction of bubble diameters without any gas cap formation. However, it was found that the sieve tray effect was weakened when the flow regime changes from homogeneous to heterogeneous.

Amorphous Calcium Phosphate Formation and Aggregation Process Revealed by Light Scattering Techniques

Amorphous calcium phosphate (ACP) attracts attention as a precursor of crystalline calcium phosphates (CaPs) formation in vitro and in vivo as well as due to its excellent biological properties. Its formation can be considered to be an aggregation process. Although aggregation of ACP is of interest for both gaining a fundamental understanding of biominerals formation and in the synthesis of novel materials, it has still not been investigated in detail. In this work, the ACP aggregation was followed by two widely applied techniques suitable for following nanoparticles aggregation in general: dynamic light scattering (DLS) and laser diffraction (LD). In addition, the ACP formation was followed by potentiometric measurements and formed precipitates were characterized by Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), and atomic force microscopy (AFM). The results showed that aggregation of ACP particles is a process which from the earliest stages simultaneously takes place at wide length scales, from nanometers to micrometers, leading to a highly polydisperse precipitation system, with polydispersity and vol. % of larger aggregates increasing with concentration. Obtained results provide insight into developing a way of regulating ACP and consequently CaP formation by controlling aggregation on the scale of interest.

Rheology of simulated radioactive waste slurry and cold cap during vitrification

AbstractDuring the vitrification of radioactive waste in a Joule‐heated melter, aqueous melter feed slurry forms a cold cap, a reacting and melting material, which floats on the surface of the molten glass. The rheological behavior of the feed affects cold cap formation and shape, and is vital for modeling the feed‐to‐melt conversion process. We used slurry feed simulant and fast‐dried slurry solids representing the cold cap to investigate the rheological behavior of the feed as it transforms into glass. Both low‐temperature and high‐temperature rheometry were performed and a new scheme was applied to estimate the feed viscosity. This study shows that the conversion advances in four sequential stages that form distinct regions in the cold cap: (i) a fast‐spreading boiling slurry from which water evaporates, (ii) a porous solid region (viscosity > 108 Pa s) containing reacting solids and molten salts, (iii) a plastic region in which glass‐forming melt connects the refractory solids (~108 to ~106 Pa s), and (iv) a viscous foam layer in which the viscosity drops from ~105 to ~101 Pa s. The implications for the mathematical modeling of the cold cap are discussed.

DHX15 regulates CMTR1-dependent gene expression and cell proliferation

CMTR1 contributes to mRNA cap formation by methylating the first transcribed nucleotide ribose at the O-2 position. mRNA cap O-2 methylation has roles in mRNA stabilisation and translation, and self-RNA tolerance in innate immunity. We report that CMTR1 is recruited to serine-5-phosphorylated RNA Pol II C-terminal domain, early in transcription. We isolated CMTR1 in a complex with DHX15, an RNA helicase functioning in splicing and ribosome biogenesis, and characterised it as a regulator of CMTR1. When DHX15 is bound, CMTR1 activity is repressed and the methyl-transferase does not bind to RNA pol II. Conversely, CMTR1 activates DHX15 helicase activity, which is likely to impact several nuclear functions. In HCC1806 breast carcinoma cell line, the DHX15-CMTR1 interaction controls ribosome loading of a subset of mRNAs and regulates cell proliferation. The impact of the CMTR1-DHX15 interaction is complex and will depend on the relative expression of these enzymes and their interactors, and the cellular dependency on different RNA processing pathways.

Mesoscopic Energy Minimization Drives Pseudomonas aeruginosa Biofilm Morphologies and Consequent Stratification of Antibiotic Activity Based on Cell Metabolism.

ABSTRACTSegregation of bacteria based on their metabolic activities in biofilms plays an important role in the development of antibiotic resistance. Mushroom-shaped biofilm structures, which are reported for many bacteria, exhibit topographically varying levels of multiple drug resistance from the cap of the mushroom to its stalk. Understanding the dynamics behind the formation of such structures can aid in design of drug delivery systems, antibiotics, or physical systems for removal of biofilms. We explored the development of metabolically heterogeneous Pseudomonas aeruginosa biofilms using numerical models and laboratory knockout experiments on wild-type and chemotaxis-deficient mutants. We show that chemotactic processes dominate the transformation of slender and hemispherical structures into mushroom structures with a signature cap. Cellular Potts model simulation and experimental data provide evidence that accelerated movement of bacteria along the periphery of the biofilm, due to nutrient cues, results in the formation of mushroom structures and bacterial segregation. Multidrug resistance of bacteria is one of the most threatening dangers to public health. Understanding the mechanisms of the development of mushroom-shaped biofilms helps to identify the multidrug-resistant regions. We decoded the dynamics of the structural evolution of bacterial biofilms and the physics behind the formation of biofilm structures as well as the biological triggers that produce them. Combining in vitro gene knockout experiments with in silico models showed that chemotactic motility is one of the main driving forces for the formation of stalks and caps. Our results provide physicists and biologists with a new perspective on biofilm removal and eradication strategies.

Pliocene and Pleistocene chronostratigraphy of continental sediments underlying the Altiplano at La Paz, Bolivia

Continental sediments underlying the Altiplano plateau provide insight into the late Cenozoic evolution of the Central Andes. We characterize the magnetostratigraphy and lithostratigraphy of the upper part of this fill sequence along a transect extending southwestward from the Cordillera Real at La Paz, Bolivia, where it is best exposed. Multiple polarity reversals and the locally extensive, 2.74-Ma Chijini Tuff enable correlation between our six sections and three previously reported sections. The tuff ties the composite polarity sequence to the geomagnetic polarity time scale, demonstrating that the stratigraphic record extends from the latest Gilbert Chron (ca. 3.8 Ma) to the late Olduvai subchron (ca. 1.8 Ma), or possibly Jaramillo subchron (ca. 1.0 Ma). The sequence provides Earth's longest known record of low-latitude glaciation and the only record of Pliocene tropical glaciation. It includes evidence for 16 late Pliocene and Early Pleistocene glaciations, separated by interglacials of sufficient length (>103-104 a) to produce mature soil profiles. Successively larger ice caps formed directly before, during, and after the globally warm mid-Piacenzian (3.265–3.025 Ma), and throughout Plio-Pleistocene climate deterioration. The late Pliocene glacial units predate the onset of widespread Northern Hemisphere continental glaciation and in most cases unambiguously correspond to specific cool peaks of the astronomically tuned, benthic oxygen isotope (δ18O) record, including marine isotope stages MG2, M2, KM2, and G10. The glacial events broadly coincide with those nearer both poles, suggesting inter-hemispheric climate linkages. The early formation and subsequent expansion of ice caps beyond glacier margins of the Last Glacial Maximum suggest that the Cordillera Real likely attained its modern height before ca. 3.4 Ma. The number and timing of glaciations, and long-term sediment accumulation and incision rates suggest that the local Altiplano surface formed by ca. 1.8 Ma, after which headwaters of the Amazon River system breached the Cordillera Real and began to incise the fill sequence. The sequence spans at least 2 Ma before and during the first main pulses of the Great American Biotic Interchange, providing an important record of faunal migration. The arrival of savanna-adapted North American mammals in the Central Andes during this period points to the influence of glaciation on faunal migration in the southern tropics, similar to influences proposed in North and Central America.

Identification of small molecule inhibitors of the Chikungunya virus nsP1 RNA capping enzyme

Chikungunya virus (CHIKV) is an arthropod-borne alphavirus. Alphaviruses are positive strand RNA viruses that require a 5′ cap structure to direct translation of the viral polyprotein and prevent degradation of the viral RNA genome by host cell nucleases. Formation of the 5′ RNA cap is orchestrated by the viral protein nsP1, which binds GTP and provides the N-7 methyltransferase and guanylyltransferase activities that are necessary for cap formation. Viruses with aberrant nsP1 activity are unable to replicate effectively suggesting that nsP1 is a promising target for antiviral drug discovery. Given the absence of commercially available antiviral therapies for CHIKV, it is imperative to identify compounds that could be developed as potential therapeutics. This study details a high-throughput screen of 3051 compounds from libraries containing FDA-approved drugs, natural products, and known bioactives against CHIKV nsP1 using a fluorescence polarization-based GTP competition assay. Several small molecule hits from this screen were able to compete with GTP for the CHIKV nsP1 GTP binding site at low molar concentrations. Compounds were also evaluated with an orthogonal assay that measured the ability of nsP1 to perform the guanylation step of the capping reaction in the presence of inhibitor. In addition, live virus assays with CHIKV and closely related alphavirus, Sindbis virus, were used in conjunction with cell toxicity assays to determine the antiviral activity of compounds in cell culture. The naturally derived compound lobaric acid was found to inhibit CHIKV nsP1 GTP binding and guanylation as well as attenuate viral growth in vitro at both 24 hpi and 48 hpi in hamster BHK21 and human Huh 7 cell lines. These data indicate that development of lobaric acid and further exploration of CHIKV nsP1 as a drug target may aid in the progress of anti-alphaviral drug development strategies.

Growth Analysis of Single-Walled Carbon Nanotubes Based on Interatomic Potentials by Molecular Dynamics Simulation

Molecular dynamics simulation was performed to understand the growth mechanism of single-walled carbon nanotubes (SWNTs) by using the Brenner–Tersoff potential as the interaction among carbon atoms (C–C) and the Tersoff-type potential as the interaction between carbon and metal (C–M) and between metal and metal atoms (M–M). The potential functions for C–M and M–M bonds were established from the results of ab initio calculations. The growth of high-quality SWNTs was simulated at a suitable temperature and supply ratio of carbon atoms. The potential energy of carbon atoms was strongly dependent on the number of C–C and C–M bonds. The dependence explains the growth process, including cap formation, its lift-off, and the continuous SWNT growth.

Synthesis and Physico-Chemical Characterization of Different Mesoporous Bioactive Glass Nanopowders: in-vitro SBF Activity and Cytotoxicity

ABSTRACTMesoporous bioactive glass (MBG) nanopowders from SiO2-CaO-P2O5 system have been prepared by three different variations using different structure directing agents: (1) through wet chemical method (MBWC650) using non-ionic surfactant, PEG; (2) using Pluronic P123, another non-ionic surfactant via hydrothermal process (MBHM650); and (3) using ionic surfactant CTAB, via wet chemical process (MBCTAB650). Comparative study of phase, morphology and textural properties of all M BG nanopowders were accomplished by different characterization techniques. Specific surface area of powders was found to be 52.2, 169.3 and 473.2 m2.g–1 for MBWC650, MBHM650 and MBCTAB650, respectively. Kinetic SBF immersion study was carried out to examine hydroxyapatite forming ability of the powders. Supernatant analyses showed high dissolution of Ca2+ and PO43– ions in MBCTAB650 while MBHM650 showed initial level of HAp formation ability over its surface in contrast with MBWC650. Other characterizations confirmed formation of Ca-P over MBG nanopowders. Cell viability of 117% for MBWC650, 90% for MBHM650 and 89% for MBCTAB650 after seven days were noted. MBHM650 and MBWC650 could be suitable candidate as dental/orthopedic bone filler material whereas high surface area of MBCTAB650 powder can be useful for delivering pharmaceutical agents in-vitro / in-vivo.

Sodium fluoride disturbs DNA methylation of NNAT and declines oocyte quality by impairing glucose transport in porcine oocytes.

Sodium fluoride (NaF) is used as a medicine to prevent tooth decay; however, excessive NaF could cause a pathological damage to the health. Recent studies showed that NaF impaired mouse oocyte maturation, included of abnormal spindle configuration, actin cap formation, cortical granule-free domain formation, and the following development after fertilization. However, few studies used large animals as models to study the toxicology of NaF on oocytes maturation. We proposed a hypothesis that NaF would affect the nuclear and cytoplasmic maturation of porcine oocytes and DNA methylation pattern of imprinted genes in oocytes. Our results showed that NaF affected cumulus expansion, polar body emission, spindle morphology, cortical granule distribution, early apoptosis, and the following development after parthenogenetic activation during porcine oocyte maturation. Moreover, NaF increased the DNA methylation of NNAT and decreased its expression, which disturbed the glucose transport in oocytes. These results suggest that NaF impairs the porcine oocytes maturation epigenetically, which provides a new toxicological mechanism of NaF on the oocyte maturation. Environ. Mol. Mutagen. 59:223-233, 2018. © 2017 Wiley Periodicals, Inc.

A transgenic reporter under control of an es1 promoter/enhancer marks wound epidermis and apical epithelial cap during tail regeneration in Xenopus laevis tadpole

Rapid wound healing and subsequent formation of the apical epithelial cap (AEC) are believed to be required for successful appendage regeneration in amphibians. Despite the significant role of AEC in limb regeneration, its role in tail regeneration and the mechanisms that regulate the wound healing and AEC formation are not well understood. We previously identified Xenopus laevis es1, which is preferentially expressed in wounded regions, including the AEC after tail regeneration. In this study we established and characterized transgenic Xenopus laevis lines harboring the enhanced green fluorescent protein (EGFP) gene under control of an es1 gene regulatory sequence (es1:egfp).The EGFP reporter expression was clearly seen in several regions of the embryo and then declined to an undetectable level in larvae, recapitulating the endogenous es1 expression. After amputation of the tadpole tail, EGFP expression was re-activated at the edge of the stump epidermis and then increased in the wound epidermis (WE) covering the amputation surface. As the stump started to regenerate, the EGFP expression became restricted to the most distal epidermal region, including the AEC. EGFP was preferentially expressed in the basal or deep cells but not in the superficial cells of the WE and AEC.We performed a small-scale pharmacological screening for chemicals that affected the expression of EGFP in the stump epidermis after tail amputation. The EGFP expression was attenuated by treatment with an inhibitor for ERK, TGF-β or reactive oxygen species (ROS) signaling. These treatments also impaired wound closure of the amputation surface, suggesting that the three signaling activities are required for es1 expression in the WE and successful wound healing after tail amputation.These findings showed that es1:egfp Xenopus laevis should be a useful tool to analyze molecular mechanisms regulating wound healing and appendage regeneration.

Phosphorus dynamics in and below the redoxcline in the Black Sea and implications for phosphorus burial

Marine basins with oxygen-depleted deep waters provide a natural laboratory to investigate the consequences of anoxic and sulfidic (i.e. euxinic) conditions for biogeochemical processes in seawater and sediments. In this study, we investigate the dynamics of the key nutrient phosphorus (P) and associated elements such as manganese (Mn), iron (Fe) and calcium (Ca) in the euxinic deep basin of the Black Sea. By examining water column particles with scanning electron microscope – energy dispersive spectroscopy and synchrotron-based X-ray absorption spectroscopy, we show that Mn(III/IV)-P is the key form of particulate P in the redoxcline. Other forms of particulate P include organic P, Fe(III)-P, and inorganic polyphosphates. Most inorganic P particles that are formed in the redoxcline subsequently dissolve in the underlying sulfidic waters, with the exception of some particulate Fe(III)-P that accounts for <1% of all P settling onto the seafloor. Organic P is the dominant source of P to the sediment. Most of this organic P is degraded in the upper 2 cm of the sediment. Results of sequential extractions and a 33P radiotracer experiment point towards the formation of labile Ca-P and P adsorbed onto calcium-carbonate and clays and a role of these phases as a major sink of P in the sediment. The total P burial efficiency in the sediments is ∼27%, which is relatively high when compared to estimates for sediments in other euxinic basins such as the Baltic Sea (<12%). We suggest that the abundant presence of calcium carbonate may contribute to the more efficient sequestration of P in Black Sea sediments.

Experiments on the transition of fast to slow bubbles in water

Bubbles have two levels of rise velocity in water called fast and slow. The fast ones are associated with a mobile interface while the slow ones are considered immobile like spheres. Whenever fast bubbles are generated they transfer to slow ones by accumulation of impurities present in the water. In this work we investigate this transfer with a rotary chamber technique. The technique allows the levitation and continuous observation of a bubble on its way from fast to slow. We used standard distilled water conforming to DIN 43530 and VDE 0510 with a specific conductance <10μS/cm. It led to long transfer periods of up to 45min. The analysis of the bubble trajectory provided the histories of drag, lift and shape. The overall results support the cap formation theory.

Chromosome Healing Is Promoted by the Telomere Cap Component Hiphop in Drosophila.

The addition of a new telomere onto a chromosome break, a process termed healing, has been studied extensively in organisms that utilize telomerase to maintain their telomeres. In comparison, relatively little is known about how new telomeres are constructed on broken chromosomes in organisms that do not use telomerase. Chromosome healing was studied in somatic and germline cells of Drosophila melanogaster, a nontelomerase species. We observed, for the first time, that broken chromosomes can be healed in somatic cells. In addition, overexpression of the telomere cap component Hiphop increased the survival of somatic cells with broken chromosomes, while the cap component HP1 did not, and overexpression of the cap protein HOAP decreased their survival. In the male germline, Hiphop overexpression greatly increased the transmission of healed chromosomes. These results indicate that Hiphop can stimulate healing of a chromosome break. We suggest that this reflects a unique function of Hiphop: it is capable of seeding formation of a new telomeric cap on a chromosome end that lacks a telomere.

Intersectin 2 controls actin cap formation and meiotic division in mouse oocytes through the Cdc42 pathway.

Intersectins (ITSNs), an evolutionarily conserved adaptor protein family, have been implicated in multiple biologic processes; however, their functions in mammalian oocytes have not been addressed. Here, we report delayed meiotic resumption and defective cytokinesis upon specific depletion of ITSN2 in mouse oocytes. In particular, abnormal spindle, misaligned chromosomes, and loss of cortical actin cap are readily observed in ITSN2-depleted oocytes. Similarly, a small molecule that targets the Cdc42-ITSN interaction also disrupts oocyte maturation and actin polymerization. Moreover, we find that ITSN2 depletion reduces the activity of Cdc42 in oocytes and, of note, that forced expression of the dominant-positive mutant of Cdc42, in part, prevents the effects of ITSN2 knockdown on actin cap formation. In addition, the localization of WASP and Arp2, the downstream effector proteins of Cdc42, is altered in ITSN2-depleted oocytes accordingly. In summary, our data support a model in which ITSN2 depletion induces the inactivation of Cdc42, which, in turn, influences the distribution and function of Arp2/3 and WASP, consequently disrupting oocyte polarity establishment and meiotic division.-Zhang, J., Ma, R., Li, L., Wang, L., Hou, X., Han, L., Ge, J., Li, M., Wang, Q. Intersectin 2 controls actin cap formation and meiotic division in mouse oocytes through the Cdc42 pathway.

The nuclear mitotic apparatus protein NuMA controls rDNA transcription and mediates the nucleolar stress response in a p53-independent manner.

The nuclear mitotic apparatus protein, NuMA, is involved in major cellular events such as DNA damage response, apoptosis and p53-mediated growth-arrest, all of which are under the control of the nucleolus upon stress. Proteomic investigation has identified NuMA among hundreds of nucleolar proteins. Yet, the precise link between NuMA and nucleolar function remains undetermined. We confirm that NuMA is present in the nucleolus and reveal redistribution of NuMA upon actinomycin D or doxorubicin-induced nucleolar stress. NuMA coimmunoprecipitates with RNA polymerase I, with ribosomal proteins RPL26 and RPL24, and with components of B-WICH, an ATP-dependent chromatin remodeling complex associated with rDNA transcription. NuMA also binds to 18S and 28S rRNAs and localizes to rDNA promoter regions. Downregulation of NuMA expression triggers nucleolar stress, as shown by decreased nascent pre-rRNA synthesis, fibrillarin perinucleolar cap formation and upregulation of p27kip1, but not p53. Physiologically relevant nucleolar stress induction with reactive oxygen species reaffirms a p53-independent p27kip1 response pathway and leads to nascent pre-rRNA reduction. It also promotes the decrease in the amount of NuMA. This previously uncharacterized function of NuMA in rDNA transcription and p53-independent nucleolar stress response supports a central role for this nuclear structural protein in cellular homeostasis.

Nanopatterned epitaxy of non-polar Ga1-yInyN layers with caps and voids

Low-defect density non-polar a-plane Ga1-yInyN layers on r-plane sapphire substrates are reported by implementing self-assembling nanopatterning in metalorganic vapor phase epitaxy. Nanopillar capping and void formation in regrowth lead to a 90% defect reduction. An ex-situ Ni layer transforms into a nanoisland etch mask to pattern GaN templates. a-Plane GaN and Ga1-yInyN layers with an InN content in the range of y = 0.04–0.11 are then regrown. Both exhibit a low density of basal-plane stacking faults of (4.6 ± 1.3) × 104 cm−1 by transmission electron microscopy analysis. Growth parameters and the template pattern are discussed by help of an X-ray rocking curve analysis. We find pattern the fill factor and V/III ratio to dominate the defect reduction. Resulting layers should enable efficient long-wavelength light-emitting and solar cell devices.

Histone deacetylase 6 (HDAC6) is an essential factor for oocyte maturation and asymmetric division in mice

Tubastatin A (Tub-A), a highly selective histone deacetylase 6 (HDAC6) inhibitor, has been widely used as a cytotoxic anticancer agent, or for the treatment of patients with asthma. However, the potential toxicity of Tub-A on oocyte maturation and asymmetric division is still unclear. Therefore, the present study was designed to examine the effect and potential regulatory role of Tub-A on the meiotic maturation of oocytes. We observed that Tub-A treatment induced an increased level of the acetylation of α-tubulin, and a failure of spindle migration and actin cap formation. Based on the spindle structure, most Tub-A treated oocytes were arrested in an MI-like or a GVBD-like stage and exhibited decondensed chromosomes in a dose dependent manner. Moreover, Tub-A treatment decreased the protein expression of mTOR, a factor responsible for spindle formation, and the expression of mDia1, an inhibitor of actin assembly, in an HDAC6 expression-dependent manner. Importantly, following Tub-A supplementation, most oocytes failed to extrude the first polar body, which indicates that these defects are closely linked to abnormal oocyte maturation. Taken together, our data demonstrates that HDAC6 is one of the essential factors for oocyte maturation and asymmetric division via the HDAC6/mTOR or mDia1 pathway in mice.

Biomimetic in situ nucleation of calcium phosphates by protein immobilization on high strength ceramic materials

Zirconia has been commonly used in the dental industry because of its excellent biological, mechanical and aesthetic properties. This material, however, is classified as nearly inert. To bioactivate the ceramic surface, biomimetic depositions of calcium phosphate coatings have been developed. We demonstrate an accelerated biomimetic coating method on zirconia using a specific pre-treatment with biological agents. We have chosen bovine serum albumin as a standard protein. Through the pre-treatment of the zirconia using a hydroxylation or additionally immobilizing the bovine serum albumin on the surface, we could influence the CaP deposition rate. Immunohistochemical analyses verified the presence of BSA on the zirconia surfaces. After immersion in simulated body fluid at 40°C, the samples were analyzed by scanning electron microscopy and X-ray diffraction to visualize the CaP formation. Here we could show as proof-of-principle that it is possible to accelerate biomimetic coating processes on zirconia implants containing BSA on their surface.

JAK2 inhibitor CEP-33779 prevents mouse oocyte maturation in vitro.

The inhibitor CEP-33779 is a specific selective inhibitor of Janus kinase 2 (JAK2). In most somatic cells, JAK2 plays essential roles in cellular signal transduction and in the regulation of cell cycle. Little is known regarding the effects of JAK2 on mammalian oocyte maturation. In the present study, we investigated the effects of CEP-33779 on mouse oocytes’ meiosis and the possible mechanisms of JAK2 during mouse oocyte maturation. We detected the distribution of JAK2 during the mouse oocyte maturation. The results showed that JAK2 was mainly distributed in the cytoplasm during maturation. We cultured mouse oocytes with CEP-33779, examined the maturation rate, spindle morphology, and organization of microfilaments during the mouse oocyte maturation. While the rate of germinal vesicle breakdown (GVBD) did not differ between the treated and control groups, the rate of oocyte maturation decreased significantly when treated with CEP-33779. The rate of maturation was 21.14% in treated group and was 81.44% in control group. The results show that CEP-33779 inhibits the maturation of mouse oocytes. There was no obvious difference in the meiotic spindle morphology between the treated and control groups. The results show that CEP-33779 treatment did not disrupt the reorganization of microtubules. The microfilament observation shows that the microfilament did not form actin cap and the spindle stayed at the center of the oocyte in the treated group. CEP-33779 treatment inhibited the maturation of mouse oocytes which might be because of the disruption of formation of the actin cap. These results suggest that JAK2 regulated the microfilaments aggregation during the mouse oocyte maturation.