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Park, Yeo-Reum,Park, Hye-Bin,Kim, Mi-Jeong,Jung, Bae-Dong,Lee, Seunghyung,Park, Choon-Keun,Cheong, Hee-Tae The Korean Society of Developmental Biology 2019 발생과 생식 Vol.23 No.1
We examined the effects of endoplasmic reticulum (ER) stress inhibitor treatment during the micromanipulation of porcine somatic cell nuclear transfer (SCNT) on the in vitro development of SCNT embryos. ER stress inhibitors such as salubrinal (200 nM) and tauroursodeoxycholic acid (TUDCA; $100{\mu}M$) were added to the micromanipulation medium and holding medium. The expression of X-box binding protein 1 (Xbp1), ER-stress-associated genes, and apoptotic genes in SCNT embryos was confirmed at the one-cell and blastocyst stages. Levels of Xbp1 splicing and expression of ER-stress-associated genes in SCNT embryos at the one-cell stage decreased significantly with TUDCA treatment (p<0.05). The expression of ER-stress-associated genes also decreased slightly with the addition of both salubrinal and TUDCA (Sal+TUD). The expression levels of caspase-3 and Bcl2-associated X protein (Bax) mRNA were also significantly lower in the TUDCA and Sal+TUD treatments (p<0.05). At the blastocyst stage, there were no differences in levels of Xbp1 splicing, and transcription of ER-stress-associated genes and apoptosis genes between control and treatment groups. However, the blastocyst formation rate (20.2%) and mean blastocyst cell number ($63.0{\pm}7.2$) were significantly higher (p<0.05) for embryos in the TUDCA treatment compared with those for control (12.6% and $41.7{\pm}3.1$, respectively). These results indicate that the addition of ER-stress inhibitors, especially TUDCA, during micromanipulation can inhibit cellular damage and enhance in vitro development of SCNT embryos by reducing stress levels in the ER.
Park, A Reum,Kim, Jung Sub,Kim, Kwang Su,Zhang, Kan,Park, Juhyun,Park, Jong Hyeok,Lee, Joong Kee,Yoo, Pil J. American Chemical Society 2014 ACS APPLIED MATERIALS & INTERFACES Vol.6 No.3
<P>Although Si is a promising high-capacity anode material for Li-ion batteries (LIB), it suffers from capacity fading due to excessively large volumetric changes upon Li insertion. Nanocarbon materials have been used to enhance the cyclic stability of LIB anodes, but they have an inherently low specific capacity. To address these issues, we present a novel ternary nanocomposite of Si, Mn, and reduced graphene oxide (rGO) for LIB anodes, in which the Si–Mn alloy offers high capacity characteristics and embedded rGO nanosheets confer structural stability. Si–Mn/rGO ternary nanocomposites were synthesized by mechanical complexation and subsequent thermal reduction of mixtures of Si nanoparticles, MnO<SUB>2</SUB> nanorods, and rGO nanosheets. Resulting ternary nanocomposite anodes displayed a specific capacity of 600 mAh/g with ∼90% capacity retention after 50 cycles at a current density of 100 mA/g. The enhanced performance is attributed to facilitated Li-ion reactions with the MnSi alloy phase and the formation of a structurally reinforced electroconductive matrix of rGO nanosheets. The ternary nanocomposite design paradigm presented in this study can be exploited for the development of high-capacity and long-life anode materials for versatile LIB applications.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/aamick/2014/aamick.2014.6.issue-3/am404608d/production/images/medium/am-2013-04608d_0008.gif'></P>
Yeo-Reum Park,Hye-Bin Park,Hwa-Yeon Lee,Hyo-Kyung Bae,Hui-Yeon Shin,Seunghyung Lee,Choon-Keun Park,Boo-Keun Yang,Hee-Tae Cheong 한국수정란이식학회 2016 한국수정란이식학회 학술대회 Vol.2016 No.10
This study was conducted to examine the effects of activation methods on the ER stress induction and subsequent apoptosis and in vitro development of porcine parthenogenetic embryos. Porcine in vitro matured oocytes were activated by four activation methods; 1) electric stimulus(ES) with two DC pulses of 1.25 kV/cm, for 30 ㎲ (E), 2) ES + 10 μM Ca-ionophore (A23187) treatment for 5 min (EC), 3) ES + 2 mM 6-dimethylaminopurine treatment for 3 h (ED), or 4) ES + A23187 + 6-DMAP (ECD). After activation, parthenogenetic embryos were in vitro cultured in PZM-3 medium and sampled to analyze the x-box binding protein 1 (Xbp1) mRNA, ER stress-associated genes and apoptotic genes at 3 h post ES and the 1-cell and blastocyst stages. The un-spliced and spliced x-box binding protein 1 (Xbp1) mRNA were confirmed by RT-PCR. Also ER stress-associated genes, such as the C/EBP homologous protein (CHOP), binding protein (BiP), activating transcription factor 4 (ATF4) and glucose-regulated protein 94 (GRP94), and apoptotic genes were analyzed by real-time quantitative RT-PCR (RT-qPCR). The band intensities of spliced Xbp1 (Xbp1s) mRNA was higher in the EC group than other three groups at 3 h and the 1-cell stage, while it was higher in the ED groups compared with E group at the blastocyst stage. Four ER stress-associated genes were showed the highest expression in the EC group and weakly expressed in the ED group at 3 h. However, most of those genes were highly expressed in EC and ECD groups at the 1-cell and blastocyst stages with some variation. The expressions of Bcl-2-associated X protein (Bax) and caspase-3 mRNAs were significantly higher in EC group than other three groups at all stages. The developmental rate to the blastocyst stage was higher (p<0.05) in ED and ECD groups (32.1±3.8 to 34.6±2.2%) than that of E group (26.1±3.9%). These results suggest that the intracellular ER stress of parthenogenetic porcine embryos is affected by activation method and subsequently lead to the apoptosis of embryos.
Park, A Reum,Nam, Myeong Gyun,Kim, A-Young,Kim, Kwang Su,Sher Shah, Md. Selim Arif,Lee, Jun Young,Kim, Woo-Jae,Lee, Joong Kee,Yoo, Pil J. Elsevier 2017 Journal of Alloys and Compounds Vol.724 No.-
<P><B>Abstract</B></P> <P>Silicon (Si) is a promising anode material for high-performance Li-ion batteries (LIBs), but it undergoes rapid capacity fading through severe volumetric expansion during Li insertion/extraction. Although alloying Si with various metal sources has been pursued to mitigate the structural deterioration, the resulting materials have shown the intrinsic problem of low electrical conductivity. To address this conflicting issue, here we describe a novel ternary nanocomposite of Si/Co-CoSi<SUB>2</SUB>/reduced graphene oxide (rGO) made using a facile process of mechanical mixing of Si nanoparticles, Co<SUB>3</SUB>O<SUB>4</SUB> microparticles, and rGO nanosheets, followed by carbothermal reduction. Specifically, rGO, which has high electrical conductivity and structural integrity, could work as both a conductive matrix and a reducing agent in forming the Co-CoSi<SUB>2</SUB> phase inside the Si domains during thermal treatment. The proposed ternary nanocomposites exhibited a noteworthy specific capacity of 952 mA h g<SUP>−1</SUP> with 79.3% capacity retention after 80 cycles at a current density of 100 mA g<SUP>−1</SUP>. We attribute the improved electrochemical performance to the increased structural stability offered by the Co-CoSi<SUB>2</SUB> phase and the interconnected conductive framework of the rGO nanosheets. Therefore, we expect our design process for Si/Co-CoSi<SUB>2</SUB>/rGO ternary nanocomposites to be applicable to other materials that can eventually be used as high-performance anodes for the next generation LIBs.</P> <P><B>Highlights</B></P> <P> <UL> <LI> A new Si/Co-CoSi<SUB>2</SUB>/rGO ternary nanocomposite is suggested as Li-ion battery anodes. </LI> <LI> An electroconductive yet Li-inactive phase of Co-CoSi<SUB>2</SUB> is incorporated into a Si matrix. </LI> <LI> Encompassing rGO nanosheets provide mechanical stability and conductivity during cycles. </LI> <LI> Ternary nanocomposite exhibits excellent electrochemical performance. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development
Park, Mi‐,Ryung,Lee, Ah‐,Reum,Bui, Hong‐,Thuy,Park, Chankyu,Park, Keun‐,Kyu,Cho, Ssang‐,Goo,Song, Hyuk,Kim, Jae‐,Hwan,Van Thuan, Nguyen,Kim, Jin‐,Hoi Wiley‐Liss, Inc. 2011 Developmental dynamics Vol.240 No.7
<P><B>Abstract</B></P><P>Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two‐cell embryos were fused and cultured in vitro in Chatot‐Ziomek‐Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8–10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12–14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm. Developmental Dynamics 240:1660–1669, 2011. © 2011 Wiley‐Liss, Inc.</P>
Park, Yoorim,Jung, Min Kyung,Yoon, Sun Young,Lee, Ha-Reum,Hur, Dae Young,Kim, Daejin,Yang, Yoolhee,Kim, Tae Sung,Kim, Seonghan,Yoon, Suk Ran,Park, Hyun Jeong,Bang, Sa Ik,Cho, Dae Ho Published for the International Union of Biochemis 2013 Biotechnology and applied biochemistry Vol.60 No.3
<P>Adipose stem cells (ASCs) are pluripotent cells that can generate pure fat tissue for regeneration. Differentiated adipose cells have been generated by a common inducer cocktail composed of dexamethasone, insulin, and isobutylmethylxanthine (DIM). The major drawbacks of adipose cells are their tendency to float on the culture media and their cost. To overcome some of these disadvantages, a new inducer cocktail that includes insulin, dehydroepiandrosterone, and histamine (DH IH) was tested. As a result, lipid accumulation was elevated more than twofold with DH IH than with DIM. Cell adhesion and viability, which are important factors for stable differentiation, were increased with DH IH and were proven through measurement of mRNA expression levels of adhesion marker genes, N-cadherin and vascular cell adhesion molecule, as well as through an alamar blue assay. The expression of adipogenesis-related genes, adiponectin, and glucose transporter type 4 lasted for a long time. To improve the efficiency of grafting, cell adhesion and neovascularization need to be increased. Neovascularization was observed around the transplanted adipose cells, which showed a higher number of vessel formation in DH IH than in DIM. The above results suggest that DH IH can produce pure differentiated adipose cells effectively and enhance their adhesion onto the target location when these differentiated adipose cells were applied as a clinical resource.</P>
Park, Hye-Bin,Park, Yeo-Reum,Lee, Hwa-Yeon,Bae, Hyo-Kyung,Lee, Seunghyung,Park, Choon-Keun,Yang, Boo-Keun,Cheong, Hee-Tae The Korean Society of Embryo Transfer 2017 한국동물생명공학회지 Vol.32 No.1
This study was conducted to investigate the effect of activation method on the endoplasmic reticulum (ER) stress induction, apoptosis and in vitro development of porcine parthenogenetic embryos. Porcine in vitro matured oocytes were activated by four activation methods; 1) electric stimulus (ES) (E), 2) $ES+10{\mu}M$ Ca-ionophore (A23187) treatment (EC), 3) ES+2 mM 6-dimethylaminopurine (6-DMAP) treatment (ED), or 4) ES+A23187 and 6-DMAP treatments (ECD). Parthenogenetic embryos were sampled to analyze x-box binding protein 1 (Xbp1) mRNA, ER stress-associated genes and apoptosis genes at 3 h after ES and the 1-cell and blastocyst stages. In the EC group, the band intensity of spliced Xbp1 (Xbp1s) mRNA was higher than those of the other groups at the 3 h and 1-cell stage, and higher than that of the E group at the blastocyst stage. Four ER stress-associated genes were expressed at the highest level in the EC group and weakly expressed in the ED group at 3 h after activation. However, most of the genes were highly expressed at the 1-cell and blastocyst stages with some variation in the EC and ECD groups. Expression of Bcl-2-associated X protein (Bax) and caspase-3 mRNA was significantly higher in the EC group than in the other groups at all development stages. The developmental rates to the blastocyst stage were higher in the ED and ECD groups than in the E and EC groups. These results suggest that the intracellular ER stress of parthenogenetic porcine embryos is affected by the activation method and subsequently lead to the apoptosis of embryos.