• Title/Summary/Keyword: CHO-K1 cell

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Antioxidative Effects of Delphinidin under in vitro and Cellular System

  • Noh, Jeong-Sook;Cho, Yun-Ju;Kim, Boh-Kyung;Park, Kun-Young;Cho, Eun-Ju
    • Food Science and Biotechnology
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    • v.18 no.1
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    • pp.167-171
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    • 2009
  • This study examined the antioxidative activity of delphinidin, a kind of anthocyanidin from eggplant. Cellular protective potential from oxidative damage by nitric oxide (NO), superoxide anion ($O_2^-$), and peroxynitrite ($ONOO^-$) using epithelial cell line LLC-PK1 cell as well as in vitro radical scavenging effects were investigated. Delphinidin showed strong in vitro radical scavenging effects against NO, $O_2^-$, and hydroxyl radical (${\cdot}OH$) in dose-dependent manners. In addition, delphinidin increased cell viability in LLC-PK1 cells in a concentration-dependent manner when viability was reduced by $ONOO^-$-induced oxidative damage. To elucidate the protective mechanisms of delphinidin from $ONOO^-$, sodium nitroprusside (SNP), and pyrogallol were also employed to generate NO and $O_2^-$, respectively. The treatment of delphinidin recovered reductions in cell viability caused by SNP and pyrogallol, indicating that delphinidin can attenuate oxidative stress induced by NO and $O_2^-$. The present study suggests that delphinidin is a promising anti oxidative agent.

Electroporation 방법을 이용한 포유동물 세포내 GFP 유전자 도입

  • 양병철;성환후;김동훈;이상기;오현주;임석기;박수봉;이은주;민관식
    • Proceedings of the Korean Society of Embryo Transfer Conference
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    • 2002.11a
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    • pp.70-70
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    • 2002
  • 형질전환 가축을 생산하기 위하여 최근 체세포 복제 기법을 이용하고 있다. 이러한 체세포를 이용한 형질전환 동물의 생산에는 체세포내에 유전자의 도입 효율이 직접적인 영향을 주게 된다. 따라서 본 연구는 세포내 유전자의 transfection 효율을 높이고자 한우의 체세포를 이용하여 여러 가지 조건에서 유전자 도입을 실시하였다. 세포내 유전자 도입 방법은 electroporation (EP) 방법을 이용하였다. 사용한 세포는 소의 귀세포(KbESF), 태아섬유아세포 (KbFF), 그리고 대조구로서 CHO cell을 이용하여 GFP 유전자를 도입하였다. EP는 0.4 cm cuvette을 사용하였고, voltage는 0.25 kV, 그리고 field strength 는 0.625 kV/cm 조건으로 실시하였으며, pulse times은 각각 1, 2, 또는 3회를 사용하였다. KbFF와 KbESF에서는 각각 pulse times을 증가시킬수록 유전자도입 세포수가 증가하였으나 (KbFF: 81, 634, 1,065 cells/$10^{6}$ cells, KbESF: 1,011, 5,567, 15,408 cells/$10^{6}$ cells), CHO cell에서는 pulse times을 증가시킬 수록 오히려 유전자도입 세포수가 감소하였다 (CHO: 1,591, 687, 297 cells/$10^{6}$ cells). 그리고 2주 동안 neo selection을 실시 한 결과 KbFF, KbESF, CHO에서 각각 93, 35, 184 colony가 선발되었으며, 이 중 65.6%, 8.6%, 4.3% 가 GFP 형광 발현 colony로 나타났다. 한편 CHO cell에서 transfection cell수가 감소된 것은 EP의 자극으로 인해 손상된 세포가 많이 발생한 것으로 나타났다. 또한 neo selection에서 선발된 colony중 GFP가 발현되지 않거나 일부만 발현되는 colony들이 많이 발생하였는데, 이것은 세포내 유전자가 transfection되지 않은 세포도 neo selection에서 선발된다는 것을 제시하고 있다. 따라서 체세포를 이용한 형질전환동물 생산을 위해서는 세포내 유전자 도입과 선발 과정에서 나타난 colony에 대하여 보다 엄격한 screen을 하는 것이 필요한 것으로 생각된다.

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Antibody productivity of HBsAg containing both preS2 and S regions expressed in Chinese hamster ovary cells (Chinese hamster ovary세포에서 발현된 pres2 및 S부위 함유 HBsAg의 항체유발능)

  • 정성균;박정민;이상봉;박동우;김동연;김기호;김홍진
    • YAKHAK HOEJI
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    • v.45 no.6
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    • pp.708-714
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    • 2001
  • Many studies have provided evidences that hepatitis B surface antigen (HBsAg) including preS region could be an ideal candidate for a new hepatitis B virus (HBV) vaccine with higher efficacy. We established CHO cell lines, IY-CHO-2 and IY-CHO-11 expressing high levels of HBsAg containing preS2 and S protein by stable transfection method. These cell lines expressed the correct size (about 1 kb in length) of HBsAg mRNA as expected. The purified protein from the culture supernatants of the clones showed the same sizes as those expressed in native hepatitis B virus (24 kDa, 27 kDa, 34 kDa and 36 kDa). Antibody productivity of CHO-derived HBsAg protein at lower dose challenge was higher than the protein containing S region alone expressed in yeast system. These results indicate that CHO-derived HBsAg protein containing preS2 and S region can be effectively used for a better immune response as a HBV vaccine.

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Impact of Anti-Reflective Coating on Silicon Solar Cell and Glass Substrate : A Brief Review

  • Zahid, Muhammad Aleem;Khokhar, Muhammad Quddamah;Cho, Eun-Chel;Cho, Young Hyun;Yi, Junsin
    • Current Photovoltaic Research
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    • v.8 no.1
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    • pp.1-5
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    • 2020
  • The most important factor in enhancing the performance of an optical device is to minimize reflection and increasing transmittance of light for a broad wavelength range. The choice of appropriate coating material is crucial in decreasing reflection losses at the substrate. The purpose of this review is to highlight anti-reflection coating (ARC) materials that can be applied to silicon solar cell and glass substrate for minimizing reflection losses. The optical and electrical behavior of ARC on a substrate is highly dependent on thickness and refractive index (RI) of ARC films that are being deposited on it. The coating techniques and performance of single and multi-layered ARC films after coated on a substrate in a wide range of wavelength spectrum will be studied in the paper.

High Efficiency Crystalline Silicon Solar Cells (고효율 단결정 실리콘 태양전지)

  • Kim, D.S.;Cho, E.C.;Cho, Y.H.;Ebong, A.U.;Min, Y.S.;Lee, S.H.
    • Solar Energy
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    • v.17 no.1
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    • pp.17-26
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    • 1997
  • Since PESC(passivated emitter solar cell) was developed in 1985, high efficiency silicon solar cell technology based on planar technology has been improved in the order of PERC, Point Contact Solar Cell, PERL. BCSC and DSBC, which do not require photolithography, are expected to replace commercial screen printed cells because of its potential for low cost and high efficiency. In this paper, history and characteristics of each type of cells are reviewed.

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Effects of Radioprotectors on DNA Repair Capacity of Tumor Cells

  • Kim, Choon-Mi;Kim, Mi-Kyung
    • Archives of Pharmacal Research
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    • v.16 no.4
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    • pp.259-264
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    • 1993
  • Three cell lines, CHO, L929 and B16 which are non-tumorigenic and cancer cells, respectively, were first tested for their survival in the presence of radioprotective ginseng protein fraction(GPF0. The influence of three radioprotectors-CPF, cysteamine, and 1-Methyl-2-bis[(2-methylthio)vinyl] quinolinium iodide (MVQI) on DNA repair capacity of UV damaged cells survival test, the GPF showed higher cytotoxicity in L929 and B16 than in CHO cells. However, the degree of cell killing was also investigated by measuring $^3H$-thymidine incorporation of PUVA treated cells. In cell survival test, the GPF showed higher cytotoxicity in L929 and B16 than in CHO cells. However, the degree of cell killing was not high enough to consider it as an antitumorigenic agent. Variable results were obtained in the effects on DNA repair capacity depending on the protectors and cell lines used. In pretreatment, the presence of GPF and MVOI brought about a sinificant increase in the capacity in both CHO and B16 cells. However, in L929, the enhancing effect was not shown. In all three cell lines, cysteamine showed lower repair capacity than control, suggesting the primary damage reduction in stronger enhancing effects in L929 and B16 cells, while it was weaker in CHO cells. Here also cystemine hsowed a very little or no increase in the capacity in all three cell lines. These results demonstrate that GPF has mild cytotoxicity in tumorignic cells and that GPF and MVQI enhance DNA repair capacity of UV damaged cells, whether they are tumorigenic or not. On the other hand, cysteamine shows only damage reduction effect. Celles of different genetic origin seem to give different responses to the modifier and different modifiers may possibly work by different mechanisms.

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High Productivity of t-PA in CHO Cells Using Hypoxia Response Element

  • Bae Gun-Won;Jeong Dae-Won;Kim Hong-Jin;Lee Gyun-Min;Park Hong-Woo;Choe Tae-Boo;Kang Seong-Man;Kim Ick-Young;Kim Ik-Hwan
    • Journal of Microbiology and Biotechnology
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    • v.16 no.5
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    • pp.695-703
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    • 2006
  • The dissolved oxygen level of any cell culture environment has a critical effect on cellular metabolism. Specifically, hypoxia condition decreases cell viability and recombinant protein productivity. In this work, to develop CHO cells producing recombinant protein with high productivity, mammalian expression vectors containing a human tissue-type plasminogen activator (t-PA) gene with hypoxia response element (HRE) were constructed and stably transfected into CHO cells. CHO/2HRE-t-PA cells produced 2-folds higher recombinant t-PA production than CHO/t-PA cells in a $Ba^{2+}-alginate$ immobilized culture, and 16.8-folds in a repeated batch culture. In a non-aerated batch culture of suspension-adapted cells, t-PA productivity of CHO/2HRE/t-PA cells was 4.2-folds higher than that of CHO/t-PA cells. Our results indicate that HRE is a useful tool for the enhancement of protein productivity in mammalian cell cultures.