• 제목/요약/키워드: lethal target

검색결과 57건 처리시간 0.033초

Development of an In Vitro Test System Measuring Transcriptional Downregulatory Activities on IL-13

  • Choi, Jeong-June;Park, Bo-Kyung;Park, Sun-Young;Yun, Chi-Young;Kim, Dong-Hee;Kim, Jin-Sook;Hwang, Eun-Sook;Jin, Mi-Rim
    • Journal of Microbiology and Biotechnology
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    • 제19권3호
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    • pp.331-337
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    • 2009
  • Interleukin-13 (IL-13) has been proposed as a therapeutic target for bronchial asthma as it plays crucial roles in the pathogenesis of the disease. We developed an in vitro test system measuring transcriptional downregulatory activities on IL-13 as a primary screening method to select drug candidates from natural products. The promoter region of IL-13 (-2,048 to +1) was cloned into the upstream of a luciferase gene in the plasmid pGL4.14 containing the hygromycin resistance gene as a selection marker, generating pGL4.14-IL-13. The EL-4 thymoma and RBL-2H3 mast cells transiently expressing this plasmid highly produced the luciferase activities by responding to PI (PMA and ionomycin) stimulation up to 8-fold and 13-fold compared with the control, respectively, whereas cyclosporin A, a well-known antiasthmatic agent, significantly downregulated the activities. The BF1 clone of RBL-2H3 cells constitutively expressing pGL4.14-IL-13 was established by selecting surviving cells under a constant lethal dose of hygromycin treatment. The feasibility of this system was evaluated by measuring the downregulatory activities of 354 natural products on the IL-13 promoter using the BF1 clone. An extract from Morus bombycis (named TBRC 156) significantly inhibited PI-induced luciferase activities and IL-13 mRNA expression, but not the protein expression. Fisetin (named TBRC 353) inhibited not only PI-induced luciferase activities and mRNA expression, but also the IL-13 protein secretion, whereas myricetin (named TBRC 354) could not suppress the IL-13 expression at all. Our data indicated that this in vitro test system is able to discriminate the effects on IL-13 expression, and furthermore, that it might be suitable as a simple and time-saving primary screening system to select antiasthmatic agents by measuring transcriptional activities of the IL-13 promoter.

Functional Expression of P2Y Receptors in WERI-Rb1 Retinoblastoma Cells

  • Kim, Na-Hyun;Park, Kyu-Sang;Sohn, Joon-Hyung;Yeh, Byung-Il;Ko, Chang-Mann;Kong, In-Deok
    • The Korean Journal of Physiology and Pharmacology
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    • 제15권1호
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    • pp.61-66
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    • 2011
  • P2Y receptors are metabotropic G-protein-coupled receptors, which are involved in many important biologic functions in the central nervous system including retina. Subtypes of P2Y receptors in retinal tissue vary according to the species and the cell types. We examined the molecular and pharmacologic profiles of P2Y purinoceptors in retinoblastoma cell, which has not been identified yet. To achieve this goal, we used $Ca^{2+}$ imaging technique and western blot analysis in WERI-Rb-1 cell, a human retinoblastoma cell line. ATP ($10\;{\mu}M$) elicited strong but transient $[Ca^{2+}]_i$ increase in a concentration dependent manner from more than 80% of the WERI-Rb-1 cells (n=46). Orders of potency of P2Y agonists in evoking $[Ca^{2+}]_i$ transients were 2MeS-ATP>ATP>>UTP=${\alpha}{\beta}$-MeATP, which was compatible with the subclass of $P2Y_1$ receptor. The $[Ca^{2+}]_i$ transients evoked by applications of 2MeS-ATP and/or ATP were also profoundly suppressed in the presence of $P2Y_1$ selective blocker (MRS 2179; $30\;{\mu}M$). $P2Y_1$ receptor expression in WERI-Rb-1 cells was also identified by using western blot. Taken together, $P2Y_1$ receptor is mainly expressed in a retinoblastoma cell, which elicits $Ca^{2+}$ release from internal $Ca^{2+}$ storage sites via the phospholipase C-mediated pathway. $P2Y_1$ receptor activation in retinoblastoma cell could be a useful model to investigate the role of purinergic $[Ca^{2+}]_i$ signaling in neural tissue as well as to find a novel therapeutic target to this lethal cancer.

PED 바이러스 Spike 단백질의 세포 수용체 결합 부위 확인 (The N-terminal Region of the Porcine Epidemic Diarrhea Virus Spike Protein is Important for the Receptor Binding)

  • 이동규;차세연;이창희
    • 한국미생물·생명공학회지
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    • 제39권2호
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    • pp.140-145
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    • 2011
  • 돼지유행성설사 바이러스(porcine epidemic diarrhea virus: PEDV)는 자돈에게 감염 시 수양성설사를 동반한 급성 장염을 유발하며 매우 높은 폐사율을 보이는 그룹 1 코로나바이러스이다. PEDV는 다른 그룹 1 코로나바이러스와 마찬가지로 숙주 세포에 감염 시 aminopeptidase N (APN)을 세포 수용체로 이용한다고 알려져 있다. 코로나바이러스의 spike(S) 단백질은 숙주세포의 표면에 부착과 관련하여 감염 개시에 있어 중요한 역할을 하는 것으로 알려져 있으며 특히 S 단백질의 S1 도메인은 세포 수용체에 특이적인 결합을 매개하는 수용체 결합 도메인(receptor binding domain: RBD)을 포함하고 있는 것으로 알려져 있다. 이미 많은 코로나바이러스의 RBD의 위치가 확인되어져 있지만 PEDV의 RBD에 대해서는 아직까지 알려진 바가 없다. 본 연구에서는 돼지 APN 수용체와 결합을 매개하는 PEDV의 RBD를 규명하기 위해 S1 도메인을 주형으로 하는 일련의 재조합 truncated variant들을 제작하였고 각각의 truncated들이 실제로 pAPN과의 결합을 이루는지에 대하여 실험을 통해 확인하였다. 그 결과 S1 도메인의 N 말단 부분이 pAPN과의 결합에서 중요한 부위임을 확인할 수 있었다. 본 연구에서 도출된 결과는 향후 PEDV의 S 단백질과 pAPN간의 분자적 상호작용을 이해하는 데에 도움을 줄 것으로 판단된다.

Evaluation of General Toxicity and Genotoxicity of the Silkworm Extract Powder

  • Heo, Hyun-Suk;Choi, Jae-Hun;Oh, Jung-Ja;Lee, Woo-Joo;Kim, Seong-Sook;Lee, Do-Hoon;Lee, Hyun-Kul;Song, Si-Whan;Kim, Kap-Ho;Choi, Yang-Kyu;Ryu, Kang-Sun;Kang, Boo-Hyon
    • Toxicological Research
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    • 제29권4호
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    • pp.263-278
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    • 2013
  • The silkworm extract powder contain 1-deoxynojirimycin (DNJ), a potent ${\alpha}$-glycosidase inhibitor, has therapeutic potency against diabetes mellitus. Therefore, natural products containing DNJ from mulberry leaves and silkworm are consumed as health functional food. The present study was performed to evaluate the safety of the silkworm extract powder, a health food which containing the DNJ. The repeated toxicity studies and gentic toxicity studies of the silkworm extract powder were performed to obtain the data for new functional food approval in MFDS. The safety was evaluated by a single-dose oral toxicity study and a 90 day repeated-dose oral toxicity study in Sprague-Dawley rats. The silkworm extract powder was also evaluated for its mutagenic potential in a battery of genetic toxicity test: in vitro bacterial reverse mutation assay, in vitro chromosomal aberration test, and in vivo mouse bone marrow micronucleus assay. The results of the genetic toxicology assays were negative in all of the assays. The approximate lethal dose in single oral dose toxicity study was considered to be higher than 5000 mg/kg in rats. In the 90 day study, the dose levels were wet at 0, 500, 1000, 2000 mg/kg/day, and 10 animals/sex/dose were treated with oral gavage. The parameters that were monitored were clinical signs, body weights, food and water consumptions, ophthalmic examination, urinalysis, hematology, serum biochemistry, necropsy findings, organ weights, and histopathological examination. No adverse effects were observed after the 90 day administration of the silkworm extract powder. The No-Observed-Adverse-Effect-Level (NOAEL) of silkworm extract powder in the 90 day study was 2000 mg/kg/day in both sexes, and no target organ was identified.

머리대장가는납작벌레의 합리적 방제 물질로 이란 서양가새풀 정유의 살충효과 평가 (Essential Oil Isolated from Iranian Yarrow as a Bio-rational Agent to the Management of Saw-toothed Grain Beetle, Oryzaephilus surinamensis (L.))

  • 아스가르 에바돌라히
    • 한국응용곤충학회지
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    • 제56권4호
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    • pp.395-402
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    • 2017
  • 유기합성 농약의 과다사용은 환경오염, 살충제 저항성 발달, 비표적 생물에 대한 영향 등 부작용의 원인이 되고 있다. 유기합성 농약의 대체약제로 포유동물에 저독성인 식물기원 물질이 각광을 받게 되었다. 이란 서양가새풀(Achillea millefolium L.) 정유성분의 훈증독성은 국제적 저장작물 해충인 머리대장가는납작벌레(Oryzaephilus surinamensis L.)의 방제제로 연구된 바 있다. 이 식물 정유의 화학적 성분을 가스크로마트 그래피(MS)를 이용하여 분석하였다. 살충실험 결과 처리농도에 따라 유의한 살충률을 나타냈다. 처리농도와 살충률 간 양의 상관관계가 있었다. 반치사 농도(LC50)는 $17.977{\mu}l/L$ 이었다. 주요 성분은 1,8-Cineole (13.17%), nerolidol (12.87%), ${\alpha}$-cubebene (12.35%), artemisia ketone (6.69%), ${\alpha}$-terpineol (5.27%), alloaromadendrene oxide (4.71%) 및 borneol (3.99%) 이었다. 전체 동정된 화합물의 96.35%는 Terpenic 화합물로 monoterpene hydrocarbons (8.19%), monoterpenoids (44.23%), sesquiterpene hydrocarbons (21.69%) 및 sesquiterpenoids (22.24%)를 포함하고 있었다. 본 결과는 terpene이 풍부한 서양가새풀 정유가 머리대장가는납작벌레의 안전한 생물농약으로 고려될 수 있음을 보여주었다.

실행방식 측면에서 살충제의 신중한 사용에 의한 저항성 발달의 관리 (Management of the Development of Insecticide Resistance by Sensible Use of Insecticide, Operational Methods)

  • 정부근;박정규
    • 한국응용곤충학회지
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    • 제48권2호
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    • pp.123-158
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    • 2009
  • 해충의 저항성발달로 야기되는 문제를 해결하기 위한 정보를 제공함으로써 향후연구를 촉진시키고자 하였다. 농약사용이 지속되는 한 저항성 발달은 필연적이라는 생각으로, 저항성발달을 지연시키기 위해 재배자가 활용할 수 있는 약제성질에 근거를 둔 약종선택, 혼용, 교호, 모자이크 처리 등 약제살포법과, 천적과 양립할 수 있는 선택성 살충제와 저항성 천적의 이용을 중심으로 한 병해충 종합관리(IPM)에 대해 고찰하였다. 저항성관리에 약종의 성질을 이용할 경우 약종별로 작용점과 mode of action(작용방식)이 같거나 다를 수 있고, 2차 해충과 함께 살충제의 활성, 잔류기간, 약제 저항성 발달에 대한 취약성도 다르다. 약제는 섭식, locomotion(거동), 비행, 교미, 포식자 회피 등에도 영향을 미치므로 종합적으로 고려하여 역교차저항성을 나타내는 살충제의 사용이 바람직하다. 농약혼용은 실제 많이 이루어지고 있고 앞으로도 그러하겠지만, 진정한 의미에서 저항성 발달 지연을 위한 혼용, 교호, 모자이크 처리법은 대립유전자의 우성도, 교차저항성, 유입(immigration), fitness 불이익 등과 함께 살충제의 작용방식과 작용점들의 차이에서 구성약제가 매우 높은 비율로 충을 죽이는 부의 교차저항성을 가진 살충제들의 채택에 대하여 논의하였다. 저항성 관리에 약제혼용의 대표적인 사례 22가지와 교호처리 사례 27가지를 표로 제시하였다. 혼용처리의 잠재적 불이익은 생물적 방제의 와해, 이차해충의 저항성발달, 고도의 저항성 개체군 선발, 다양한 살충제에 대한 교차저항성 범위 확대를 내포하고 있다. 교호처리는 살포약량을 높이거나 낮추고, 다른 대사기구를 가진 살충제를 사용하는 것도 고려되었다. 모자이크 처리는 진딧물 같이 정주성 해충인 경우에 연관없는 살충제를 교호로 다른 구역에 처리하거나, 살충제 처리한 열(列)과 그렇지 않은 것을 혼합 배치하여 저항성 발달을 지연시키거나 피해를 감소시킬 수 있다. 해충의 저항성 진화 측면에서 볼 때, 기생자와 포식자의 저항성과 선택성은 농약처리를 요하는 세대 수를 감소시키고 농약으로부터 피난처의 상보적 역할을 수행할 수 있다. 작물별, 기주별, 기생자와 포식자에게 선택성을 보이는 약제를 별도의 표로 요약하여 제시하였다. 기생자의 생존력 향상을 위해 살충제의 선택성과 선택성에 영향을 주는 내 외적 요인에 대하여 검토하였다. 농약사용 하에서 기생자를 사용하기 위해 농약에 대해 저항성이거나 내성이 있는 기생자를 검정, 채집 혹은 선발하는 것을 논의하였다. 포식자에 대한 선택독성에 영향을 미치는 요인들로 농약의 선택성, 선택성의 포장적용과 그에 미치는 요인, 포식자와 기주의 균형, 선택성을 도외시한 방제법의 문제점, 천적과 농약의 양립성 등에 대하여 논의하였다.

X-선(線) 조사(照射)가 Ehrlich 암세포(癌細胞)의 용적(容積), 단백양(蛋白量) 및 수종(數種) Sulfhydryl 기(基)에 미치는 영향(影響)에 관(關)하여 (Effect of X-Irradiation on the Levels of some Sulfhydryl Groups, Protein and Cell Volume of Ehrlich Ascites Tumour Cells)

  • 유춘식;주영은
    • The Korean Journal of Physiology
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    • 제3권2호
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    • pp.9-16
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    • 1969
  • It is well known that a number of -SH and -SS containing substances afford a certain measure of protection against radiation effects in many biological systems, and it is conceivable that inherent -SH levels in Ehrlich ascites tumour (ELD)cells may be of decisive improtance with respect to the development of cellular radiation injury. So far, little effort has been directed to elucidate the changes in levels of different -SH and -SS groups in ELD cells when the tumour-bearing whole animal was subjected to the sublethal dose of X-irradiation. The present study was designed to bring some lights in the possible changes of and relationship between various sulfhydryl levels, such as P-SH, NP-SH and NP-SS, as well as the content of protein and cell volume of ELD cells, after subjecting the ELD mice to 1,200 r of X-irradiation. The animals used in this experiment were all mixed bred mice of $20{\sim}25\;gm$ in body weight (approximately 2 months old) irrespective of sex. 12 mice in one experiment were inoculated intraperitoneally with 0.2 ml of ascites tumour cells $(2{\times}10^6\;cells)$, and on the 7th day of the tumour growth, they were X-irradiated with 1,200 r, using the conventional X-ray machine under the following conditions: 200 Kv at 15 mA, 0.5 mm Cu filter, target-skin distance: 50 cm. Radiation dose was measured with the the Philip integrating dosimeter. At 24, 36, 48 and 60 hours after the X-irradiation, the mice were killed by cervical dislocation, and the tumours were taken out. Freshly withdrawn ascites tumours were placed in ice, and immediately the cell concentration was measured with the Coulter Cell Counter (Model B), and the hematocrit of the tumour cells were also determined. Cell volume was thus calculated by the cell concentration and hematocrit value. P-SH content of ELD cells was measured potentiometrically according to the method of Calcutt & Doxey, and NP-SH and NP-SS contents were measured spectrophotometrically by the method described by Ellman. Protein content of ELD cells was determined with the Folin phenol reagent by Lowry et al. Altogether, 48 experimental mice were used, and 12 mice with the only exception of X-irradiation were used as the control. Results obtained indicate that the contents of all the cellular sulfhydryl groups as well as cell volume and protein content of the ELD cells increase significantly as time progresses after the sub-lethal X-ray dose of 1,200 r was given and that all the increase is in a lineal fashion. The regression lines of the relative values, (i. e., taking each control value as 1) of all the values obtained, and the regression lines of cell volume, protein and NP-SH are identical, whereas those of NP-SS and P-SH appear to be widely seperated. However, the difference of those two lines (NP-SS & P-SH) were found to be not significant statistically (p>0.05). Therefore, it can be concluded from the above results that all the values examined increase in a lineal fashion with no statistically significant difference among them. Also, with the radiation dose of 1,200 r, the ELD cell becomes enlarged and swollen progressively up to 60 hours post-irradiation and it becomes more than two times of the original normal size at 60 hours after the irradiation, and up to this stage, it seems apparent that the cell division has been slow due to the X-irradiation applied in this experiment. It is well understandable that the contents of NP-SH, NP-SS, P-SH and protein of the ELD cells increase in parallel with the increase of the cell volume by the X-ray does used, but it also seems interesting to note that all the cellular substances tested show no appreciable difference in the pattern of increase.

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