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Vanadium 화합물이 조골세포주 MC3T3-El에 미치는 영향에 관한 연구 (THE EFFECTS OF VANADIUM OXIDE & SODIUM ORTHOVANADATE ON MURIN OSTEOBLAST-LIKE (MC3T3-E1) CELLS)

  • 권기열;정규림
    • 대한치과교정학회지
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    • 제24권1호
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    • pp.17-35
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    • 1994
  • Vanadium is an essential trace element but has not been identified with a specific biogical role. To study the direct effects of vanadium on osteoblast, we incubated murin osteoblast-like (MC3T3-El) cells with various corcentration of vanadium oxide & sodium orthovanadate. This study was designed to investigate the effect of vanadium on DNA synthesis, alkaline phosphatase (ALP) activity, cAMP formation responsive to parathormone(PTH) and type I $\alpha$ 2 collagen ribonucleic acid (mRNA) level in murin osteoblast-like (MC3T3-El) cells. The cells were cultured in $\alpha-minimal$ essential medium$(\alpha-MEM)$ supplemented with $10\%$ fetal bovine serum (FBS) and then changed to $0.1\%$ FBS with various concenoation of vanadium oxide & sodium orthovanadate. Quiescent cultured MC3T3-El cells incubated for 24 hours with 2,5,10,15,20 ${\mu}M$ vanadium oxide incorporated $[^3H]Thymidine;$ every concentration showed increases in $[^3H]Thymidine$ incorporations dose dependant manner, the greatest response occurred at $20{\mu}M$. Quiescent cultured MC3T3-E1 cells incubated for 3days with 2,5,10,15,20 ${\mu}M$ vanadium oxide, for 2days with sodium orthovanadate and alkaline phosphatase was assayed with disodium phenyl phosphate as substrate. Vanadium oxide increased the alkaline phosphatase content in MC3T3-El cells at $2{\mu}M\;&\;6{\mu}M$ ; the greatest response occurred at $2{\mu}M$. But decreased at other content sodium orthovanadate increased alkaline phosphatase content in MC3T3-El cells at all concenoation ; the greatest response occurred at $4{\mu}M$. Quiescent cultured MC3T3-El cells incubated for 3days with $5,10{\mu}M$ vanadium oxide , with $5,8{\mu}M$ sodium orthovanadate and cAMP formation was measured by Radioimmunoassay(RIA). Vanadium oxide & sodium orthovanadate showed the tendency of inhibitory effects on cAMP responsiveness to PTH in MC3T3-El cells. Quiescent cultured MC3T3-El cells incubated for 24hours with $10,20{\mu}M$ vanadium oxide, with $5,10{\mu}M$ sodium orthovanadate and Type I $\alpha$ 2 collagen ribonucleic acid (mRNA) expression was studied by Nothern blot analysis. Northern blot analysis of vanadium oxide treated cells showed decreasing effects 0& sodium orthovanadate revealed increasing effects in type I $\alpha$ 2 collagen ribonucleic acid (mRNA) level.

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회로 최소화를 위한 개선된 Quine-McCluskey 알고리즘 (An Improved Quine-McCluskey Algorithm for Circuit Minimization)

  • 이상운
    • 한국컴퓨터정보학회논문지
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    • 제19권3호
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    • pp.109-117
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    • 2014
  • 본 논문은 회로 최소화 문제에 대한 Quine-McCluskey 법을 개선한 알고리즘을 제안하였다. Quine-McCluskey 법은 주 내포 항을 반복적인 방법으로 찾고, 회로 최소화 방법으로 시행착오법, 분기한정법 또는 Petrick 법을 적용한다. 반면에 제안된 알고리즘은 사전에 항표를 생성하여 주 내포 항을 간단히 찾는 방법을 제안하였으며, 집합피복을 결정하는 방법을 적용하여 1차와 2차 필수 주 내포 항을 간단히 찾는 방법을 제안하였다. 3-변수와 4-변수 실험 데이터에 적용한 결과 제안된 알고리즘이 Quine-McCluskey 법에 비해 보다 간단하면서도 정확히 해를 구할 수 있었다.

근권 정창 세균 Pseudomonas fluorescens MC07의 항진균 활성과 병 억제 능력 (Antifungal Activity of Root Colonizing Pseudomonas fluorescens MC07 is Responsible for Its Disease Suppression Ability)

  • 김진우;박병근;황인규;박창석
    • 한국식물병리학회지
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    • 제14권6호
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    • pp.606-611
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    • 1998
  • An antagonistic bacterium, Pseudomonas flurorescens MC07 inhibited the mycelial growth of Rhizoctonia solani, Pythium ultimum, Fusarium oxysporum, and Phytophthora capsici in on potato dextrose agan (PDA) and other media. The strain MC07 conlonizes various plant roots and possesses antifungal activity. To determine the role of antifungal activity of the bacterium in disease suppression, a mutant Okm3-4 which lost its activity was isolated after screening 2,500 colonies generated by Omegon-Km insertions. The mutant Okm3-4 showed diminished growth inhibition of R. solani, P. ultimum, F. oxysporum, and Ph. capsici in vitro and had reduced suppressive effects on sesame damping.-off compared to the parental strain. In soils, accumulation of the pathogens by continuous cropping, 90% of sesame plants were killed by natural infection of damping-off whereas, only 29% of plants grown from seeds treated with MC07 were killed. On the other hand, 85% of plants died when sesame seeds were treated with the Okm3-4 cells. This indicated that antifungal activity of MC07 in vitro is directly responsible for the suppression of damping-off disease. Emergence rates of sesame seeds in pots containing diseased soil were 33%. However, MC07 treatments on seeds significantly improved emergence rates, which has similar effects of Benomyl treatment. The mutant Okm3-4 exhibited 53% of emergence rate. This indicated that antifungal activity of MC07 also affects the emergence rate of sesame seeds.

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유향 추출물이 MC3T3-E1 세포 활성 및 분화에 미치는 영향 (Effects of Olibanum Extracts on the Activity and Differentiation of MC3T3-E1 Cells)

  • 한상헌;김명동;유승한;유용욱;유형근;신형식
    • Journal of Periodontal and Implant Science
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    • 제31권2호
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    • pp.287-298
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    • 2001
  • Recently, many natural medicines, which have advantage of less side effects and possibility of long-term use have been studied for their capacity of anti-bacterial, anti-inflammatory and regenerative potential of periodontal tissues. Olibanum has the effects to hemostasis, analgesic and anti-inflammatory, and it also has been traditionally used as a drug for the treatment of bone disease in oriental medicine. The purpose of the present study was to investigate the effects of Olibanum extracts on the activity and differentiation of MC3T3-E1 cells, alkaline phosphatase(ALP) synthesis, formation of bone nodules and expression of type I collagen of MC3T3-E1 cells. To examine the cellular activity, MC3T3-E1 cells were cultured with ${\alpha}-MEM(control)$ and each concentration of Olibanum for 2 days and 4 days. To compare the ALP synthesis, MC3T3-E1 cells were cultured with ${\alpha}-MEM(negative\; control)$, dexamethasone(positive control), and each concentration of Olibanum for 2 days and 4 days. To compare the bone nodule formation, MC3T3-E1 ells were cultured for 21 days, and to compare the type I collagen expression, MC3T3-E1 cells were cultured for 4 days. The cellular activity of MC3T3-E1 cells treated with $1{\mu}g/ml$ of Olibanum extracts was significantly increased at 4-day(p<0.05) to control. The activity of ALP in MC3T3-E1 cells treated with $1{\mu}g/ml$ Olibanum extracts was significantly increased at 4-day(p<0.05). All the experimental groups showed much more bone nodule formation than control groups. The group treated with $1{\mu}g/ml$ of Olibanum extracts was the highest bone nodule formation, and showed much more type I collagen expression than negative control. These results indicate that Olibanum extracts may be considered effective in the activity and differentiation of MC3T3-E1 cells.

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칡소의 MC1R의 유전자형에 따른 교배 조합이 자손의 모색과 유전자형 변이에 미치는 영향 (Effects of Genotype Mutation and Coat Color Phenotype on the Offspring from Mating System of MC1R Genotype Patterns in Korean Brindle Cattle)

  • 김상환;정경섭;이호준;백준석;정덕원;김대은;윤종택
    • 한국수정란이식학회지
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    • 제28권3호
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    • pp.215-222
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    • 2013
  • Bovine coat color is decided by the melanocortin receptor 1 (MC1R) genotype mutation and melanogenesis. Specially, in the various cattle breeds, dominant black coat color is expressed by dominant genotype of $E^D$, red or brown is expressed in the frame shift mutation of recessive homozygous e by base pair deletion and wild type of $E^+$ is expressed in various coat colors. However, not very well known about the effected of MC1R genotype mutation on the coat color through family lines in KBC. Therefore, this study were to investigate effect of MC1R genotype mutation on the coat color, and to suggest mating breed system in accordance with of MC1R genotype for increased on brindle coat color appearance. Parents (sire 2 heads and dam 3 heads) and offspring (total : 54 heads) from crossbreeding in KBC family line with the MC1R genotype and phenotype records were selected as experimental animals. The relationship between melanocortin 1 receptor (MC1R) genotypes expression verified by PCR-RFLP, and brindle coat color appearance to the family line of the cross mating breed from MC1R genotype pattern was determined. As a result, 4MC1R genetic variations, $E^+/E^+$ (sire 1), $E^+/e$ (sire 2 and dam 3), $E^+/e$ with 4 bands of 174, 207 and 328 bp (dam 1) and $E^+/e$ with 3 bands of 174, 207, 328 and 535 bp (dam 2) from parents (sire and dam) of KBC. However, 3 genetic variations, e/e (24%), $E^+/E^+$ (22%) and $E^+/e$ (56%) were identified in offspring. Also, brindle coat color expressrated was the e/e with the 0%, $E^+/E^+$ with 67% and $E^+/e$ with 77% from MC1R genotype in offspring on the cross mating of KBC. Furthermore, when the sire had $E^+/e$ genotype and the dam had $E^+/E^+$ with the 3 bands or $E^+/e$ genotype, and both had whole body-brindle coat color, 62% of the offspring had whole body-brindle coat color. Therefore, the seresults, the mating system from MC1R genotype patterns of the sires ($E^+/e$) and dams ($E^+/E^+$ with the 3 bands or $E^+/e$) with brindle coat color may have the highest whole body-brindle coat color expression in their offspring.

Development of Melanotropin Antagonists: Investigating Potent and Specific Ligands for New Receptors

  • Lim, Sejin
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1996년도 제4회 추계심포지움
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    • pp.153-159
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    • 1996
  • ${\alpha}$-Melanotropin (Ac-Ser-Tyr- Ser-Met-Glu$\^$5/-His-Phe-Arg-Trp-Gly$\^$10/-Lys-Pro-Val-NH$_2$) is one of the first peptide hormones to be isolated and have its structure determined. It was early recognized to have essentially the same N-terminal tridecapeptide sequence as adrenocorticotropic hormone (ACTH) except that the N-terminal was acetylated in the case of ${\alpha}$-MSH but not in the case of ACTH, indicating that their biosyntheses were different (Figure 1). Subsequently it was discovered that ${\alpha}$-MSH and ACTH were derived from the same gene, currently referred to as proopiomelanocortin (POMC). Its original bioactivity was pigmentation, but it also was recognized that it may have activity in the central nervous system, though the precise nature of these central activities have been controversial. The recent cloning and expression of five melanocortin receptors, with the MC3 and MC4 receptors found primarily in the brain and the MC5 receptor (MC5-R) found throughout the body, has provided new impetus to understand the structure-activity relationships of ${\alpha}$-MSH at these receptors. The effects of ${\alpha}$-MSH on pigmentation are mediated by the MC1-R expressed specifically on the surface of melanocytes. Similarly the MC2-R is involved in the regulation of adrenal steroidogenesis by ACTH. However, given the complexity of expression of the MC3, MC4, and MC5 receptors, it has not been possible to identify any simple correlations between these receptors and the reported biological activities of the melanocortin peptides. Consequently, potent and receptor specific agonists and especially antagonists would be extremely valuable tools for the determination of the physiological roles of the MC3, MC4, and MC5 receptors. Though the extensive structure-activity relationships have provided much information on agonist activity related to pigmentary effects, only recently has it been possible to begin to systematically develop potent and selective antagonists.

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산양삼의 조골세포 활성화에 미치는 영향 (Effects of Wild Simulated Ginseng on the Proliferation, Differentiation and Mineralization of Osteoblastic MC3T3-E1 Cells)

  • 정진부
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2020년도 춘계학술대회
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    • pp.90-90
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    • 2020
  • Panax ginseng C.A. Meyer (P. ginseng) is known to exert a wide range of pharmacological effects both in vitro and in vivo. Although studies on ginsenoside, antioxidant activity, and anticancer effect of wild simulated ginseng (WSG) have been conducted, there is little research on the effect of WSG on bone metabolism. In this study, we investigated the potential anti-osteoporotic properties of WSG on the growth and differentiation of MC3T3-E1 cells. WSG significantly increased the viability and proliferation of MC3T3-E1 cells. WSG activated intracellular alkaline phosphatase (ALP) activity in MC3T3-E1 cells. In addition, WSG increased the mineralized nodules in MC3T3-E1 cells. Furthermore, WSG increased the expression of genes such as Runx2, ALP, OPN and OCN associated with osteoblast growth and differentiation in a dose-dependent manner.

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MC-CDMA 방식을 적용한 UWB 시스템의 성능평가 (Performance of MC-CDMA Based UWB System)

  • 김철순;곽경섭;이형기
    • 한국멀티미디어학회논문지
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    • 제9권1호
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    • pp.51-58
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    • 2006
  • 본 논문은 최근 표준화(IEEE802.15.3a)가 진행중인 Ultra Wideband(UWB) 시스템에서 현재 제안된 방식인 DS-CDMA 방식과 OFDM 방식을 혼합한 형태인 MC-CDMA 방식을 UWB 시스템에 적용하고, 그 성능을 평가한다. DS-CDMA 방식은 다중경로 성분을 검출하기 위해 많은 Rak Finger들이 필요하기 때문에 시스템의 복잡도가 증가하고 OFDM 방식은 주파수 호평을 끈 상태에서 방사 전력이 FCC에서 규정을 만족하지 못한다. 따라서 두 시스템의 혼합 형태인 MC-CDMA 방식이 시스템의 복잡도는 D5-CDMA 보다 간단하면서 주파수 선택적 페이딩 채널에서 좋은 성능을 발휘하고 OFDM 방식보다 넓은 대역폭을 사용함으로써 스펙트럼당 방사 전력이 낮아진다. MC-CDMA 방식을 수식적으로 분석하고 DS-CDMA, OFDM 방식과 시뮬레이션을 통해 성능을 비교하였다.

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다중경로 레일리 페이딩 채널에서 Turbo 부호를 적용한 MC DS-CDMA 시스템의 성능 분석 (Performance Analysis of MC DS-CDMA System using Turbo Code in Multipath Rayleigh Fading Channel)

  • 박기식
    • 한국정보통신학회논문지
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    • 제5권5호
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    • pp.902-907
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    • 2001
  • 본 논문에서는 다중 경로 레일리 페이딩 채널에서 MC DS-CDMA 시스템의 BER 성능을 분석하였고, 최근에 가장 강력한 부호화 기법으로 급부상하고 있는 터보 코드를 MC DS-CDMA 시스템에 적용하여 성능 개선 정도를 평가하였다. 성능 해석 결과, 레일리 페이딩 채널에서는 강력한 성능 개선 기법을 적용하지 않는 한 사용자 수와 E/sub b//N/sub o/ 값에 관계없이 음성 서비스 (BER : 10/sup -3/)를 지원하지 못함을 알 수 있었다. 한편, 터보 코드를 성능 개선 기법으로 적용하면 BER 성능이 매우 개선되고, 사용자 수와 E/sub b//N/sub o/ 값에 관계없이 음성 서비스를 충분히 지원할 수 있음을 알 수 있었다 예를 들어 E/sub b//N/sub o/가 10 ㏈이고 사용자 수가 10 명인 경우, 터보 코드를 적용함에 의해 BER 성능이 약 5x10/sup -3/ 정도 개선됨을 알 수 있었다.

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Chemical Constituents from Acer mandshuricum and Their Effects on the Function of Osteoblastic MC3T3-E1 Cells

  • Ding, Yan;Liang, Chun;Nguyen, Huu Tung;Choi, Eun-Mi;Kim, Jeong-Ah;Kim, Young-Ho
    • Bulletin of the Korean Chemical Society
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    • 제31권4호
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    • pp.929-933
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    • 2010
  • A new compound, 4-methoxyl 5-hydroxymethyl benzoic 3-O-$\beta$-D-glucopyranoside (1), has been isolated from the leaves and stems of Acer mandshuricum, along with nine known compounds (2-10). Their structures were determined by a variety of spectroscopic analyses. The effect of compounds 1-10 on the function of osteoblastic MC3T3-E1 cells was examined by determining alkaline phosphatase (ALP) activity, collagen synthesis, and mineralization. Compound 1 significantly increased the function of osteoblastic MC3T3-E1 cells; $5.0\;{\mu}M$ of 1 increased ALP activity, collagen synthesis, and mineralization of MC3T3-E1 cells to 114.7, 119.5, and 108.2% (P < 0.05) of the basal value, respectively. In addition, compounds 2-10 also potently increased the function of osteoblastic MC3T3-E1 cells.