• 제목/요약/키워드: MIB-1

검색결과 988건 처리시간 0.026초

이종의 영상부호화 표준간의 변환부호화에서 화면내 부호화를 위한 효율적인 재양자화 기법 (An Efficient Requantization Method for INTRA Frames in Heterogeneous Transcoding)

  • 서광덕;김재균
    • 전기전자학회논문지
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    • 제5권2호
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    • pp.221-231
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    • 2001
  • 본 논문에서는 MPEG-1을 MPEG-4 심플 프로파일로 변환 부호화할 때 화면내 부호화를 위한 효율적인 재양자화 기법에 대해 제안한다. MPEG-1의 화면내 부호화 블록의 양자화는 양자화 가중 행렬을 사용하는 반면, MPEG-4 심플 프로파일은 양자화 가중 행렬을 사용하지 않는다. 그 결과 두 부호화 방식의 양자화에 사용되는 양자화 파라미터가 동일하더라도 양자화 계단 크기가 서로 달라지기 때문에 변환 부호화된 MPEG-4 영상의 화질이 심하게 열화 된다. 이 문제를 해결하기 위해 변환 부호기에서 양자화 오차를 최소화하는 재생레벨을 결정하는 방식을 제안하며, 이 방식의 적용을 위해 변환부호기에서 MPEG-1 시퀸스의 DCT 계수에 대한 확률밀도함수를 추정하는 방법을 제시한다. 실험결과에 의하면 제안된 방식을 적용할 경우 기존의 방식에 비해 PSNR 측면에서 $0.3{\sim}0.6dB$ 정도의 개선이 있으며, 동시에 발생 비트량을 $5{\sim}7%$ 정도 줄일 수 있다.

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유방암세포 성장과 Bmi-1 발현에 대한 레스베라트롤의 억제 효과 (Resveratrol Down-regulates Bmi-1 Expression and Inhibits Breast Cancer Cell Growth In Vitro)

  • 박현주;박광제;옥창엽;장혜옥;배문경;배수경
    • KSBB Journal
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    • 제32권3호
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    • pp.224-232
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    • 2017
  • Resveratrol has been actively investigated as an anticancer drug since it induces cell growth inhibition and apoptosis in many cancer cells. Resveratrol acts through modulation of multiple pathways and genes. In this study, we found resveratrol reduced cell growth and mammosphere formation in MDA-MB-231 triple-negative human breast cancer cells. This suppressive effect of resveratrol is accompanied by a reduction in Bmi-1 gene expression. We also observed that knock-down of Bmi-1 gene by small interfering RNA effectively sensitizes breast cancer cells to resveratrol treatment. Our data demonstrate, for the first time, that resveratrol down-regulates Bmi-1 expression in human breast cancer cells and suggest that specific molecular targeting of Bmi-1 can be combined with a chemotherapeutic strategy to improve the response of breast cancer cells to resveratrol.

Identification of genomic diversity and selection signatures in Luxi cattle using whole-genome sequencing data

  • Mingyue Hu;Lulu Shi;Wenfeng Yi;Feng Li;Shouqing Yan
    • Animal Bioscience
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    • 제37권3호
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    • pp.461-470
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    • 2024
  • Objective: The objective of this study was to investigate the genetic diversity, population structure and whole-genome selection signatures of Luxi cattle to reveal its genomic characteristics in terms of meat and carcass traits, skeletal muscle development, body size, and other traits. Methods: To further analyze the genomic characteristics of Luxi cattle, this study sequenced the whole-genome of 16 individuals from the core conservation farm in Shandong region, and collected 174 published genomes of cattle for conjoint analysis. Furthermore, three different statistics (pi, Fst, and XP-EHH) were used to detect potential positive selection signatures related to selection in Luxi cattle. Moreover, gene ontology and Kyoto encyclopedia of genes and genomes pathway enrichment analyses were performed to reveal the potential biological function of candidate genes harbored in selected regions. Results: The results showed that Luxi cattle had high genomic diversity and low inbreeding levels. Using three complementary methods (pi, Fst, and XP-EHH) to detect the signatures of selection in the Luxi cattle genome, there were 2,941, 2,221 and 1,304 potentially selected genes identified, respectively. Furthermore, there were 45 genes annotated in common overlapping genomic regions covered 0.723 Mb, including PLAG1 zinc finger (PLAG1), dedicator of cytokinesis 3 (DOCK3), ephrin A2 (EFNA2), DAZ associated protein 1 (DAZAP1), Ral GTPase activating protein catalytic subunit alpha 1 (RALGAPA1), mediator complex subunit 13 (MED13), and decaprenyl diphosphate synthase subunit 2 (PDSS2), most of which were enriched in pathways related to muscle growth and differentiation and immunity. Conclusion: In this study, we provided a series of genes associated with important economic traits were found in positive selection regions, and a scientific basis for the scientific conservation and genetic improvement of Luxi cattle.

Genetic disruption of ATAT1 causes RhoA downregulation through abnormal truncation of C/EBPβ

  • Jee-Hye Choi;Jangho Jeong;Jaegu Kim;Eunae You;Seula Keum;Seongeun Song;Ye Eun Hwang;Minjoo Ji;Kwon-Sik Park;Sangmyung Rhee
    • BMB Reports
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    • 제57권6호
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    • pp.293-298
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    • 2024
  • Microtubule acetylation has been shown to regulate actin filament dynamics by modulating signaling pathways that control actin organization, although the precise mechanisms remain unknown. In this study, we found that the downregulation of microtubule acetylation via the disruption ATAT1 (which encodes α-tubulin N-acetyltransferase 1) inhibited the expression of RhoA, a small GTPase involved in regulating the organization of actin filaments and the formation of stress fibers. Analysis of RHOA promoter and chromatin immunoprecipitation assays revealed that C/EBPβ is a major regulator of RHOA expression. Interestingly, the majority of C/EBPβ in ATAT1 knockout (KO) cells was found in the nucleus as a 27-kDa fragment (referred to as C/EBPβp27) lacking the N-terminus of C/EBPβ. Overexpression of a gene encoding a C/EBPβp27-mimicking protein via an N-terminal deletion in C/EBPβ led to competitive binding with wild-type C/EBPβ at the C/EBPβ binding site in the RHOA promoter, resulting in a significant decrease of RHOA expression. We also found that cathepsin L (CTSL), which is overexpressed in ATAT1 KO cells, is responsible for C/EBPβp27 formation in the nucleus. Treatment with a CTSL inhibitor led to the restoration of RHOA expression by downregulation of C/EBPβp27 and the invasive ability of ATAT1 KO MDA-MB-231 breast cancer cells. Collectively, our findings suggest that the downregulation of microtubule acetylation associated with ATAT1 deficiency suppresses RHOA expression by forming C/EBPβp27 in the nucleus through CTSL. We propose that CTSL and C/EBPβp27 may represent a novel therapeutic target for breast cancer treatment.

Construction of Deletion Map of 16q by LOH Analysis from HCC Patients and Physical Map on 16q 23.3 - 24.1 Region

  • Chung, Jiyeol;Choi, Nae Yun;Shim, Myoung Sup;Choi, Dong Wook;Kang, Hyen Sam;Kim, Chang Min;Kim, Ung Jin;Park, Sun Hwa;Kim, Hyeon;Lee, Byeong Jae
    • Genomics & Informatics
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    • 제1권2호
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    • pp.101-107
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    • 2003
  • Loss of heterozygosity (LOH) has been used to detect deleted regions of a specific chromosome in cancer cells. LOH on chromosome 16q has been reported to occur frequently in progressed hepatocellular carcinoma (HCC). Liver tissues from 37 Korean HCC patients were analyzed for LOH by using 25 polymorphic microsatellite markers distributed along 16q. Out of the 37 HCC patients studied, 21 patients (56.8%) showed LOH in various regions of 16q with at least one polymorphic marker. Puring the analysis of these 21 LOH cases, 6 patients showed interstitial LOHs in which the boundary of the LOH region was defined. With two rounds of LOH analysis, five commonly occurring interstitial LOH regions were identified; 16q21-22.1, 16q22.2 - 22.3, 16q22.3, 16q23.2 and 16q23.3 - 24.1. Among the five LOH regions the 16q23.3 - 24.1 region has been reported to be related with chromosome instability. A complete physical map, which covers the 3.2 Mb region of 16q23.3 - 24.1 (D16S402 and D16S486), was constructed to identify novel candidate tumor suppressor genes. We provide the minimally tiling path map consisting of 28 BAC clones. There was one gap between NT_10422.11 and NT_019609.9 of the human genome sequence contig (NCBI sequence build 33, April 29, 2003). This gap can be filled by sequencing the R-1425M20 clone which bridges these sequence contigs.

스핀 코팅법으로 증착한 (Bi1La1)4Ti3O12 박막의 후속 열공정에 따른 입자 크기 및 결정 방향성 변화 (Thermal Process Effects on Grain Size and Orientation in (Bi1La1)4Ti3O12 Thin Film Deposited by Spin-on Method)

  • 김영민;김남경;염승진;장건익;류성림;선호정;권순용
    • 한국전기전자재료학회논문지
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    • 제20권7호
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    • pp.575-580
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    • 2007
  • A 16 Mb 1T1C FeRAM device was integrated with BLT capacitors. But a lot of cells were failed randomly during the measuring the bit-line signal distribution of each cell. The reason was revealed that the grain size and orientation of the BLT thin film were severely non-uniform. And the grain size and orientation were severely affected by the process conditions of post heat treatment, especially nucleation step. The optimized annealing temperature at the nucleation step was $560^{\circ}C$. The microstructure of the BLT thin film was also varied by the annealing time at the step. The longer process time showed the finer grain size. Therefore, the uniformity of the grain size and orientation could be improved by changing the process conditions of the nucleation step. The FeRAM device without random bit-fail cell was successfully fabricated with the optimized BLT capacitor and the sensing margin in bit-line signal distribution of it was about 340 mV.

Lipoteichoic Acid Isolated from Lactobacillus plantarum Maintains Inflammatory Homeostasis through Regulation of Th1- and Th2- Induced Cytokines

  • Ahn, Ji Eun;Kim, Hangeun;Chung, Dae Kyun
    • Journal of Microbiology and Biotechnology
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    • 제29권1호
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    • pp.151-159
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    • 2019
  • Lipoteichoic acid isolated from Lactobacillus plantarum K8 (pLTA) alleviates lipopolysaccharide (LPS)-induced excessive inflammation through inhibition of $TNF-{\alpha}$ and interleukin (IL)-6. In addition, pLTA increases the survival rate of mice in a septic shock model. In the current study, we have found that pLTA contributes to homeostasis through regulation of pro- and anti-inflammatory cytokine production. In detail, pLTA decreased the production of IL-10 by phorbol-12-myristate-13-acetate (PMA)-differentiated THP-1 cells stimulated with prostaglandin E2 (PGE-2) and LPS. However, $TNF-{\alpha}$ production which was inhibited by PGE-2+LPS increased by pLTA treatment. The regulatory effects of IL-10 and $TNF-{\alpha}$ induced by PGE-2 and LPS in PMA-differentiated THP-1 cells were mediated by pLTA, but not by other LTAs isolated from either Staphylococcus aureus (aLTA) or L. sakei (sLTA). Further studies revealed that pLTA-mediated IL-10 inhibition and $TNF-{\alpha}$ induction in PGE-2+LPS-stimulated PMA-differentiated THP-1 cells were mediated by dephosphorylation of p38 and phosphorylation of c-Jun N-terminal kinase (JNK), respectively. Reduction of pLTA-mediated IL-10 inhibited the metastasis of breast cancer cells (MDA-MB-231), which was induced by IL-10 or conditioned media prepared from PGE-2+LPS-stimulated PMA-differentiated THP-1 cells. Taken together, our data suggest that pLTA contributes to inflammatory homeostasis through induction of repressed pro-inflammatory cytokines as well as inhibition of excessive anti-inflammatory cytokines.

마늘추출물에 의한 암세포의 이동 저하 (Inhibition of Cancer Cell Migration by Compounds from Garlic Extracts)

  • 김은경;윤성지;하정민;진인혜;김영환;김선근;박다정;최영환;윤식;김치대;배순식
    • 생명과학회지
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    • 제21권6호
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    • pp.767-774
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    • 2011
  • 세포의 이동은 많은 생리적 반응뿐만 아니라 암 세포 침윤과 전이에 중요한 역할을 수행한다. 본 연구에서는 마늘이 암세포의 이동에 미치는 영향을 확인하기 위해, 표준 마늘과 흑마늘을 준비하고 이들을 각각 물을 이용하여 추출하거나 건조하여 추출한 추출물 4 종류를 이용하여 항침윤성과 항전이성에 대해 조사하였다. 실험결과, 암세포의 이동은 건조 후 헥산으로 추출한 분획에 암세포의 이동 억제 활성이 관찰되었다. 이 분획을 박막 크로마토그래피를 이용하여 분리정제하였으며, 이를 inhibitor of cancer metastasis from garlic #27 (ICMG-27)이라 명명하였다. ICMG-27 (6 ${\mu}g/ml$)을 세포에 처리하였을 때, IGF-1에 의한 OVCAR-3와 NIH-3T3 세포의 이동을 억제함을 확인하였다. 그러나 ICMG-27은 mouse embryonic fibroblast (MEF) 세포에서 IGF-1에 의한 이동에는 영향을 주지 않았다. 이러한 ICMG-27은 OVCA-3, SKOV-3와 MDA-MB-231 세포와 같은 암세포에서 모두 IGF-1에 의한 이동을 억제함을 관찰하였다. 마지막으로 세포이동을 일으키는 인자에 따른 ICMG-27의 영향을 확인한 것으로, IGF-1, lysophosphatidic acid (LPA), sphingosine-1-phosphate (S1P), leukotriene B4 (LTB4) 그리고, angiotensinII (AngII)에 의한 OVCAR-3 세포의 이동을 모두 억제하였다. 이러한 결과를 바탕으로, ICMG-27은 암세포의 이동을 유도하는 많은 인자들에 의한 필수적인 단계를 차단함으로써, 암세포의 이동을 억제하는 것을 확인 할 수 있었으며, ICMG-27에 의한 암세포의 항 침윤 메커니즘의 규명은 암환자의 치료에 기초적인 발판을 제공할 것입니다.

흑마늘과 쑥 추출물이 구속스트레스를 가한 흰쥐의 체내 지질 성분에 미치는 영향 (Effect of Black Garlic and Mugwort Extracts on Lipids Profile during Restraint Stress)

  • 이수정;강민정;신정혜
    • 한국식품영양과학회지
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    • 제42권4호
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    • pp.577-586
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    • 2013
  • In vitro에서 흑마늘과 쑥 추출분말 및 이들의 비율별 혼합물 3종(MPA, 95:5; MPB, 90:10; MPC, 85:15, w/w%)의 생리활성을 비교하였다. 또한 7 brix 흑마늘 추출물(BE), 0.7 brix 쑥 추출물(ME), 이들을 부피비로 95:5(MA), 90:10(MB) 및 90.25:4.75 혼합물에 사과 추출물과 자일리톨을 각각 2%와 3%를 첨가한 음료(MC)를 흰쥐에게 4주간 급이한 후 24시간 구속스트레스를 부과하여 생체내 지질 성분 변화에 미치는 영향을 평가하였다. In vitro에서 흑마늘 추출물과 쑥 추출물의 혼합물(MPA, MPB, MPC)은 쑥 추출물의 첨가량이 증가됨에 따라 DPPH 및 ABTS 라디칼 소거활성이 유의적으로 증가하였다. 흑마늘 추출물(RS1), 쑥 추출물(RS2), 혼합물 MA(RS3), MB(RS4) 및 MC(RS5)를 각각 1%씩 흰쥐의 식이에 첨가 급이한 결과 식이섭취량은 RS1군에서 가장 높았으며, 체중 증가량과 식이효율은 실험군 간에 유의차가 없었다. 혈청의 총 콜레스테롤의 함량은 구속 대조군(RSC군)에 비해 모든 실험군에서 유의적으로 낮은 함량이었으며, RS3~RS5군 간에는 유의차를 보이지 않았다. 혈중 중성지질의 함량은 RS3~RS5군이 RS1과 RS2군보다 유의적으로 높은 수준이었다. HDL-C 및 LDL-C 함량, 동맥경 화지수(AI), 심혈관질환 위험지수(CRF)는 RS3~RS5군 간에 유의차가 없었다. AST 및 ALP 활성은 RSC군에 비해 실험군들에서 유의적으로 낮았다. 간 조직의 총 지질과 총 콜레스테롤 함량은 RSC군에 비해 모든 실험군에서 유의적으로 낮았고, 중성지방 함량은 RS1군만이 유의적으로 낮은 함량이었다. 간 글리코겐 함량은 RSC군에 비해 RS2와 RS3군이 유의적으로 높았고, 그 외 실험군에서는 유의차가 적었다. 지질과산화물 함량은 RSC군에 비해 실험군에서 유의적으로 낮았으며, RS3과 RS5군이 유사한 수준이었다. 본 연구결과에서 흑마늘 추출물, 쑥 추출물, 혼합물 및 개발 음료의 급이는 스트레스 부과로 증가될 수 있는 체내 지질 수준의 감소에 효과적이었다. 또한 각 물질의 단독 급이보다 혼합물의 급이시 더 효과적인 것으로 나타나 혼합물을 이용한 개발음료는 현대인의 복잡하고 다양한 스트레스 발생 시 생체대사 조절에 도움이 될 것으로 사료된다.

인체에 적용한 전기자극이 Serum myoglobin과 Aldolase에 미치는 영향에 대한 생리학적 효과 (A experimental study on the physiological effects of electrical stimulation treatment of serum myoglobin and aldolase in human body)

  • 김순희;천기영;최영덕
    • 대한물리치료과학회지
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    • 제6권3호
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    • pp.53-61
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    • 1999
  • Prior studies have revealed that several stimulation to the muscle have released serum myoglobin into the blood vessel and increased aldolase activity. The present authors carried out a study which effect of electrical stimulation treatment (induced a isotonic wrist exerceise) on serum myoglobin(Mb) levels and aldolase(Al) activity were investigated in 6 healthy female. There were four groups of female: 1. no electrical stimulation control: 2. electrical stimulation 10min (EST10'); 3. electrical stimulation 20 min (EST20'); 4. electrical stimulation 30min (EST30'). Each groups is all the same one. Radioimmunoassay and Ultraviolet Spectrophotometry were performed to increased or decreased of serum myoglobin and aldolase. Serum myoglobin significantly increased in electrical stimulated groups[EST10' $(30.20{\pm}5.27ng/ml)$, EST20'$(31.65{\pm}3.96ng/ml)$, EST30'$(31.95{\pm}2.0ng/ml)$] to be compared with control group$(24.43{\pm}2.20ng/ml)$. Aldolase significantly increased in electrical stimulated groups [EST10' ($6.85{\pm}1.17$ Sigma U/mL), EST20'($6.70{\pm}1.46$ Sigma U/mL), EST30'($6.56{\pm}1.01$ Sigma U/mL)) to be compared with control group($5.03{\pm}1.86$ Sigma U/mL). The results of this study show that isotonic exercise result in electrical stimulation treatment increased serum myoglobin content and aldolase activity. In conclusion, our results support that stimulation release serum myoglobin and increase aldolase activity.

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