• 호남수학학술지
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• 제39권4호
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• pp.655-663
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• 2017

In this paper we define $AP_c$ and $AP_{cc}$ spaces which are stronger than the property of approximation by points(AP). We investigate operations on their subspaces and study function theorems on $AP_c$ and $AP_{cc}$ spaces. Using those results, we prove that every continuous image of a countably compact Hausdorff space with AP is AP. Finally, we prove a theorem that every compact ${\kappa}$-WAP space is ${\kappa}$-pseudoradial, and prove a theorem that the product of a compact ${\kappa}$-radial space and a compact ${\kappa}$-WAP space is a ${\kappa}$-WAP space.

• Molecules and Cells
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• 제19권3호
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• pp.452-457
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• 2005

The adaptor protein (AP) complexes are involved in membrane transport of many proteins. There are 3 AP complexes in C. elegans unlike mammals that have four. To study the biological functions of the AP-3 complexes of C. elegans, we sought homologues of the mouse and human genes that encode subunits of the AP-3 complexes by screening C. elegans genomic and EST sequences. We identified single copies of homologues of the ${\mu}3$, ${\sigma}3$, ${\beta}3$ and ${\delta}$ genes. The medium chain of AP-3 is encoded by a single gene in C. elegans but two different genes in mammals. Since there are no known mutations in these genes in C. elegans, we performed RNAi to assess their functions in development. RNAi of each of the genes caused embryonic and larval lethal phenotypes. APM-3 is expressed in most cells, particularly strongly in spermatheca and vulva. We conclude that the products of the C. elegans ${\mu}3$, ${\sigma}3$, ${\beta}3$ and d genes are essential for embryogenesis and larval development.

• 약학회지
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• 제43권1호
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• pp.42-47
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• 1999

Phorbol ester, growth factors activities are mediated by unclear transcription factors, the c-Fos and c-Jun, which can regulate transcriptional activation through specific DNA sites and by forming the transcription factor AP-l, which usually mediates cell proliferation and differentiation signals. We explored effects of Pini Folium extract (API-l) on AP-l activity. Western blot analysis confirmed that API-l decreased levels of c-Fos or c-Jun protein induced by the tumor promoter Phorbol 12-myristate 13-acetate (PMA; 200 nM). Transient transfection assays with a c-fos promoter reporter construct showed that API-l decreased transcription activity by ore than 50~60%. However, treatment of API-l activity studied further. The main substances were fractionated into dichloromethane layer. Futhermore, API-l extract repressed the [$^3H$]-thymidine uptake in C6 glioma cells, indicating that this extract could be included in a new type of modulator in the mitogenesis.

• 정보처리학회논문지C
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• 제17C권6호
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• pp.491-498
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• 2010

Wi-Fi 기반의 차량과 기지국간 (vehicle-to-infrastructure, V2I) 통신은 차량과 승객의 안전과 편의 및 교통 효율성을 향상시킬 수 있는 방법으로 관심을 받고 있다. 그러나 노변에 위치한 엑세스 포인터 (access point, AP)는 이동차량에게 비용적인 측면에서 효과적인 인터넷 연결을 지원할 수 있지만, 차량의 빠른 이동과 AP의 제한된 전송거리는 빈번한 핸드오프를 유발한다. 그러한 문제점은 모바일 AP (mobile AP, MAP) 플랫폼을 사용하여 해결할 수 있다. MAP는 노변에 위치한 AP보다 적은 양의 대역폭을 제공하지만, 차량과 함께 이동함에 따라 더 오랜 시간 서비스를 제공할 수 있다. 이 논문은 이동차량이 노변의 고정된 AP 혹은 MAP 중에서 효과적으로 AP를 선택할 수 있는 하나의 새로운 AP 선택 기법을 제안한다. AP 선택기준을 위하여 AP의 접속 가용시간과 제공 가능 대역폭을 함께 고려하고, 그러한 기준을 바탕으로 AP 선택 기법을 제안한다. 실제 버스 트레이스 기반의 시뮬레이션을 통해 제안한 기법이 기존의 방법보다 좋은 성능을 제공하는 것을 보여준다.

• The Korean journal of internal medicine
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• 제33권6호
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• pp.1103-1110
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• 2018

Background/Aims: Several epidemiological studies have validated the association of interleukin gene polymorphisms with acute pancreatitis (AP) in different populations. However, there have been few studies in Asian ethnic groups. We aimed to investigate the relationships between inflammatory cytokine polymorphisms and AP as pilot research in a Korean ethnic group. Methods: Patients who had been diagnosed with AP were prospectively enrolled. DNA was extracted from whole blood, and DNA sequencing was subsequently performed. Single-nucleotide polymorphisms (SNPs) of the interleukin $1{\beta}$ (IL1B), interleukin 1 receptor antagonist (IL1RN), and tumor necrosis factor ${\alpha}$ (TNFA) genes of patients with AP were compared to those of normal controls. Results: Between January 2011 and January 2013, a total of 65 subjects were enrolled (40 patients with AP vs. 25 healthy controls). One intronic SNP (IL1RN -1129T>C, rs4251961) was significantly associated with the risk of AP (odds ratio, 0.304; 95% confidence interval, 0.095 to 0.967; p = 0.043). However, in our study, AP was not found to be associated with polymorphisms in the promoter regions of inflammatory cytokine genes, including IL1B (-118C>T, c47+242C>T, +3954C/T, and -598T>C) and TNFA (-1211T>C, -1043C>A, -1037C>T, -488G>A, and -418G>A). Conclusions: IL1RN -1129T>C (rs4251961) genotypes might be associated with a significant increase of AP risk in a Korean ethnic group.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 1994년도 제2회 학술강연회논문집
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• pp.23-26
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• 1994

130mm D.B. 추진기관의 고온 시험에서 나타난 극심한 이상 연소 현상을 해결하기 위해 미세한 고체 입자들을 연소 가스에 분산시켜 불안정 연소를 억제하는 particulate damping 효과를 연구하였다. 고체 입자로서 효과적인 것으로 알려진 $K_2$$SO_4$. ZrC, Graphite를 CTPB, HTPB 고분자 물질에 충진시켜 epoxide, isocyanate 반응기와 가교 반응을 일으킴으로써 고무상의 탄성체 성질을 갖게 하는 $K_2$$SO_4$/CTPB, ZrC/Graphite/HTPB, ZrC/Graphite/AP/HTPB, ZrC/AP/HTPB 조성의 연소 안정제를 개발하였다. 이 연소 안정제는 외경 17mm, 길이 1000mm의 안정봉 형태로 제작하여 모타의 중심 cavity에 조립한 후 지상 연소 시험을 통하여 성능을 확인하였다. 시험 결과, 조성에 AP를 포함시켜 연소 안정제에 일정한 연소 속도를 부여하여 추진제 grain 연소 동안 고체 입자를 연소 가스에 분산되게 설계한 ZrC/Graphite/AP/HTPB, ZrC/AP/HTPB 조성의 연소 안정제가 불안정 연소 억제에 효과적인 것으로 나타났다.

• 융합정보논문지
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• 제7권6호
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• pp.89-95
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• 2017

암을 유발하는 PMA는 세포를 자극하여 전사인자 C-Jun/C-fos의 발현을 증가시키며 핵 내의 AP-1의 활성을 증가하게 되고 결과적으로 각종 암이 발생된다고 보고되고 있다. 본 연구에서는 천연물 지표성분의 안전성을 보기위한 세포독성과 암예방 효과를 예측할 수 있는 Activator protein(AP-1) 활성억제를 관찰하였다. 천연물 지표성분 38종을 대상으로 세포독성과 AP-1 활성억제를 관찰한 결과 섬수의 지표성분인 Bufogein 과 Cinobufagin에서는 세포독성을 보이며 AP-1 활성 억제와 비교 시 5배 정도 차이를 보임을 알 수가 있다. 반면에 Arctigenin, Manassantin A, B에서는 AP-1 활성 억제 농도는 $2{\mu}M$ 이하이면서 세포독성과의 비율은 15배 이상임을 알 수 있다. 본 실험의 결과를 통해 우방자와 삼백초의 지표성분인 Arctigenin, Manassantin A,B는 암 예방 연구의 가능성을 시사하였다.

• IMMUNE NETWORK
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• 제10권2호
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• pp.35-45
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• 2010

Background: Expression of recombinant antibodies and their derivatives fused with other functional molecules such as alkaline phosphatase in Escherichia coli is important in the development of molecular diagnostic reagents for biomedical research. Methods: We investigated the possibility of applying a well-known Fos-Jun zipper to dimerize $V_H$ and $V_L$ fragments originated from the Fab clone (SP 112) that recognizes pyruvate dehydrogenase complex-E2 (PDC-E2), and demonstrated that the functional zipFv-112 and its alkaline phosphatase fusion molecules (zipFv-AP) can be produced in the cytoplasm of Origami(DE3) trxB gor mutant E. coli strain. Results: The zipFv-AP fusion molecules exhibited higher antigen-binding signals than the zipFv up to a 10-fold under the same experimental conditions. However, conformation of the zipFv-AP seemed to be influenced by the location of an AP domain at the C-terminus of $V_H$ or $V_L$ domain [zipFv-112(H-AP) or zipFv-112(L-AP)], and inclusion of an AraC DNA binding domain at the C-terminus of VH of the zipFv-112(L-AP), termed zipFv-112(H-AD/L-AP), was also beneficial. Cytoplasmic co-expression of disulfide-binding isomerase C (DsbC) helped proper folding of the zipFv-112(H-AD/L-AP) but not significantly. Conclusion: We believe that our zipFv constructs may serve as an excellent antibody format bi-functional antibody fragments that can be produced stably in the cytoplasm of E. coli.

• Molecules and Cells
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• 제28권2호
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• pp.87-92
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• 2009

Human SIRT3 gene contains an intronic VNTR enhancer. A T > C transition occurring in the second repeat of each VNTR allele implies the presence/absence of a putative GATA binding motif. A partially overlapping AP-1 site, not affected by the transition, was also identified. Aims of the present study were: 1) to verify if GATA and AP-1 sites could bind GATA2 and c-Jun/c-Fos factors, respectively; 2) to investigate whether such sites modulate the enhancer activity of the SIRT3-VNTR alleles. DAPA assay proved that GATA2 and c-Jun/c-Fos factors are able to bind the corresponding sites. Moreover, co-transfection experiments showed that the over-expression of GATA2 and c-Jun/c-Fos factors boosts the VNTR enhancer activity in an allelic-specific way. Furthermore, we established that GATA2 and c-Jun/c-Fos act additively in modulating the SIRT3-VNTR enhancer function. Therefore, GATA2 and AP-1 are functional sites and the T > C transition of the second VNTR repeat affects their activity.

• Journal of Ginseng Research
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• 제39권2호
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• pp.155-161
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• 2015

Background: Korean ginseng is an ethnopharmacologically valuable herbal plant with various biological properties including anticancer, antiatherosclerosis, antidiabetic, and anti-inflammatory activities. Since there is currently no drug or therapeutic remedy derived from Korean ginseng, we developed a ginsenoside-enriched fraction (AP-SF) for prevention of various inflammatory symptoms. Methods: The anti-inflammatory efficacy of AP-SF was tested under in vitro inflammatory conditions including nitric oxide (NO) production and inflammatory gene expression. The molecular events of inflammatory responses were explored by immunoblot analysis. Results: AP-SF led to a significant suppression of NO production compared with a conventional Korean ginseng saponin fraction, induced by both lipopolysaccharide and zymosan A. Interestingly, AP-SF strongly downregulated the mRNA levels of genes for inducible NO synthase, tumor necrosis factor-${\alpha}$, and cyclooxygenase) without affecting cell viability. In agreement with these observations, AP-SF blocked the nuclear translocation of c-Jun at 2 h and also reduced phosphorylation of p38, c-Jun N-terminal kinase, and TAK-1, all of which are important for c-Jun translocation. Conclusion: Our results suggest that AP-SF inhibits activation of c-Jun-dependent inflammatory events. Thus, AP-SF may be useful as a novel anti-inflammatory remedy.