Oral squamous cell carcinoma is the 1st most common malignancy in oral and maxillofacial area. HPV 16 has been strongly linked to progression of cervical carcinoma. E6 and E7 as a small DNA virus encoding two major oncoproteins of HPV 16 can act together to produce efficient immortalization of primary human epithelial cells. Thus it is important to pursue the development of Immortalized human oral keratinocyte(IHOK) culture model which could be related to the pathogenesis of oral squamous cell carcinoma. If we establish IHOK transfected by E6/E7 genes, IHOK will be accepted as a model system for HPV-linked oral carcinogenesis. The purpose of this study were to culture primary normal human oral keratinocyte(NHOK), and to establish IHOK for studying oral carcinogenesis in the future. NHOK was primarily cultured under normal culture condition, and transformed into IHOK by transfection of E6/E7 genes. After 100 passages depend on Ca++ condition, cultured IHOK was confirmed by growth curve, cornified cell envelope measurement, TGase 1activity, mRNA detection, tumorogenecity and anchorage independence assay. After 100 passages, cultured IHOK showed most basal cell and monolayer of polyhedral cells under 0.15mM Ca++, and small area of stratification and flattened epithelial cells with irregular border under 1.2mM Ca++. The cultured IHOK showed relatively resistant growth under high calcium condition. The E6/E7 mRNA was detected in cultured IHOK by RT-PCR. During the terminal differentiation in cultured IHOK, increased insoluble cornified cell envelope formation was accompanied with induction of TGase 1 activity. But the cultured IHOK showed less CEM and TGase 1 activity than those of cultured NHOK. Cultured IHOK showed non-tumorogenecity, but slight anchorage independence. We had developed a technique to transform NHOK into IHOK by transfection of E6/E7 genes. Cultured IHOK was established as intermediate stage cell to study the pathogenesis of human oral squamous cell carcinoma.

Cultured normal human oral kera tinocyte(NHOK) & inunortalized human oral keratinocyte(IHOK) provide a valuable model in ce llular proliferation and differentiation after proper stimulation , And it is interesting to study these estab lished cell lines esca ping normal control on their growth and differentiation, SPRR1 is induced during t erminal differ entiation 0 1' human epiderma l kerat inocytes but is rarely in anaplastic cells of keratinocyte origin, But SPR1 expression has not yet been explained during differ entiation uf NHOK and Lransformed oral keraLinocyLes , The purpose of this study were to examine mHNA and protein expression of SPR1 in response to a known differentiation signal, calcium conc in NHOK, lHOK a nd oral SCC ce ll line(HN 4) , and to apply these results for investigating the molecular mecha nisms of tra nsformed cellular differentiation , Primary cultured NHOK, established IHOK and HN 4 cell line were cul tured in KBM bullet kit Preconfluency of NHOK as control group was used Under O, 15mM Ca++ conc(Precon, Postcon) , and 1, 2mM Ca++ conc(Pos tcon)‘ the insoluble final pellets were measured fo1' cornified cell envelope measurements, and RT- PCR for SPRR1 mRNA meas urement, and immunoblotting for SPRR1 protein measurements in tripli cate , resp ectively , The terminal different ia tion of cu ltured NHOK and IHOK was depend on calcium concentration, while HN4 cell line was not SPRR1 mRNA and protein expression of cultured NHOK showed the highest among cultured IHOK & HN 4 cell line in hi gher ca lcium condition , SPRR1 mRNA and protein expression of cultured IHOK showed higher‘ than tha t of HN 4 cell line in hjgher cacium condi tion , SPRH1 was expressed in differentiation of NHOK and IHOK t ransfected by E6/E7 genes but ra rely expressed in malignant oral keratinocytes , It suggested that SPRR1 ex pression as kera tinocyte terminal diff‘erent ia tion marker involved in cellular cornification would be differentially effected by immorta li zation and ca rcinogenic transforma tion

It is well kwon that HPV have been strongly linked to progression of or al squamous cell carcinoma‘ Effici ent im mortalization of nonnal human oral keratinocyte(NHOK) should provid further evidence for the role HPV in tumorogenes is ‘ Because IHOK(I mmortali zed human oral keratinocyte) has been considered as a moclel syst em for study ing I-!PV- linkecl oral ca rcinogenes is , it is important to pursue the differenti ati al change of IHOK cul t ure moclel during t he culture passage, The purposes of this study were to examine the cha ra r’ ct eristic clifferential changes of cul turecl immorta lizecl human ora l keratinocytes during long term passage, and to apply these results to or al carcinogenes is in the future, NI-!OK was primarily incubated at 370C and 5% C02 under KBM bullet kJt IHOK was co ntinuously cul t ured towarcl 100th passage(two times per week) , Growth curve of NI-!OK and II-!OK clepend on clùture passage was taken For examining the cha racte ri s t ic clifferential changes of II-!OK, transrnission electron microscope, 1ì'ansgluta miase activity‘ E6/E7 mRNA detect ion, a ncl tumorogenecity were done 10th II-!OK showecl sl ight polygonal flattencl cells and sometimes apoptotic cells ‘ while 100th IHOK showecl increased polygonal cell s ‘ Cultu recl 100th IHOK showed r ela tively resis tant growth to high calcium than 10th II-!OK Microvilli from 10th II-!OK was not connect ecl with each other, ancl scatte red cytokeratin fil aments of 10th II-IOK. while decreased cytokeratin filaments in cytoplasm & prominent clesmosome of 100th IHOK. During the terminal differ entiation in cultured IHOK, induction of TGase 1 activity of 10th II-!OK was higher than that of100th IHOK mRNA E6E7 expresson was cletected and unchangable in both cul tured cells There was no tumorogenecity inclucecl by both culturecl cel ls. Although late passage IHOK showecl less r esemblance to NHOK, and lower TGase 1 acti vi ty than ea rly passage IHOK, it suggested that these cells should be 110t yet fully differ entiatecl to oral squ a mous ce ll carcinoma cells

Abnormal number of deciduous teeth causes esthetic and dental problems on infants or children, which has effect on articulation disorder and emotional development as well as their physical growth. Therefore, it is important to detect dental problems early and to provide comparable indications. The purose of this study was to find out the prevalence and pattern in abnormal number of deciduous teeth. The clinical and radiographic examination was undertaken for 200 at age from 1 to 10 years and statistical analysis was done. The result were as follows. Among the examined patients, congenital missing teeth 8.6% and supernumerary teeth 36.4% were seen(p<0.05). And abnormal number of deciduous teeth was prevalent in male. Most supernumerary teeth located on middle area(88.6%) was seen(p<0.05). The most frequently missing teeth was the mandibular primary lateral incisor and the mandibular 2nd. premolar. And these teeth were mainly located in maxilla and right portion. It suggested that this study would play an important role for the basis of the demographic research of abnormal teeth in oral pathologic field

It is very little known that the molecular mechanisms control growth, cell differentiation, and invasion of ameloblastoma into bone. Tissue culture methods have also been used extensively for studies of the cell biology of ameloblastoma. The purpose of this study were to examined the ultrastructural features of ameloblastoma, and to apply these results to examine the pathogenesis of ameloblastoma in the future. Amelobalstoma was primarily cultured under 0.1, 0.15 and 1.2mM Ca++ of KBM bullet kit at 370C and 5% C02. For transmission electronmicroscopy(TEM), cultured ameloblastoma cells were immediately fixed in 2.0% glutaraldehyde in O.lM cacodylate buffer(pH 7.4) at 40C for 1h The ultrathin sections were stained with uranyl acetate and lead citrate, and examined by TEM. The obtained results were as follows. Primay culture ameloblastoma grown in 0.1 mM Ca++ showed interlacing papillary projections without desmosome within early passage(3-4). Primary culture amelobalstoma under high calcium showed prominent desmosomes or tight junctions within early passage. There was evidence of cellular degeneration, as exemplified by nuclear pyknosis, the margination and clumping of the chromatin, and vaculolation under high calcium. The sparse ribosomes, the cytoplasmic space filled with vacuoles, and the condensed mitochondria were seen under high calcium. From the aboving results, under high calcium primary culture ameloblastoma showed rapid cellular degeneration within early passage, indicating that the cells were gradually losing metabolíc actívitíes, leading to enventual cell death. It was thought that it would be necessary to establish cultured immortalized amelobalstoma cell line for studying the pathogenesis of odontogenic tumors.

The study of cornified cell envelope has been used to investigate the differentiation factors and to advance oral carcinogenesis, CE of human oral keratinocytes are in wet condition as saliva containing many proteases, growth factors, and many kinds of bacteria, The analysis of CE in Immortalized human oral keratinocyte(IHOK) derived from normal human oral keratinocyte(NHOK) will be used to study the pathogenesis of oral squamous cell carcinoma, The purpose of this study was to analyze the amino acid component derived from CE of cultured NHOK and IHOK, It will be helpful to study the role of transfected E6/E7 gene in forming CE, and to examine the pathogenesis of oral squamous cell carcinoma, After primry culture of NHOK, IHOK were cultured in KBM bullet kit at 370C under 95% C02 incubator, Growth curve according to calcium concentration, cornified cell envelope measurement(CEM), and protein chemistry for amino acid component of CE were done(Mena :f::SD) , respectively. The obtained results were as follows, lHOK showed small areas of stratification, more compact, with irregular border and tightly apposed cells in 1,2 mM Ca++, Cornified cell envelope exhibited an aggregated group of empty space surrounded by the remained cell membrane, During the terminal differentiation in cultured NHOK and IHOK, insoluble cornified cell envelope formation was increased, CEM of NHOK was about 4 folds than that of lHOK under high calcium, Amino acid component of both groups showed Pro/Glu(SPR) , Gln/Glu(lnvolucrin) , and Gly(Loricrin) in descending order, From the aboving results, ít was suggested that when the terminal dífferentiation in cultured NHOK and IHOK, major amino acid component of CE in cultured lHOK was the same to that of cultured NHOK, It was thought that E6 and E7 gene should be involved in preventing the differentiation and proliferation of IHOK from making CE,

The impact of sound speed variability in the sea is the very important on acoustic propagation for the underwater acoustic systems. Understanding of the temporal and spatial variability of ocean sound speed in the sea around the Ieodo were obtained using oceanographic data (temperature, salinity). from the Korea Oceanographic Data Center, collected by season for 17 years. The vertical distributions of sound speed are mainly related to seasonal variations and various current such as Chinese coastal water, Yellow Sea Cold Water (YSCW), Kuroshio source water. The standard deviations show that great variations of sound speed exist in the upper layer and observation station between 16 and 18. In order to quantitatively explain the reason for sound speed variations, Empirical Orthogonal Function (EOF) analysis was performed on sound speed data at the Line 316 covering 68 cruises between 2002 and 2018. Three main modes of EOFs respectively revealed 55, 29, and 5% the total variance of sound speed. The first mode of the EOFs was associated with influence of surface heating. The second EOFs pattern shows that contributions of YSCW and surface heating. The first and second modes had seasonal and inter-annul variations.

폐기물 해양투기 방지를 위한 국제협약인 런던협약･의정서에 따라 2012년 가축분뇨의 해양배출이 전면금지 되었으며, 국내 가축분뇨 발생량은 2011년 128,621 ㎥/일에서 2014년 175,651 ㎥/일로 점차 증가하고 있는 실정이다. 또한 가축분뇨를 육상처리 시 발생하는 메탄가스로 인한 악취문제나 처리되지 못한 영양염류 및 고농도의 유기물이 하천으로 배출되어 부영양화를 일으키는 등의 문제가 대두되고 있다. Biochar는 혐기성 상태의 환경에서 분뇨와 같은 바이오매스를 열분해 시켜 생성한 고형물질이다. 최근 연구에 따르면 Biochar를 토양에 적용할 경우 주변의 이산화탄소를 장기간 저장하고 중금속을 흡착하며 토양 내 수분보유능력을 증가시키는 등 친환경 소재로써의 가치가 평가되고 있다. 따라서 본 연구에서는 수분함량이 높아 재활용이 어려운 가축분뇨를 열수가압탄화반응(Hydrothermal Cabonization, HTC)방법으로 Biochar를 제조하여, 중금속 흡착제로서의 사용가능성을 평가하고자 하였다. Biochar는 Stainless재질의 500 mL 용량의 반응기를 사용하였으며 온도, 반응시간, 입경에 따른 생성수율을 도출하고 각각의 원소분석, 삼성분 및 중금속 함량분석 등의 물리·화학적분석을 통한 특성분석을 수행하였다. 이 결과 원료와 비교하여 Biochar의 탄소성분은 약 25 % 증가했고 중금속 함량은 감소하는 경향을 보였다. 또한 흡착능력을 알아보기 위해 요오드 흡착성능을 분석한 결과, 원료 대비 약 52.4 %의 흡착성능 증가를 확인하였다.

본 논문에서는 장면에 어울리도록 유체를 카툰 스타일로 표현할 수 있는 실시간방법을 제안하고자 한다. 실제로 유체는 석양, 낮, 밤에 서로 다른 색상 톤을 보여주고 있고 수심이 낮은 곳에서의 반사 굴절 정도와 수심이 깊은 곳에서의 정도가 상이하며 색상 조차 다르다. 본 논문에서는 광원 수심 지형 시점 등에 적응적으로 유체를 카툰 스타일로 표현하는 방식을 제안한다. 실험은 기존의 방법을 구현하고 제안된 결과와 비교 분석하였다. 이러한 연구는 기존의 카툰 스타일렌더링 방법과 제안하는 카툰 스타일 방법과 동시에 사용하면 게임을 카툰 스타일로 표현할 수 있는 전체 시스템을 제시할 수 있다.

본 연구는 게임 물리 엔진을 실시간 물리 기술의 관점으로 고찰한다. 실시간 물리 기술이란 물리 시뮬레이션 기술을 게임에 적용하기 위해서 간략화 하는 기술을 말한다. 조사 대상으로 상용 물리 엔진인 Havok Physics SDK와 NVIDIA PhysX SDK를 선택하였고, 오픈 소스기반 물리 엔진인 ODE와 Bullet을 선택하였다. 그 결과 물리 엔진은 강체 역학, 변형체 시뮬레이션, 유체 시뮬레이션을 구현하고 있었고, 실시간 시뮬레이션을 위해서 수식의 간략화, 충돌 처리의 효율성 재고 등 소프트웨어 측면의 기술과 멀티 코어 CPU의 이용, PPU, GPU 활용 등 병렬처리 하드웨어 기술을 사용하고 있었다.