• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제30권6호
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• pp.465-473
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• 2004

Purpose : The essential triad for nerve regeneration is nerve conduit, supporting cell and neurotrophic factor. In order to improve the peripheral nerve regeneration, we used polyglycolic acid(PGA) tube and brain-derived neurotrophic factor(BDNF) gene transfected Schwann cells in sciatic nerve defects of SD rat. Materials and methods : Nerve conduits were made with PGA sheet and outer surface was coated with poly(lactic-co-glycolic acid) for mechanical strength and control the resorption rate. The diameter of conduit was 1.8mm and the length was 17mm Schwann cells were harvested from dorsal root ganglion(DRG) of SD rat aged 1 day. Schwann cells were cultured on the PGA sheet to test the biocompatibility adhesion of Schwann cell. Human BDNF gene was obtained from cDNA library and amplified using PCR. BDNF gene was inserted into E1 deleted region of adenovirus shuttle vector, pAACCMVpARS. BDNF-adenovirus was multiplied in 293 cells and purified. The BDNF-Adenovirus was then infected to the cultured Schwann cells. Left sciatic nerve of SD rat (250g weighing) was exposed and 14mm defects were made. After bridging the defect with PGA conduit, culture medium(MEM), Schwann cells or BDNF-Adenovirus infected Schwann cells were injected into the lumen of conduit, respectively. 12 weeks after operation, gait analysis for sciatic function index, electrophysiology and histomorphometry was performed. Results : Cultured Schwann cells were well adhered to PGA sheet. Sciatic index of BDNF transfected group was $-53.66{\pm}13.43$ which was the best among three groups. The threshold of compound action potential was between 800 to $1000{\mu}A$ in experimental groups which is about 10 times higher than normal sciatic nerve. Conduction velocity and peak voltage of action potential of BDNF group was the highest among experimental groups. The myelin thickness and axonal density of BDNF group was significantly greater than the other groups. Conclusion : BDNF gene transfected Schwann cells could regenerate the sciatic nerve gap(14mm) of rat successfully.

• Asian Pacific Journal of Cancer Prevention
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• 제16권18호
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• pp.8653-8658
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• 2016

Background: Heparanase is believed to be involved in gastric carcinogenesis. However, the clinicopathologic features of gastric cancer with high heparanase expression remain unclear. Aim : The purpose of this study was to comprehensively and quantitatively summarize available evidence for the use of heparanase mRNA and protein expression to evaluate the clinicopathological associations in gastric cancer in Asian patients by meta-analysis. Materials and Methods: Relevant articles listed in MEDLINE, CNKI and the Cochrane Library databases up to MARCH 2015 were searched by use of several keywords in electronic databases. A meta-analysis was performed to clarify the impact of heparanase mRNA and protein on clinicopathological parameters in gastric cancer. Combined ORs with 95%CIs were calculated by Revman 5.0, and publication bias testing was performed by stata12.0. Results: A total of 27 studies which included 3,891 gastric cancer patients were combined in the final analysis. When stratifying the studies by the pathological variables of heparanase mRNA expression, the depth of invasion (633 patients) (OR=4.96; 95% CI=2.38-1.37; P<0.0001), lymph node metastasis (639 patients) (OR=6.22; 95%CI=2.70-14.34, P<0.0001), and lymph node metastasis (383 patients) (OR=6.85; 95% CI=2.04-23.04; P=0.002) were all significant. When stratifying the studies by the pathological variables of heparanase protein expression, this was the case for depth of invasion (1250 patients) (OR=2.76; 95% CI=1.52-5.03; P=0.0009), lymph node metastasis (1178 patients) (OR=4.79 ; 95% CI=3.37-6.80, P<0.00001), tumor size (727 patients) (OR=2.06 ; 95% CI=1.31-3.23; P=0.002) (OR=2.61; 95% CI=2.09-3.27; P=0.000), and TNM stage (1233 patients) (OR=6.85; 95% CI=2.04-23.04; P=0.002). Egger's tests suggested publication bias for depth of invasion, lymph node metastasis, lymph node metastasis and tumor size of heparanase mRNA and protein expression. Conclusions: This meta-analysis suggests that higher heparanase expression in gastric cancer is associated with clinicopathologic features of depth of invasion, lymph node metastasis and TNM stage at mRNA and protein levels, and of tumor size only at the protein level. Egger's tests suggested publication bias for these clinicopathologic features of heparanase mRNA and protein expression, and which may be caused by shortage of relevant studies. As a result, although abundant reports showed heparanase may be associated with clinicopathologic features in gastric cancer, this meta-analysis indicates that more strict studies were needed to evaluate its clinicopathologic significance.

• Asian Pacific Journal of Cancer Prevention
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• 제17권8호
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• pp.3785-3791
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• 2016

Background: Previous studies have assessed the association between the Cytotoxic T-lymphocyte Antigen-4(CTLA-4) polymorphism with the risk of malignant bone tumor, but the conclusions were inconsistent. We aimed to clarify association of cytotoxic T-lymphocyte antigen-4 polymorphisms with malignant bone tumors risk by performing a meta-analysis. Materials and Methods: The databases including PubMed, EMBase databases and the Cochrane Library were searched to identify the eligible studies prior to January 30 2016. Odds ratio (OR) with 95% confidence interval (95%CI) were used to estimate the strengths of the association between the CTLA-4 polymorphism and the malignant bone tumor risks. The meta-analysis was performed by STATA 12.0. Results: Four individual studies with a total of 1003 cases with malignant bone tumor and 1162 controls were included in our meta-analysis. The results of meta-analysis on those data demonstrated that CTLA-4 +49G>A polymorphism was associated with the risk of Ewing's sarcoma and osteosarcoma strongly (A vs. G: OR=1.36, 95%CI:1.20-1.54, p=0.000; AA+AG vs. GG: OR=1.35, 95%CI:1.14-1.61, p=0.001; AA vs. GG: OR=2.24, 95%CI:1.67-2.99, p=0.000; AA vs. AG+GG: OR=2.00, 95%CI:1.53-2.62, p=0.000), but CTLA-4 -318C/T polymorphism was not associated with the risk of malignant bone tumor (C vs. T: OR=0.76, 95%CI:0.76-1.08, p= 0.262; CC+CT vs. TT: OR=0.70, 95%CI:0.41-1.20, p= 0.198; CC vs. TT: OR=0.69, 95%CI:0.40-1.19, p= 0.183; CC vs. CT+TT: OR=0.92, 95%CI:0.75-1.13, p= 0.419). Subgroup analysis showed that there are significantly positive correlations between CTLA-4 +49G>A polymorphism and increased risks of malignant bone tumors in large size of sample (A vs. G: OR=1.347, 95%CI: 1.172,1.548, p=0.000; AA vs. GG: OR=2.228, 95%CI: 1.608,3.085, p=0.000), Ewing's Sarcoma or Osteosarcoma (A vs. G: OR=1.361, 95%CI: 1.201,1.540, p=0.000; AA vs. GG: OR=2.236, 95%CI: 1.674,2.986, p=0.000), and PCR-RFLP or Sequencing(A vs. G: OR=1.361, 95%CI: 1.201,1.540, p=0.000; AA vs. GG: OR=2.236, 95%CI: 1.674,2.986, p=0.000), but CTLA-4 -318C/T polymorphism was not associated with the risk of malignant bone tumors in diagnosis, genotype method, and sample size (all p>0.05). Conclusions: CTLA-4 +49A/G variant was associated with an increased risk of developing the malignant bone tumors, such as Ewing's sarcoma and osteosarcoma. However, it failed to show the association between CTLA-4 -318C/T polymorphism and the risk of malignant bone tumors. Future large-scale studies remain to be done to confirm our conclusions.

• Radiation Oncology Journal
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• 제17권2호
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• pp.151-157
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• 1999

목적 : HL60 세포주에서 PMA(phorbol 12-myrisate 13-acetate) 및 DMSO(dlmethyisulfoxlde) 에 의해 분화가 유도될 때 감소되는 특성을 보이는 K872 클론에 대한 염기 서열, 조직 분포, 단백 분리 등을 시행하였다. 재료 및 방법 QIA plasmid extraction kit(Qiagen GmbH, Germany)를 이용하여 사람의 모유두 세포 pBluescript phagemid cDNA library로부터 K872 클론을 추출하였다. Sanger's dideoxy nucleotide chain-termination method을 이용하여, 추출한 K872 클론의 염기 서열을 분석하였다. BLAST(Basic Local Alignment Search Tools) 프로그램으로 유전자은행의 염기 서열과의 상동성을 검색하였다. K872 클론으로 만든 probe로 다양한 인간 조직 및 암세포주로부터 분리한 RNA에 대하여 nothern blot을 시행하였다. His-Patch Thifusion expression system을 이용하여 대장균 배지에 0.1mM IPTG(Isopropyl-$\beta$-thlogalactopyranoslde) 를 첨가해서 결합단백의 유전자 발현을 유도하였다. 결합단백이 함유된 용출액을 SDS-PAGE에 걸어서 발현된 단백을 확인하였다. 결과 : K872 클론은 675개의 코딩 영역과 280개의 코딩과 관련없는 영역으로 구성된 1006개의 염기로 구성됨을 관찰하였다. 해독틀로 추정되는 부분은 시작 코돈을 포함하여 길6개의 아미노산을 형성하고 단백 산물의 분자량은 25,560 Da으로 추정되었다. 추정 아미노산 배열은 쥐의 glutathlone S-transferase kappa 1(rGSTKl) 의 아미노산 배열과 70$\%$의 상동성을 보였다. nothern blot에 따른 발현 양상은 심장, 수의근, 말초혈액 백혈구 등의 조직에서 높은 발현을 보였으며 방사선 내성과 관련지어 볼 때 대장암 및 흑색종 세포주에서 발현이 높았던 점은 특기할 만하였다. 결론 : 상동성 검색 결과 K872 유전자는 항암제 및 방사선 내성과 관련이 있는 rGSTK1에 대한 사람의 상동유전자로 사료되며 향후 이와 관련한 기능 분석이 필요할 것으로 사료된다

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제31권3호
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• pp.199-218
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• 2005

Purpose of Study: Peripheral nerve regeneration depends on neurotrophism of distal nerve stump, recovery potential of neuron, supporting cell like Schwann cell and neurotrophic factors such as BDNF. Peripheral nerve regeneration can be enhanced by the conduit which connects the both sides of transected nerve. The conduit maintains the effects of neurotrophism and BDNF produced by Schwann cells which can be made by gene therapy. In this study, we tried to enhance the peripheral nerve regeneration by using calcium phosphate coated porous conduit and BDNF-Adenovirus infected Schwann cells in sciatic nerve of rats. Materials and Methods: Microporous filter which permits the tissue fluid essential for nerve regeneration and does not permit infiltration of fibroblasts, was made into 2mm diameter and 17mm length conduit. Then it was coated with calcium phosphate to improve the Schwann cell adhesion and survival. The coated filter was evaluated by SEM examination and MTT assay. For effective allogenic Schwann cell culture, dorsal root ganglia of 1-day old rat were extracted and treated with enzyme and antimitotic Ara-C. Human BDNF cDNA was obtained from cDNA library and amplified using PCR. BDNF gene was inserted into adenovirus shuttle vector pAACCMVpARS in which E1 was deleted. We infected the BDNF-Ad into 293 human mammary kidney cell-line and obtained the virus plaque 2 days later. RT-PCR was performed to evaluate the secretion of BDNF in infected Schwann cells. To determine the most optimal m.o.i of BDNF-Ad, we infected the Schwann cells with LacZ adenovirus in 1, 20, 50, 75, 100, 250 m.o.i for 2 hours and stained with ${\beta}$-galactosidase. Rats(n=24) weighing around 300g were used. Total 14mm sciatic nerve defect was made and connected with calcium phosphate coated conduits. Schwann cells$(1{\times}10^6)$ or BDNF-Ad infected Schwann cells$(1{\times}10^6)$ were injected in conduit and only media(MEM) was injected in control group. Twelve weeks after surgery, degree of nerve regeneration was evaluated with gait analysis, electrophysiologic measurements and histomorphometric analysis. Results: 1. Microporous Millipore filter was effective conduit which permitted the adhesion of Schwann cells and inhibited the adhesion of fibroblast. We could enhance the Schwann cell adhesion and survival by coating Millipore filter with calcium phosphate. 2. Schwann cell culture technique using repeated treatment of Ara-C and GDNF was established. The mean number of Schwann cells obtained 1 and 2 weeks after the culture were $1.54{\pm}4.0{\times}10^6$ and $9.66{\pm}9.6{\times}10^6$. 3. The mRNA of BDNF in BDNF-Ad infected Schwann cells was detected using RT-PCR. In Schwann cell $0.69\;{\mu}g/{\mu}l$ of DNA was detected and in BDNF-Adenovirus transfected Schwann cell $0.795\;{\mu}g/{\mu}l$ of DNA was detected. The most effective infection concentration was determined by LacZ Adenovirus and 75 m.o.i was found the most optimal. Conclusion: BDNF-Ad transfected Schwann cells successfully regenerated the 14mm nerve gap which was connected with calcium phosphate coated Millipore filter. The BDNF-Ad group showed better results compared with Schwann cells only group and control group in aspect to sciatic function index, electrophysiologic measurements and histomorphometric analysis.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제28권5호
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• pp.375-395
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• 2006

Purpose: Lingual nerve (LN) damage may be caused by either tumor resection or injury such as wisdom tooth extraction, Although autologous nerve graft is sometimes used to repair the damaged nerve, it has the disadvantage of necessity of another operation for nerve harvesting. Moreover, the results of nerve grafting is not satisfactory. The nerve growth factor (NGF) is well-known to play a critical role in peripheral nerve regeneration and its local delivery to the injured nerve has been continuously tried to enhance nerve regeneration. However, its application has limitations like repeated administration due to short half life of 30 minutes and an in vivo delivery model must allow for direct and local delivery. The aim of this study was to construct a well-functioning $rhNGF-{\beta}$ adenovirus for the ultimate development of improved method to promote peripheral nerve regeneration with enhanced and extended secretion of hNGF from the injured nerve by injecting $rhNGF-{\beta}$ gene directly into crush-injured LN in rat model. Materials and Methods: $hNGF-{\beta}$ gene was prepared from fetal brain cDNA library and cloned into E1/E3 deleted adenoviral vector which contains green fluorescence protein (GFP) gene as a reporter. After large scale production and purification of $rhNGF-{\beta}$ adenovirus, transfection efficiency and its expression at various cells (primary cultured Schwann cells, HEK293 cells, Schwann cell lines, NIH3T3 and CRH cells) were evaluated by fluorescent microscopy, RT-PCR, ELISA, immunocytochemistry. Furthermore, the function of rhNGF-beta, which was secreted from various cells infected with $rhNGF-{\beta}$ adenovirus, was evaluated using neuritogenesis of PC-12 cells. For in vivo evaluation of efficacy of $rhNGF-{\beta}$ adenovirus, the LNs of 8-week old rats were exposed and crush-injured with a small hemostat for 10 seconds. After the injury, $rhNGF-{\beta}$ adenovirus($2{\mu}l,\;1.5{\times}10^{11}pfu$) or saline was administered into the crushed site in the experimental (n=24) and the control group (n=24), respectively. Sham operation of another group of rats (n=9) was performed without administration of either saline or adenovirus. The taste recovery and the change of fungiform papilla were studied at 1, 2, 3 and 4 weeks. Each of the 6 animals was tested with different solutions (0.1M NaCl, 0.1M sucrose, 0.01M QHCl, or 0.01M HCl) by two-bottle test paradigm and the number of papilla was counted using SEM picture of tongue dorsum. LN was explored at the same interval as taste study and evaluated electro-physiologically (peak voltage and nerve conduction velocity) and histomorphometrically (axon count, myelin thickness). Results: The recombinant adenovirus vector carrying $rhNGF-{\beta}$ was constructed and confirmed by restriction endonuclease analysis and DNA sequence analysis. GFP expression was observed in 90% of $rhNGF-{\beta}$ adenovirus infected cells compared with uninfected cells. Total mRNA isolated from $rhNGF-{\beta}$ adenovirus infected cells showed strong RT-PCR band, however uninfected or LacZ recombinant adenovirus infected cells did not. NGF quantification by ELISA showed a maximal release of $18865.4{\pm}310.9pg/ml$ NGF at the 4th day and stably continued till 14 days by $rhNGF-{\beta}$ adenovirus infected Schwann cells. PC-12 cells exposed to media with $rhNGF-{\beta}$ adenovirus infected Schwann cell revealed at the same level of neurite-extension as the commercial NGF did. $rhNGF-{\beta}$ adenovirus injected experimental groups in comparison to the control group exhibited different taste preference ratio. Salty, sweet and sour taste preference ratio were significantly different after 2 weeks from the beginning of the experiment, which were similar to the sham group, but not to the control group.

• 트랜스-
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• 제9권
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• pp.17-36
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• 2020

본 논문은 안산문화재단에서 운영하는 단원미술관의 전시 사례를 중심으로 콘텐츠 제작과 활용 그리고 확장 가능성에 대해 논의하는 데 그 목적을 가진다. 1991년 당시 문화체육관광부는 조선 후기 화원이자 풍속화의 대가로 알려진 단원 김홍도(檀園 金弘道, 1745~ ? )의 고향으로 추정되는 안산을 '단원의 도시'로 명명했다. 이에 안산은 단원 김홍도를 지역 고유의 자원으로 활용하고자 다각적인 노력을 기울이고 있다. 관광자원이자 문화콘텐츠로 단원 김홍도를 활용하여 단원조각공원 조성과 단원미술관 운영, 단원 김홍도 축제 기획 등 대내외적인 활동을 통해 단원 김홍도를 안산의 대표 브랜드화하고자 했다. 단원미술관은 단원 김홍도의 미술관이라고 지칭하기에 턱없이 부족한 수의 작품을 소장하고 있다. 2009년 <사슴과 동자>를 첫 매입하고 2016년 <화조도>를 매입한 이후 올해까지 단원 김홍도의 작품을 총 6점 소장하게 됐다.1 단원 김홍도의 작품을 수집하는데 현실적으로 많은 어려움이 따르기 때문이다. 이에 2015년 10월 개관한 단원콘텐츠관의 역할과 방향은 단원 김홍도의 진본을 소장하지 않아도 미술관의 역할과 기능이 가능하도록 하는 것이었다. 단원콘텐츠관을 단원 김홍도와 관련된 다양한 시각예술자료를 체계적으로 수집과 보존, 전시가 가능하도록 운영하고 디지털 자료 중심으로 고급 정보를 생산하여 이를 제공할 수 있도록 하는 비전을 설정했다. 다시 말해 도서관과 아카이브, 미술관(Library + Archive + Museum)의 기능이 결합된 One-Source Multi-Use의 복합문화 정보기관으로 단원콘텐츠관을 찾는 관람객의 욕구를 충족시킬 수 있도록 구축하고자 했다. 이는 소장품의 문제와 고서화(古書畫)가 가지는 전시의 한계를 극복하고 미술관의 역할과 기능을 충족시키는 등 동시대의 흐름을 반영하고 있어 여러 방면에서 시사하는 바가 크다. 단원 김홍도의 작품을 관람하고자 단원콘텐츠관을 찾는 관람객들에게 터치스크린과 딥 줌(Deep Zoom)의 기술을 이용하여 단원 김홍도의 디지털 아카이브를 실감형 서비스로 제공하고, 단원 김홍도의 원작을 그대로 해석하여 미디어 콘텐츠로 제작한 콘텐츠 전시를 통해 조선 시대 천재 화가 단원 김홍도의 작품세계를 쉽고 재미있게 접할 수 있도록 사업을 확장하고 있다.

• 한국전통조경학회지
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• 제39권4호
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• pp.24-37
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• 2021

본 연구는 대한제국과 그 전후의 시기를 중심으로 창덕궁 부용정과 주합루 권역의 원형 경관을 새롭게 조명하고, 향후 복원정비에 유용한 연구성과를 도출하기 위해 수행되었다. 연구 결과는 다음과 같이 요약할 수 있다. 첫째, 부용지 인공섬의 석축은 본래 정연하게 가공된 석재를 활용해 바른층쌓기로 조성되어 있었다. 하지만 1960~1970년대의 정비공사 과정에서 부용지 인공섬은 자연석과 가공석이 혼합된 형태로 변형되었다. 부용지 인공섬의 상부에 설치된 난간은 유사사례를 찾아보기 어려운 독특한 시설로 대한제국기에도 실존했지만, 일제강점기에 완전히 멸실되었다. 둘째, 오늘날 어수문 좌우에 남아 있는 취병은 2008년 조릿대를 기반으로 재현된 결과물이다. 어수문 취병의 식물 소재를 주목으로 보는 시각도 존재하지만, 구체적인 수종은 여전히 밝혀지지 않은 상태이다. 관련 자료와 정황을 다각적으로 고려하면 적어도 근대기의 어수문 취병은 동관왕묘와 경복궁 건청궁처럼 '향나무'로 제작되어 있었을 가능성이 높다. 셋째, 주합루 후원은 석계 형태의 구조물 위에 수목이 밀생하지 않은 공간이었다. 주합루 후원의 석계는 비교적 개방된 형태로 관리되면서 주변 건축물을 왕래할 수 있는 공간으로도 기능하였다. 하지만 1980년대 후반에 대규모 식재공사가 이루어지면서 주합루 후원은 화계와 같은 형태로 정비되었고, 다수의 화관목이 식재되어 폐쇄적인 공간으로 변모하였다. 넷째, 규장각과 개유와처럼 서고(書庫) 기능을 가졌던 영화당 남행각은 1900년대 후반 무렵에 멸실되어 본래 모습을 파악하기 어려운 건축물이었다. 본 연구에서는 근대기 사진과 스케치 자료를 토대로 영화당 남행각의 배치축을 확증하고, 형태와 의장적 특징을 확인하였다. 또한 기초자료 구축 차원에서 「동궐도」와 「동궐도형」을 참고한 추정복원도를 제시하였다.

• 지능정보연구
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• 제20권4호
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• pp.89-105
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• 2014

Web2.0의 등장과 함께 급속히 발전해온 온라인 포럼, 블로그, 트위터, 페이스북과 같은 소셜 미디어 서비스는 소비자와 소비자간의 의사소통을 넘어 이제 기업과 소비자 사이의 새로운 커뮤니케이션 매체로도 인식되고 있다. 때문에 기업뿐만 아니라 수많은 기관, 조직 등에서도 소셜미디어를 활용하여 소비자와 적극적인 의사소통을 전개하고 있으며, 나아가 소셜 미디어 콘텐츠에 담겨있는 소비자 고객들의 의견, 관심, 불만, 평판 등을 분석하고 이해하며 비즈니스에 적용하기 위해 이를 적극 분석하는 단계로 진화하고 있다. 이러한 연구의 한 분야로서 비정형 텍스트 콘텐츠와 같은 빅 데이터에서 저자의 감성이나 의견 등을 추출하는 오피니언 마이닝과 감성분석 기법이 소셜미디어 콘텐츠 분석에도 활발히 이용되고 있으며, 이미 여러 연구에서 이를 위한 방법론, 테크닉, 툴 등을 제시하고 있다. 그러나 아직 대량의 소셜미디어 데이터를 수집하여 언어처리를 거치고 의미를 해석하여 비즈니스 인사이트를 도출하는 전반의 과정을 제시한 연구가 많지 않으며, 그 결과를 의사결정자들이 쉽게 이해할 수 있는 시각화 기법으로 풀어내는 것 또한 드문 실정이다. 그러므로 본 연구에서는 소셜미디어 콘텐츠의 오피니언 마이닝을 위한 실무적인 분석방법을 제시하고 이를 통해 기업의사결정을 지원할 수 있는 시각화된 결과물을 제시하고자 하였다. 이를 위해 한국 인스턴트 식품 1위 기업의 대표 상품인 N-라면을 사례 연구의 대상으로 실제 블로그 데이터와 뉴스를 수집/분석하고 결과를 도출하였다. 또한 이런 과정에서 프리웨어 오픈 소스 R을 이용함으로써 비용부담 없이 어떤 조직에서도 적용할 수 있는 레퍼런스를 구현하였다. 그러므로 저자들은 본 연구의 분석방법과 결과물들이 식품산업뿐만 아니라 타 산업에서도 바로 적용 가능한 실용적 가이드와 참조자료가 될 것으로 기대한다.