• 대한치과교정학회지
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• 제40권5호
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• pp.325-333
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• 2010

발음장애, 구토감 및 착용 불편감과 같은 보정장치에 대해 환자가 느끼는 불편감을 평가해보기 위해 고정식 교정장치로 교정치료를 받고 교정장치가 제거된 66명(남자 23명, 여자 43명; 평균연령 $23.42{\pm}10.19$)의 교정환자를 대상으로 무작위로 두 군으로 배정한 후 고정식 교정장치를 제거한 다음 날 CWR 장착군에게는 구개를 완전히 덮는 구개 완전 피개형 보정장치인 conventional wraparound retainer (CWR)를 장착시키고 CCR 장착군에게는 구개를 말 발굽 모양으로 부분 피개하는 보정장치인 circumferential comfortable retainer (CCR)를 4주 동안 장착시킨 후 발음장애, 구토감 및 착용 불편감의 정도에 대해 100-mm visual analog scale (VAS)로 표시할 수 있도록 제작된 설문지를 통해 얻은 점수에 대해 통계적으로 비교 분석하였다. 연구결과 발음장애와 착용 불편감의 비교에서 CCR 장착군이 CWR 장착군에 비해 통계적으로 유의하게 낮았다 ($p$ < 0.05). 구토감의 비교에서는 CCR 장착군이 CWR 장착군에 비해 낮은 점수를 보였지만 통계적으로는 유의한 차이를 보이지 않았다 ($p$ = 0.146). 이상의 연구 결과로 circumferential comfortable retainer (CCR)는 발음장애를 감소시키고, 착용 불편감을 완화시킴으로써 환자의 협조도를 증진시켜줄 수 있는바 고정식 교정장치를 이용한 교정치료 후 치료결과 유지에 도움이 될 수 있음을 시사하였다.

• 생명과학회지
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• 제13권4호
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• pp.541-550
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• 2003

본 실험에서는 C형 간염바이러스 (HCV)의 외피 단백질인 E2 당단백질에 결합하는 세포단백질들을 클로닝하기 위해 간세포 cDNA를 phage 표면에 발현시킨 phage library를 제작하였고, 12-mer peptide library와 함께 E2 단백질에 대해 panning을 실시하였다. 검색결과 세포내 신호전달과 cytoskeleton 구성에 관여하는 tensin, membrane protein band 4.1 등 세포질내 단백질과 CCR7, CKR-L2, insulin-like growth factor-1 receptor 등 세포막 단백질 등이 확인되었다. 이들 단백질들을 발현하는 phage들은 수용성 E2단백질을 이용한 결합중화반응 결과 E2 단백질에 특이적으로 결합함이 확인되었다. 사람 T 세포에서 주로 발현되는 CCR7 유전자를 PHA로 활성화된 사람 T 세포의 total RNA를 이용하여 증폭하고 클로닝하였다. 293T 세포에 transfection시켜 단백질 발현양상을 flow cytometer로 분석하여 70% 이상의 세포들이 CCR7을 발현하고 있음을 관찰하였다. 수용성 E2 단백질을 CCR7이 transfection된 세포와 mock transfection된 대조군 세포에 각각 반응시킨 결과 dose-dependent 양상으로 CCR7에 결합하였다.

• 통합자연과학논문집
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• 제7권4호
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• pp.234-240
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• 2014

C-C chemokine receptor type 4 (CCR4) is a chemokine receptor with seven transmembrane helices and it belongs to the GPCR family. It plays an important role in asthma, lung disease, atopic dermatitis, allergic bronchopulmonary aspergillosis, cancer, inflammatory bowel disease, the mosquito-borne tropical diseases, such as dengue fever and allergic rhinitis. Because of its role in wide spectrum of disease processes, CCR4 is considered to be an important drug target. Three dimensional structure of the protein is essential to determine the functions. In the present study homology modeling of human CCR4 was performed based on crystal structure of CCR5 chemokine receptor. The generated models were validated using various parameters. Among the generated homology models the best one is selected based on validation result. The model can be used for performing further docking studies to identifying the critical interacting residues.

• 한국콘텐츠학회논문지
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• 제10권11호
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• pp.371-379
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• 2010

본 연구는 자료포락분석(DEA)을 이용하여 가장 최근의 객관적 자료인 대학행정정보 공시자료를 입수하여 충청지역 대학의 상대적 효율성을 분석하였다. 본 연구결과는 다음과 같다. 첫째, CCR 효율성이 1인 사립대학교는 15개 대학교 가운데 5개 대학교인데, 충남지역에 3개 대학교, 충북지역의 2개 대학교로 나타났으며, 충북지역에 위치한 대학교들의 CCR 효율성 값 평균이 충남과 대전지역 사립대학교들의 CCR 효율성 값 평균보다 큰 것으로 나타났다. 둘째, 충청지역 2년제 사립대학의 경우 CCR 효율성이 1인 사립대학은 13개 대학 가운데 3개 대학교인데, 대전지역에 2개 대학, 충북지역의 1개 대학으로 나타났으며, 대전지역에 위치한 대학들의 CCR 효율성 값 평균이 충남과 충북지역 사립대학들의 CCR 효율성 값 평균보다 큰 것으로 나타났다. 셋째, BCC 효율성이 1인 사립대학교는 15개 대학교 가운데 9개 대학교인데, 충남지역에 6개 대학교, 충북지역의 3개 대학교로 나타났으며, 충북지역에 위치한 대학교들의 BCC 효율성 값 평균이 충남과 대전지역 사립대학교들의 BCC 효율성 값 평균보다 큰 것으로 나타났다. 넷째, BCC 효율성이 1인 사립 대학은 13개 대학 가운데 7개 대학인데, 대전지역에 3개 대학, 충남지역의 2개 대학, 충북의 경우 효율성이 1인 대학은 2개 대학으로 나타났으며, 충북지역에 위치한 대학들의 BCC 효율성 값 평균이 대전과 충남지역 사립대학들의 BCC 효율성 값 평균보다 큰 것으로 나타났다.

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3429-3443
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• 2013

Chemokine receptor (CCR2) is a G protein-coupled receptor that contains seven transmembrane helices. Recent pharmaceutical research has focused on the antagonism of CCR2 and candidate drugs are currently undergoing clinical studies for the treatment of diseases like arthritis, multiple sclerosis, and type 2 diabetes. In this study, we analyzed the time dependent behavior of CCR2 docked with a potent 4-azetidinyl-1-aryl-cyclohexane (4AAC) derivative using molecular dynamics simulations (MDS) for 20 nanoseconds (ns). Homology modeling of CCR2 was performed and the 4AAC derivative was docked into this binding site. The docked model of selected conformations was then utilized to study the dynamic behavior of the 4AAC enzyme complexes inside lipid membrane. MDS of CCR2-16b of 4AAC complexes allowed us to refine the system since binding of an inhibitor to a receptor is a dynamic process and identify stable structures and better binding modes. Structure activity relationships (SAR) for 4AAC derivatives were investigated and reasons for the activities were determined. Probable binding pose for some CCR2 antagonists were determined from the perspectives of binding site. Initial modeling showed that Tyr49, Trp98, Ser101, Glu291, and additional residues are crucial for 4AAC binding, but MDS analysis showed that Ser101 may not be vital. 4AAC moved away from Ser101 and the hydrogen bonding between 4AAC and Ser101 vanished. The results of this study provide useful information regarding the structure-based drug design of CCR2 antagonists and additionally suggest key residues for further study by mutagenesis.

• IMMUNE NETWORK
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• 제20권6호
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• pp.49.1-49.15
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• 2020

C-C chemokine receptor type 5 (CCR5) regulates the trafficking of various immune cells to sites of infection. In this study, we showed that expression of CCR5 and its ligands was rapidly increased in the kidney after systemic Candida albicans infection, and infected CCR5^-/- mice exhibited increased mortality and morbidity, indicating that CCR5 contributes to an effective defense mechanism against systemic C. albicans infection. The susceptibility of CCR5^-/- mice to C. albicans infection was due to impaired fungal clearance, which in turn resulted in exacerbated renal inflammation and damage. CCR5-mediated recruitment of NK cells to the kidney in response to C. albicans infection was necessary for the anti-microbial activity of neutrophils, the main fungicidal effector cells. Mechanistically, C. albicans induced expression of IL-23 by CD11c⁺ dendritic cells (DCs). IL-23 in turn augmented the fungicidal activity of neutrophils through GM-CSF production by NK cells. As GM-CSF potentiated production of IL-23 in response to C. albicans, a positive feedback loop formed between NK cells and DCs seemed to function as an amplification point for host defense. Taken together, our results suggest that CCR5-mediated recruitment of NK cells to the site of fungal infection is an important step that underlies innate resistance to systemic C. albicans infection.

• IMMUNE NETWORK
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• 제3권1호
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• pp.29-37
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• 2003

Background: CC chemokine receptor (CCR) 7 and cognate CCR7 ligands, CCL21 (formerly secondary lymphoid tissue chemokine [SLC]) and CCL19 (formerly Epstein-Barr virus-induced molecule 1 ligand chemokine [ELC]), were known to establish microenvironment for the initiation of immune responses in secondary lymphoid tissue. As described previously, coadministration of DNA vaccine with CCR7 ligand-encoding plasmid DNA elicited enhanced humoral and cellular immunity via increasing the number of dendritic cells (DC) in secondary lymphoid tissue. The author hypothesized here that CCR7 ligand DNA could effectively expand memory CD4+ T cells to protect from viral infection likely via increasing DC number. Methods: To evaluate the effect of CCR7 ligand DNA on the expansion of memory CD4+ T cells, DO11.10.BALB/c transgenic (Tg)-mice, which have highly frequent ovalbumin $(OVA)_{323-339}$ peptide-specific CD4+ T cells, were used. Tg-mice were previously injected with CCR7 ligand DNA, then immunized with $OVA_{323-339}$ peptide plus complete Freund's adjuvant. Subsequently, memory CD4+ T cells in peripheral blood lymphocytes (PBL) were analyzed by FACS analysis for memory phenotype ($CD44^{high}$ and CD62 $L^{low}$) at memory stage. Memory CD4+ T cells recruited into inflammatory site induced with OVA-expressing virus were also analyzed. Finally, the protective efficacy against viral infection was evaluated. Results: CCR7 ligand DNA-treated Tg-mice showed more expanded $CD44^{high}$ memory CD4+ T cells in PBL than control vector-treated animals. The increased number of memory CD4+ T cells recruited into inflammatory site was also observed in CCR7 ligand DNA-treated Tg-mice. Such effectively expanded memory CD4+ T cell population increased the protective immunity against virulent viral infection. Conclusion: These results document that CCR7 and its cognate ligands play an important role in intracellular infection through establishing optimal memory T cell. Moreover, CCR7 ligand could be useful as modulator in DNA vaccination against viral infection as well as cancer.

• International Journal of Oral Biology
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• 제44권4호
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• pp.173-181
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• 2019

The CC chemokine receptor 5 (CCR5) is a G protein-coupled receptor that regulates chemotaxis and effector functions of immune cells. It also serves as the major co-receptor for the entry of human immunodeficiency virus (HIV). Recently, CCR5 inhibitors have been developed and used for the treatment or prevention of HIV infections. Additionally, it has been identified that CCR5 controls bone homeostasis by regulating osteoclastogenesis and the communication between osteoblasts and osteoclasts. However, the effects of CCR5 inhibition on bone tissue in elderly patients are unknown. This study aimed to examine the bone phenotype of aged CCR5 knockout (KO) mice. Femoral and tibial bones were isolated from 12-month and 18-month old wild-type (WT) and CCR5 KO mice, and microcomputed tomography and histology analyses were performed. Twelve-month-old CCR5 KO mice exhibited a decreased trabecular bone mass and cortical bone thickness in both femoral and tibial bones compared with age-matched WT mice. Eighteen-month-old mice also showed a decreased trabecular bone mass in femurs compared with control WT mice, but not in tibial bones. Unlike in 12-month-old mice, the cortical margin of femurs and tibias in 18-month-old mice were rough, likely because they were aggravated by the deficiency of CCR5. Overall, our data suggest that the deficiency of CCR5 with aging can cause severe bone loss. When CCR5 inhibitors or CCR5 inactivating technologies are used in elderly patients, a preventive strategy for bone loss should be considered.

• Journal of Plant Biotechnology
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• 제38권4호
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• pp.278-284
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• 2011

The CCR4-CAF1-NOT complex-mediated degradation of mRNA is a fundamental aspect of gene regulation in eukaryotes. We herein examined the role of AtCAF1 in the innate immune and wound responses of plants. Our results showed that overexpression of AtCAF1 significantly downregulated the transcript level of EFR but not FLS2 and BRI1, as well as abolished up-regulated expression pattern of EFR in response to wounding. Consistently, Agrobacteriummediated transient expression of GUS was highly enhanced in the transgenic plants overexpressing AtCAF. Furthermore, JA responsive genes were down-regulated by overexpression of AtCAF, causing the transgenic plants overexpressing AtCAF more susceptible to necrotrophic fungal pathogen, Botrytis cinerea. These results suggest that The CCR4-CAF1-NOT complex-mediated degradation of mRNA negatively regulates wounding-mediated disease resistance in Arabidopsis thaliana.

• 한국문헌정보학회지
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• 제47권3호
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• pp.275-293
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• 2013

이 연구는 고전자료 이용에 필요한 목록기술규칙의 이해와 동양 고전자료 목록(서지기술) 네트워크를 위하여 한국목록규칙 4판(KCR 4)과 중국문헌편목규칙 2판(CCR 2)에서의 고전자료의 목록기술 규칙을 다음과 같이 비교 분석하였다. 첫째, 기술총칙의 비교를 위하여 기술의 대상과 기술사항의 구성, 기재순위와 구두점 그리고 기술의 정보원을 대상으로 진행하였다. 그 결과 KCR 4는 책임표시와 판사항의 정보원 규정이 상세하며, CCR 2는 출판 발행사항 및 총서사항의 정보원 규정이 상세하였다. 둘째, 세부사항의 비교를 위하여 표제와 책임표시사항, 판사항, 발행사항 및 형태사항 그리고 주기사항을 대상으로 진행하였다. 그 결과 판종의 기술과 발행사항의 경우 KCR 4가 상세하게 규정하고 있으며, 주기사항의 경우 CCR 2의 제요가 특징적이었다.