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아라키돈산 유도 염증모델에서 LED 광조사에 의한 유전자 발현에 관한 KCI 등재

Gene Expression Profiling of Archidonic Acid-Treated Inflammatory Model in Human Gingival Fibroblast

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  • URLhttps://db.koreascholar.com/Article/Detail/292857
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대한구강악안면병리학회지 (The Korean Journal of Oral and Maxillofacial Pathology)
대한구강악안면병리학회 (Korean Academy Of Oral And Maxillofacial Pathology)
초록

To investigate the differential expression of genes by 635nm LEDs irradiation in arachidonic acid-treated human gingival fibroblasts, cDNA microarray was carried out. Human gingival fibroblasts were primary cultured and arachidonic acid was treated to induce inflammation. 635nm of wave length was used for LEDs irradiation. The experimental group was categorized into four group ; control, only LEDs irradiation group, only arachidonic acid-treated group and arachidonic acid-treated with LEDs irradiation group. The expression of 8,078 genes were increased and the expression of 7,103 genes were decreased in only LEDs irradiation group. For arachidonic acid-treated with LEDs irradiation group, the expression of 6,815 genes were increased, while the expression of 8,031 genes were decreased comparing with only arachidonic acid-treated group. IL-13alpha2 receptor was the most expressed gene in LEDs irradiation group comparing with control, followed by MMP3. Genes which the most down regulated was BIRC3 in LEDs irradiation group. PLAB genes was the most up-regulated in arachidonic acid treated with LEDs irradation group, followed by ranked RARRES1. Considering the classification by cell function, genes associated with signal transduction were the most affected by LEDs irradiation, followed by the genes associated with nucleoside, nucleotide and nucleic acid metabolism. In arachidonic acid treated with LEDs irradiation, genes associated with signal transduction and protein metabolism were affected. Taken together, LEDs irradiation could affect various biological process and could identify many genes related to LEDs irradiation, which could be used for clinical application.

목차
I. 서론
 II. 재료 및 방법
  1. 치은섬유아세포의 배양 및 시료 처리
  2. LED 광 조사
  3. RNA 추출
  4. Illumina microarray 분석
  5. 스캔 및 결과(데이터) 분석
  6. 통계 처리(Statistical Data Analysis)
 III. 결과
  1. Sample Quality Check
  2. Microarray 분석 결과
 IV. 고찰
 V. 결론
 VI. 참고문헌
저자
  • 김한일(전남대학교 치의학전문대학원 보존학교실, 전남대학교 치의학전문대학원 구강내과학교실) | Han Il Kim
  • 김인애(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | In Ae Kim
  • 정민아(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | Min A Chung
  • 임원봉(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | Won Bong Lim
  • 이성가(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | Sung Ga Lee
  • 김병국(전남대학교 치의학전문대학원 구강내과학교실) | Byung Gook Kim
  • 황윤찬(전남대학교 치의학전문대학원 보존학교실) | Yun Chan Hwang
  • 황인남(전남대학교 치의학전문대학원 보존학교실) | In Nam Hwang
  • 오원만(전남대학교 치의학전문대학원 보존학교실) | Won Mann Oh
  • 최홍란(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | Hong Ran Choi correspondence
  • 김옥준(전남대학교 치의학전문대학원 구강병리학교실 및 치의학연구소) | Ok Joon Kim