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      Changes in SIRT gene expression during odontoblastic differentiation of human dental pulp cells

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      https://www.riss.kr/link?id=A103888583

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      Objectives: The aim of this study was to investigate the expression of 7 different sirtuin genes (SIRT1-SIRT7) in human dental pulp cells (HDPCs), and to determine the role of SIRTs in the odontoblastic differentiation potential of HDPCs. Materials and Methods: HDPCs were isolated from freshly extracted third molar teeth of healthy patients and cultulred in odontoblastic differentiation inducing media. Osteocalcin (OCN) and dentin sialophosphoprotein (DSPP) expression was analyzed to evaluate the odontoblastic differentiation of HDPCs by reverse transcription-polymerase chain reaction (RT-PCR), while alizarin red staining was used for the mineralization assay.
      To investigate the expression of SIRTs during odontoblastic differentiation of HDPCs, real time PCR was also performed with RT-PCR. Results: During the culture of HDPCs in the differentiation inducing media, OCN, and DSPP mRNA expressions were increased.
      Mineralized nodule formation was also increased in the 14 days culture. All seven SIRT genes were expressed during the odontogenic induction period. SIRT4 expression was increased in a time-dependent manner. Conclusions: Our study identified the expression of seven different SIRT genes in HDPCs, and revealed that SIRT4 could exert an influence on the odontoblast differentiation process. Further studies are needed to determine the effects of other SIRTs on the odontogenic potential of HDPCs.
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      Objectives: The aim of this study was to investigate the expression of 7 different sirtuin genes (SIRT1-SIRT7) in human dental pulp cells (HDPCs), and to determine the role of SIRTs in the odontoblastic differentiation potential of HDPCs. Materials an...

      Objectives: The aim of this study was to investigate the expression of 7 different sirtuin genes (SIRT1-SIRT7) in human dental pulp cells (HDPCs), and to determine the role of SIRTs in the odontoblastic differentiation potential of HDPCs. Materials and Methods: HDPCs were isolated from freshly extracted third molar teeth of healthy patients and cultulred in odontoblastic differentiation inducing media. Osteocalcin (OCN) and dentin sialophosphoprotein (DSPP) expression was analyzed to evaluate the odontoblastic differentiation of HDPCs by reverse transcription-polymerase chain reaction (RT-PCR), while alizarin red staining was used for the mineralization assay.
      To investigate the expression of SIRTs during odontoblastic differentiation of HDPCs, real time PCR was also performed with RT-PCR. Results: During the culture of HDPCs in the differentiation inducing media, OCN, and DSPP mRNA expressions were increased.
      Mineralized nodule formation was also increased in the 14 days culture. All seven SIRT genes were expressed during the odontogenic induction period. SIRT4 expression was increased in a time-dependent manner. Conclusions: Our study identified the expression of seven different SIRT genes in HDPCs, and revealed that SIRT4 could exert an influence on the odontoblast differentiation process. Further studies are needed to determine the effects of other SIRTs on the odontogenic potential of HDPCs.

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      참고문헌 (Reference)

      1 Imai S, "Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase" 403 : 795-800, 2000

      2 Lee YM, "The role of sirtuin 1 in osteoblastic differentiation in human periodontal ligament cells" 46 : 712-721, 2011

      3 Kim JJ, "The role of SIRT1 on angiogenic and odontogenic potential in human dental pulp cells" 38 : 899-906, 2012

      4 Sun HL, "The effect of SIRT6 on the odontoblastic potential of human dental pulp cells" 40 : 393-398, 2014

      5 Kitada M, "Sirtuins and renal diseases: relationship with aging and diabetic nephropathy" 124 : 153-164, 2013

      6 Verdin E, "Sirtuin regulation of mitochondria: energy production, apoptosis, and signaling" 35 : 669-675, 2010

      7 Morris BJ, "Seven sirtuins for seven deadly diseases of aging" 56 : 133-171, 2013

      8 Nasrin N, "SIRT4 regulates fatty acid oxidation and mitochondrial gene expression in liver and muscle cells" 285 : 31995-32002, 2010

      9 Li Z, "Regulation of SIRT2levels for human non-small cell lung cancer therapy" 82 : 9-15, 2013

      10 Fouad AF, "Pathways of the pulp" Mosby Elsevier 504-528, 2011

      1 Imai S, "Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase" 403 : 795-800, 2000

      2 Lee YM, "The role of sirtuin 1 in osteoblastic differentiation in human periodontal ligament cells" 46 : 712-721, 2011

      3 Kim JJ, "The role of SIRT1 on angiogenic and odontogenic potential in human dental pulp cells" 38 : 899-906, 2012

      4 Sun HL, "The effect of SIRT6 on the odontoblastic potential of human dental pulp cells" 40 : 393-398, 2014

      5 Kitada M, "Sirtuins and renal diseases: relationship with aging and diabetic nephropathy" 124 : 153-164, 2013

      6 Verdin E, "Sirtuin regulation of mitochondria: energy production, apoptosis, and signaling" 35 : 669-675, 2010

      7 Morris BJ, "Seven sirtuins for seven deadly diseases of aging" 56 : 133-171, 2013

      8 Nasrin N, "SIRT4 regulates fatty acid oxidation and mitochondrial gene expression in liver and muscle cells" 285 : 31995-32002, 2010

      9 Li Z, "Regulation of SIRT2levels for human non-small cell lung cancer therapy" 82 : 9-15, 2013

      10 Fouad AF, "Pathways of the pulp" Mosby Elsevier 504-528, 2011

      11 Haigis MC, "Mammalian sirtuins: biological insights and disease relevance" 5 : 253-295, 2010

      12 Wei X, "Expression of mineralization markers in dental pulp cells" 33 : 703-708, 2007

      13 Michishita E, "Evolutionarily conserved and nonconserved cellular localizations and functions of human SIRT proteins" 16 : 4623-4635, 2005

      14 Guarente L, "Calorie restriction and sirtuins revisited" 27 : 2072-2085, 2013

      15 Moschen AR, "Adipose tissue and liver expression of SIRT1, 3, and 6 increase after extensive weight loss in morbid obesity" 59 : 1315-1322, 2013

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2017-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2013-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2004-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2003-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      2000-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.25 0.25 0.21
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.21 0.19 0.448 0.1
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