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      Protein transduction domain을 이용한 recombinant human bone morphogenetic protein-2의 골재생효과 = Bone regenerative effects of recombinant human bone morphogenetic protein-2 employed protein transduction domain

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      https://www.riss.kr/link?id=A101528271

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      다국어 초록 (Multilingual Abstract)

      Bone morphogenetic proteins(BMPs) are regarded as members of the transforming growth $factor-{\beta}$ superfamily with characteristic features in their amino acid sequences. A number of studies have demonstrated the biologic activities of BMPs, which ...

      Bone morphogenetic proteins(BMPs) are regarded as members of the transforming growth $factor-{\beta}$ superfamily with characteristic features in their amino acid sequences. A number of studies have demonstrated the biologic activities of BMPs, which include the induction of cartilage and bone formation. Recently there was a attempt to overcome a limitation of mass production, and economical efficieny of rh-BMPs. The method producing PTD by using bacteria have advantages of acquiry a mass of proteins. Hences, a new treatment which deliver protein employed by protein transduction domain(PTD) has been tried. The purpose of this study was to evaluate the bone regenerative effect of TATBMP-2 and TAT-HA2-BMP-2 employed by PTD from HlV-1 TAT protein for protein translocation in the rat calvarial model. An 8mm calvarial, critical size osteotomy defect was created in each of 32 male Spraque-Dawley rats(weight $250{\sim}300g$). The animals were divided into 4 groups of 32 animals each (4 animals/group/healing interval). The defect was treated with TATBMP-2/ACS(Absorbable collagen sponge) (TATBMP-2 0.1mg/ml), TAT-HA2-BMP-2/ACS(TAT-HA2-BMP-2 0.1mg/ml), ACS alone or left untreated for surgical control(negative control). The rats were sacrificed at 2 or 8 weeks postsurgery, and the results were evaluated histologically. The results were as follows: New bone formation were not significantly greater in the TATBMP-2/ACS group relative to negative, and positive control groups. New bone was evident at the defect sites in TAT-HA2-BMP-2/ACS group relative to negative, positive control and TATBMP-2 groups. There were a little bone regeneration in TATBMP-2 groups. While, enhanced local bone formation were observed in TAT-HA2-BMP-2 group. But, The results was not the same in all rat defects. Therefore, further investigations are required to develop a method. which disperse homogenously, and adhere to target cells.

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      참고문헌 (Reference)

      1 Recombinant human osteogenic protein-1, "induces new bone formation in vivo with a specific activity comparable with natural bovine osteogenic protein and stimulates osteoblast proliferation and differentiation in vitro" 20352-1 20362,

      2 Tseng YL, "Translocation of liposomes into cancer cells by cell-penetrating peptides penetratin and tat: a kinetic and efficacy study" 62 : 864-872, 2002

      3 Wadia JS, "Transducible TAT-HA fusogenic peptide enhances escape of TAT-fusion proteins after lipid raft macropinocytosis" 10 : 310-315, 2004

      4 Griffith DL, "Three-dimensional structure of recombinant human osteogenic protein 1: structural paradigm for the transforming growth factor beta superfamily" 93 : 878-883, 1996

      5 Joliot AH, "The third helix of the Antennapedia homeodomain translocates through biological membranes" 10444-10450,

      6 Takagi K, "The reaction of the dura to bone morphogenetic protein in repair of skull defects" 100-109,

      7 Baum BJ, "The impact of gene therapy on dentistry: a revisiting after six years" 133 : 35-44, 2002

      8 Cook SD, "The effect of recombinant human osteogenic protein-1 on healing of large segmental bone defects" 827-838,

      9 Hong SJ, "The effect of a fibrin-fibronectin/beta-tricalcium phosphate/recombinant human bone morphogenetic protein-2 system on bone formation in rat calvarial defects" 27 : 3810-3816, 2006

      10 Schmitz JP, "The critical size defect as an experimental model for craniomandibulofacial nonunions" 299-308,

      1 Recombinant human osteogenic protein-1, "induces new bone formation in vivo with a specific activity comparable with natural bovine osteogenic protein and stimulates osteoblast proliferation and differentiation in vitro" 20352-1 20362,

      2 Tseng YL, "Translocation of liposomes into cancer cells by cell-penetrating peptides penetratin and tat: a kinetic and efficacy study" 62 : 864-872, 2002

      3 Wadia JS, "Transducible TAT-HA fusogenic peptide enhances escape of TAT-fusion proteins after lipid raft macropinocytosis" 10 : 310-315, 2004

      4 Griffith DL, "Three-dimensional structure of recombinant human osteogenic protein 1: structural paradigm for the transforming growth factor beta superfamily" 93 : 878-883, 1996

      5 Joliot AH, "The third helix of the Antennapedia homeodomain translocates through biological membranes" 10444-10450,

      6 Takagi K, "The reaction of the dura to bone morphogenetic protein in repair of skull defects" 100-109,

      7 Baum BJ, "The impact of gene therapy on dentistry: a revisiting after six years" 133 : 35-44, 2002

      8 Cook SD, "The effect of recombinant human osteogenic protein-1 on healing of large segmental bone defects" 827-838,

      9 Hong SJ, "The effect of a fibrin-fibronectin/beta-tricalcium phosphate/recombinant human bone morphogenetic protein-2 system on bone formation in rat calvarial defects" 27 : 3810-3816, 2006

      10 Schmitz JP, "The critical size defect as an experimental model for craniomandibulofacial nonunions" 299-308,

      11 Michiue H, "The NH2 terminus of influenza virus hemagglutinin-2 subunit peptides enhances the antitumor potency of polyarginine-mediated p53 protein transduction" 280 : 8285-8289, 2005

      12 Fawell S, "Tat-mediated delivery of heterologous proteins into cells" 664-668,

      13 Lewin M, "Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells" 18 : 410-414, 2000

      14 Gitelman SE, "Recombinant Vgr-1/BMP-6-expressing tumors induce fibrosis and endochondral bone formation in vivo" 1595-1609,

      15 Schwarze SR, "Protein transduction: unrestricted delivery into all cells?" 10 : 290-295, 2000

      16 Wikesjo UM, "Periodontal repair in dogs: effect of rhBMP-2 concentration on regeneration of alveolar bone and periodontal attachment" 26 : 392-400, 1999

      17 Wozney JM, "Novel regulators of bone formation" 1528-1534, science1988;242

      18 Park J, "Mutational analysis of a human immunodeficiency virus type 1 Tat protein transduction domain which is required for delivery of an exogenous protein into mammalian cells" 83 : 1173-1181, 2002

      19 Schwarze SR, "In vivo protein transduction: intracellular delivery of biologically active proteins, compounds and DNA" 21 : 45-48, 2000

      20 Celeste AJ, "Identification of transforming growth factor beta family members present in bone-inductive protein purified from bovine bone" 9843-9847,

      21 Baltzer AW, "Genetic enhancement of fracture repair healing of an experimental segmental defect by adenoviral transfer of the BMP-2 gene" 7 : 734-739, 2000

      22 Winn SR, "Gene therapy approaches for modulating bone regeneration" 42 : 121-138, 2000

      23 Amano M, "Formation of actin stress fibers and focal adhesions enhanced by Rho-kinase" 275 : 1308-1311, 1997

      24 King GN, "Factors that modulate the effects of bone morphogenetic protein-induced periodontal regeneration: a critical review" 73 : 925-936, 2002

      25 Ahn SH, "Effect of recombinant human bone morphogenetic protein-4 with carriers in rat calvarial defects" 74 : 787-797, 2003

      26 Pang EK, "Effect of recombinant human bone morphogenetic protein-4 dose on bone formation in a rat calvarial defect model" 75 : 1364-1370, 2004

      27 Choi SH, "Effect of recombinant human bone morphogenetic protein-2/absorbable collagen sponge (rhBMP-2/ACS) on healing in 3-wall intrabony defects in dogs" 73 : 63-72, 2002

      28 Hyun SJ, "Effect of recombinant human bone morphogenetic protein-2, -4, and -7 on bone formation in rat calvarial defects" 76 : 1667-1674, 2005

      29 Han DK, "Effect of a fibrin-fibronectin sealing system as a carrier for recombinant human bone morphogenetic protein-4 on bone formation in rat calvarial defects" 76 : 2216-2222, 2005

      30 Frankel AD, "Cellular uptake of the tat protein from human immunodeficiency virus" 1189-1193,

      31 Fittipaldi A, "Cell membrane lipid rafts mediate caveolar endocytosis of HIV-1 Tat fusion proteins" 278 : 34141-34149, 2003

      32 Urist MR, "Bone: formation by autoinduc- tion. 1965" 4-10, 2002

      33 Reddi AH, "Bone morphogenetic proteins: from basic science to clinical applications" 83 (83): S1-S6, 2001

      34 Groeneveld EH, "Bone morphogenetic proteins in human bone regenera- tion" 142 : 9-21, 2000

      35 Chen D, "Bone morphogenetic proteins" 22 : 233-241, 2004

      36 Cook SD, "Bone defect healing with an osteogenic protein-1 device combined with carboxymethylcellulose" 75 : 137-145, 2005

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2012-03-21 학술지명변경 한글명 : The Journal of the Korean Academy of Periodontology (JPIS) -> Journal of Periodontal & Implant Science
      외국어명 : THE JOURNAL OF KOREAN ACADEMY OF PERIODONTOLOGY -> Journal of Periodontal & Implant Science
      KCI등재
      2011-03-22 학술지명변경 한글명 : 대한치주과학회지 -> The Journal of the Korean Academy of Periodontology (JPIS) 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
      2002-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.91 0.14 0.66
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.56 0.45 0.49 0.02
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