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      Effects of three-dimensionally printed polycaprolactone/β-tricalcium phosphate scaffold on osteogenic differentiation of adipose tissue- and bone marrow-derived stem cells

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      https://www.riss.kr/link?id=A105908448

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      다국어 초록 (Multilingual Abstract)

      Background: Autogenous bone grafts have several limitations including donor-site problems and insufficient bone volume. To address these limitations, research on bone regeneration is being conducted actively. In this study, we investigate the effects of a three-dimensionally (3D) printed polycaprolactone (PCL)/tricalcium phosphate (TCP) scaffold on the osteogenic differentiation potential of adipose tissue-derived stem cells (ADSCs) and bone marrow-derived stem cells (BMSCs).
      Methods: We investigated the extent of osteogenic differentiation on the first and tenth day and fourth week after cell culture. Cytotoxicity of the 3D printed PCL/β-TCP scaffold was evaluated by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium assay, prior to osteogenic differentiation analysis. ADSCs and BMSCs were divided into three groups: C, only cultured cells; M, cells cultured in the 3D printed PCL/β-TCP scaffold; D, cells cultured in the 3D printed PCL/β-TCP scaffold with a bone differentiation medium. Alkaline phosphatase (ALP) activity assay, von Kossa staining, reverse transcription-polymerase chain reaction (RT-PCR), and Western blotting were performed for comparative analysis.
      Results: ALP assay and von Kossa staining revealed that group M had higher levels of osteogenic differentiation compared to group C. RT-PCR showed that gene expression was higher in group M than in group C, indicating that, compared to group C, osteogenic differentiation was more extensive in group M. Expression levels of proteins involved in ossification were higher in group M, as per the Western blotting results.
      Conclusion: Osteogenic differentiation was increased in mesenchymal stromal cells (MSCs) cultured in the 3D printed PCL/TCP scaffold compared to the control group. Osteogenic differentiation activity of MSCs cultured in the 3D printed PCL/TCP scaffold was lower than that of cells cultured on the scaffold in bone differentiation medium. Collectively, these results indicate that the 3D printed PCL/TCP scaffold promoted osteogenic differentiation of MSCs and may be widely used for bone tissue engineering.
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      Background: Autogenous bone grafts have several limitations including donor-site problems and insufficient bone volume. To address these limitations, research on bone regeneration is being conducted actively. In this study, we investigate the effects ...

      Background: Autogenous bone grafts have several limitations including donor-site problems and insufficient bone volume. To address these limitations, research on bone regeneration is being conducted actively. In this study, we investigate the effects of a three-dimensionally (3D) printed polycaprolactone (PCL)/tricalcium phosphate (TCP) scaffold on the osteogenic differentiation potential of adipose tissue-derived stem cells (ADSCs) and bone marrow-derived stem cells (BMSCs).
      Methods: We investigated the extent of osteogenic differentiation on the first and tenth day and fourth week after cell culture. Cytotoxicity of the 3D printed PCL/β-TCP scaffold was evaluated by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium assay, prior to osteogenic differentiation analysis. ADSCs and BMSCs were divided into three groups: C, only cultured cells; M, cells cultured in the 3D printed PCL/β-TCP scaffold; D, cells cultured in the 3D printed PCL/β-TCP scaffold with a bone differentiation medium. Alkaline phosphatase (ALP) activity assay, von Kossa staining, reverse transcription-polymerase chain reaction (RT-PCR), and Western blotting were performed for comparative analysis.
      Results: ALP assay and von Kossa staining revealed that group M had higher levels of osteogenic differentiation compared to group C. RT-PCR showed that gene expression was higher in group M than in group C, indicating that, compared to group C, osteogenic differentiation was more extensive in group M. Expression levels of proteins involved in ossification were higher in group M, as per the Western blotting results.
      Conclusion: Osteogenic differentiation was increased in mesenchymal stromal cells (MSCs) cultured in the 3D printed PCL/TCP scaffold compared to the control group. Osteogenic differentiation activity of MSCs cultured in the 3D printed PCL/TCP scaffold was lower than that of cells cultured on the scaffold in bone differentiation medium. Collectively, these results indicate that the 3D printed PCL/TCP scaffold promoted osteogenic differentiation of MSCs and may be widely used for bone tissue engineering.

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      참고문헌 (Reference)

      1 Carvalho PP, "Undifferentiated human adipose-derived stromal/stem cells loaded onto wet-spun starch-polycaprolactone scaffolds enhance bone regeneration: nude mice calvarial defect in vivo study" 102 : 3102-3111, 2014

      2 Yang S, "The design of scaffolds for use in tissue engineering. Part II: rapid prototyping techniques" 8 : 1-11, 2002

      3 Yang S, "The design of scaffolds for use in tissue engineering. Part I: traditional factors" 7 : 679-689, 2001

      4 Middleton JC, "Synthetic biodegradable polymers as orthopedic devices" 21 : 2335-2346, 2000

      5 Hutmacher DW, "Scaffold-based tissue engineering: rationale for computer-aided design and solid free-form fabrication systems" 22 : 354-362, 2004

      6 Minoda R, "Preliminary experience with beta-tricalcium phosphate for use in mastoid cavity obliteration after mastoidectomy" 28 : 1018-1021, 2007

      7 Xue R, "Polycaprolactone nanofiber scaffold enhances the osteogenic differentiation potency of various human tissue-derived mesenchymal stem cells" 8 : 148-, 2017

      8 Liao HT, "Osteogenesis of adipose-derived stem cells on polycaprolactone-$\beta$-tricalcium phosphate scaffold fabricated via selective laser sintering and surface coating with collagen type I" 10 : E337-E353, 2016

      9 Barry FP, "Mesenchymal stem cells: clinical applications and biological characterization" 36 : 568-584, 2004

      10 Choi D, "Mechano-chemical synthesis and characterization of nanostructured $\beta$-TCP powder" 27 : 377-381, 2007

      1 Carvalho PP, "Undifferentiated human adipose-derived stromal/stem cells loaded onto wet-spun starch-polycaprolactone scaffolds enhance bone regeneration: nude mice calvarial defect in vivo study" 102 : 3102-3111, 2014

      2 Yang S, "The design of scaffolds for use in tissue engineering. Part II: rapid prototyping techniques" 8 : 1-11, 2002

      3 Yang S, "The design of scaffolds for use in tissue engineering. Part I: traditional factors" 7 : 679-689, 2001

      4 Middleton JC, "Synthetic biodegradable polymers as orthopedic devices" 21 : 2335-2346, 2000

      5 Hutmacher DW, "Scaffold-based tissue engineering: rationale for computer-aided design and solid free-form fabrication systems" 22 : 354-362, 2004

      6 Minoda R, "Preliminary experience with beta-tricalcium phosphate for use in mastoid cavity obliteration after mastoidectomy" 28 : 1018-1021, 2007

      7 Xue R, "Polycaprolactone nanofiber scaffold enhances the osteogenic differentiation potency of various human tissue-derived mesenchymal stem cells" 8 : 148-, 2017

      8 Liao HT, "Osteogenesis of adipose-derived stem cells on polycaprolactone-$\beta$-tricalcium phosphate scaffold fabricated via selective laser sintering and surface coating with collagen type I" 10 : E337-E353, 2016

      9 Barry FP, "Mesenchymal stem cells: clinical applications and biological characterization" 36 : 568-584, 2004

      10 Choi D, "Mechano-chemical synthesis and characterization of nanostructured $\beta$-TCP powder" 27 : 377-381, 2007

      11 Sachlos E, "Making tissue engineering scaffolds work. Review: the application of solid freeform fabrication technology to the production of tissue engineering scaffolds" 5 : 29-39, 2003

      12 Rose FR, "In vitro assessment of cell penetration into porous hydroxyapatite scaffolds with a central aligned channel" 25 : 5507-5514, 2004

      13 Guan J, "Human urine derived stem cells in combination with $\beta$-TCP can be applied for bone regeneration" 10 : e0125253-, 2015

      14 김선종, "Effects of Polycaprolactone-Tricalcium Phosphate, Recombinant Human Bone Morphogenetic Protein-2 and Dog Mesenchymal Stem Cells on Bone Formation: Pilot Study in Dogs" 연세대학교의과대학 50 (50): 825-831, 2009

      15 Matsuno T, "Development of beta-tricalcium phosphate/collagen sponge composite for bone regeneration" 25 : 138-144, 2006

      16 Arafat MT, "Biomimetic composite coating on rapid prototyped scaffolds for bone tissue engineering" 7 : 809-820, 2011

      17 Burg KJ, "Biomaterial developments for bone tissue engineering" 21 : 2347-2359, 2000

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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
      2017-01-01 평가 등재후보학술지 유지 (계속평가) KCI등재후보
      2016-01-01 평가 등재후보학술지 유지 (계속평가) KCI등재후보
      2014-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2013-12-01 평가 등재후보 탈락 (등재후보2차)
      2012-04-10 학술지명변경 한글명 : 대한두개안면성형외과학회지 -> Archives of Craniofacial Surgery
      외국어명 : Journal of the korean cleft palate-craniofacial association -> Archives of Craniofacial Surgery
      KCI등재후보
      2012-01-01 평가 등재후보 1차 FAIL (기타) KCI등재후보
      2010-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
      2008-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2006-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.1 0.08 0.15
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.11 0.398 0
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