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      KCI등재 SCIE SCOPUS

      Electrospun Microvasculature for Rapid Vascular Network Restoration

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      https://www.riss.kr/link?id=A107268128

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      다국어 초록 (Multilingual Abstract)

      Background: Sufficient blood supply through neo-vasculature is a major challenge in cell therapy and tissue engineering in order to support the growth, function, and viability of implanted cells. However, depending on the implant size and cell types, ...

      Background: Sufficient blood supply through neo-vasculature is a major challenge in cell therapy and tissue engineering in order to support the growth, function, and viability of implanted cells. However, depending on the implant size and cell types, the natural process of angiogenesis may not provide enough blood supply for long term survival of the implants, requiring supplementary strategy to prevent local ischemia. Many researchers have reported the methodologies to form pre-vasculatures that mimic in vivo microvessels for implantation to promote angiogenesis. These approaches successfully showed significant enhancement in long-term survival and regenerative functions of implanted cells, yet there remains room for improvement.




      Methods: This paper suggests a proof-of-concept strategy to utilize novel scaffolds of dimpled/hollow electrospun fibers that enable the formation of highly mature pre-vasculatures with adequate dimensions and fast degrading in the tissue.




      Result: Higher surface roughness improved the maturity of endothelial cells mediated by increased cell-scaffold affinity. The degradation of scaffold material for functional restoration of the neo-vasculatures was also expedited by employing the hollow scaffold design based on co-axial electrospinning techniques.




      Conclusion: This unique scaffold-based pre-vasculature can hold implanted cells and tissue constructs for a prolonged time while minimizing the cellular loss, manifesting as a gold standard design for transplantable scaffolds.

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      다국어 초록 (Multilingual Abstract)

      Background: Sufficient blood supply through neo-vasculature is a major challenge in cell therapy and tissue engineering in order to support the growth, function, and viability of implanted cells. However, depending on the implant size and cell types, ...

      Background: Sufficient blood supply through neo-vasculature is a major challenge in cell therapy and tissue engineering in order to support the growth, function, and viability of implanted cells. However, depending on the implant size and cell types, the natural process of angiogenesis may not provide enough blood supply for long term survival of the implants, requiring supplementary strategy to prevent local ischemia. Many researchers have reported the methodologies to form pre-vasculatures that mimic in vivo microvessels for implantation to promote angiogenesis. These approaches successfully showed significant enhancement in long-term survival and regenerative functions of implanted cells, yet there remains room for improvement.


      Methods: This paper suggests a proof-of-concept strategy to utilize novel scaffolds of dimpled/hollow electrospun fibers that enable the formation of highly mature pre-vasculatures with adequate dimensions and fast degrading in the tissue.


      Result: Higher surface roughness improved the maturity of endothelial cells mediated by increased cell-scaffold affinity. The degradation of scaffold material for functional restoration of the neo-vasculatures was also expedited by employing the hollow scaffold design based on co-axial electrospinning techniques.


      Conclusion: This unique scaffold-based pre-vasculature can hold implanted cells and tissue constructs for a prolonged time while minimizing the cellular loss, manifesting as a gold standard design for transplantable scaffolds.

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      참고문헌 (Reference)

      1 Kaully T, "Vascularization—the conduit to viable engineered tissues" 15 : 159-169, 2009

      2 Lovett M, "Vascularization strategies for tissue engineering" 15 : 353-370, 2009

      3 Song HG, "Vascular tissue engineering : progress, challenges, and clinical promise" 22 : 340-354, 2018

      4 Paulsen SJ, "Tissue vascularization through 3D printing:will technology bring us flow?" 244 : 629-640, 2015

      5 Birdsey GM, "The endothelial transcription factor ERG promotes vascular stability and growth through Wnt/b-catenin signaling" 32 : 82-96, 2015

      6 Thottappillil N, "Scaffolds in vascular regeneration : current status" 11 : 79-91, 2015

      7 Hamasaki N, "Red blood cell function and blood storage" 79 : 191-197, 2000

      8 Katsogiannis KAG, "Porous electrospun polycaprolactone(PCL)fibres by phase separation" 69 : 284-295, 2015

      9 Ferreri DM, "N-cadherin levels in endothelial cells are regulated by monolayer maturity and p120 availability" 15 : 333-349, 2008

      10 Hardy JD, "Landmark perspective. Transplantation of blood vessels, organs, and limbs" 250 : 954-957, 1983

      1 Kaully T, "Vascularization—the conduit to viable engineered tissues" 15 : 159-169, 2009

      2 Lovett M, "Vascularization strategies for tissue engineering" 15 : 353-370, 2009

      3 Song HG, "Vascular tissue engineering : progress, challenges, and clinical promise" 22 : 340-354, 2018

      4 Paulsen SJ, "Tissue vascularization through 3D printing:will technology bring us flow?" 244 : 629-640, 2015

      5 Birdsey GM, "The endothelial transcription factor ERG promotes vascular stability and growth through Wnt/b-catenin signaling" 32 : 82-96, 2015

      6 Thottappillil N, "Scaffolds in vascular regeneration : current status" 11 : 79-91, 2015

      7 Hamasaki N, "Red blood cell function and blood storage" 79 : 191-197, 2000

      8 Katsogiannis KAG, "Porous electrospun polycaprolactone(PCL)fibres by phase separation" 69 : 284-295, 2015

      9 Ferreri DM, "N-cadherin levels in endothelial cells are regulated by monolayer maturity and p120 availability" 15 : 333-349, 2008

      10 Hardy JD, "Landmark perspective. Transplantation of blood vessels, organs, and limbs" 250 : 954-957, 1983

      11 Chung TW, "Enhancement of the growth of human endothelial cells by surfaceroughness at nanometer sca" 24 : 4655-4661, 2003

      12 Jain RK, "Engineering vascularized tissue" 23 : 821-823, 2005

      13 Awad NK, "Electrospun fibrous scaffolds for small-diameter blood vessels : a review" 8 : 15-, 2018

      14 Perry L, "Elderly patient-derived endothelial cells for vascularization of engineered muscle" 25 : 935-948, 2017

      15 Norton KA, "Effects of endothelial cell proliferation and migration rates in a computational model of sprouting angiogenesis" 6 : 36992-, 2016

      16 Lee JB, "Development of 3D microvascular networks within gelatin hydrogels using thermoresponsive sacrificial microfibers" 5 : 781-785, 2016

      17 Inomata K, "Co-culture of osteoblasts and endothelial cells on a microfiber scaffold to construct bone-like tissue with vascular networks" 12 : 2869-, 2019

      18 Costa-Almeida R, "Cellular strategies to promote vasculaisation in tissue engineering applications" 28 : 51-67, 2014

      19 Ravi S, "Biomaterials for vascular tissue engineering" 5 : 107-120, 2010

      20 Kinstlinger IS, "3D-printed fluidic networks as vasculature for engineered tissue" 16 : 2025-2043, 2016

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      학술지등록 한글명 : 조직공학과 재생의학
      외국어명 : Tissue Engineering and Regenerative Medicine
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-10-01 평가 등재학술지 선정 (기타) KCI등재
      2012-01-01 평가 등재후보 1차 FAIL (기타) KCI등재후보
      2011-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2010-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2008-01-01 평가 SCIE 등재 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.08 0.42 0.81
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.69 0.51 0.367 0.03
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