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In vitro vascularization of a combined system based on a 3D printing technique.
Zhao, Xinru; Liu, Libiao; Wang, Jiayin; Xu, Yufan; Zhang, Weiming; Khang, Gilson; Wang, Xiaohong.
Affiliation
  • Zhao X; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China.
  • Liu L; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China.
  • Wang J; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China.
  • Xu Y; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China.
  • Zhang W; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China.
  • Khang G; Department of BIN Fusion Technology and Department of Polymer Nano Science Technology, Chonbuk National University, Jeonju, Korea.
  • Wang X; Key Laboratory for Advanced Materials Processing Technology, Ministry of Education and Center of Organ Manufacturing, Department of Mechanical Engineering, Tsinghua University, Beijing, China. wangxiaohong@tsinghua.edu.cn.
J Tissue Eng Regen Med ; 10(10): 833-842, 2016 10.
Article in En | MEDLINE | ID: mdl-24399638
ABSTRACT
A vital challenge in complex organ manufacturing is to vascularize large combined tissues. The aim of this study is to vascularize in vitro an adipose-derived stem cell (ADSC)/fibrin/collagen incorporated three-dimensional (3D) poly(d,l-lactic-co-glycolic acid) (PLGA) scaffold (10 × 10 × 10 mm3 ) with interconnected channels. A low-temperature 3D printing technique was employed to build the PLGA scaffold. A step-by-step cocktail procedure was designed to engage or steer the ADSCs in the PLGA channels towards both endothelial and smooth muscle cell lineages. The combined system had sufficient mechanical properties to support the cell/fibrin/collagen hydrogel inside the predefined PLGA channels. The ADSCs encapsulated in the fibrin/collagen hydrogel differentiated to endothelial and smooth muscle cell lineage, respectively, corresponding to their respective locations in the construct and formed vascular-like structures. This technique allows in vitro vascularization of the predefined PLGA channels and provides a choice for complex organ manufacture. Copyright © 2014 John Wiley & Sons, Ltd.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyglycolic Acid / Stem Cells / Fibrin / Adipose Tissue / Collagen / Neovascularization, Physiologic / Lactic Acid / Tissue Scaffolds Limits: Animals Language: En Journal: J Tissue Eng Regen Med Journal subject: BIOTECNOLOGIA / HISTOLOGIA Year: 2016 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyglycolic Acid / Stem Cells / Fibrin / Adipose Tissue / Collagen / Neovascularization, Physiologic / Lactic Acid / Tissue Scaffolds Limits: Animals Language: En Journal: J Tissue Eng Regen Med Journal subject: BIOTECNOLOGIA / HISTOLOGIA Year: 2016 Document type: Article Affiliation country: China