Bionic tracheal tissue regeneration using a ring-shaped scaffold comprised of decellularized cartilaginous matrix and silk fibroin

被引:30
作者
Gao, Erji [1 ]
Li, Gao [3 ]
Cao, Runfeng [1 ,5 ]
Xia, Huitang [2 ]
Xu, Yong [1 ]
Jiang, Gening [1 ]
Xiao, Kaiyan [2 ]
Chen, Jie [2 ]
Chen, Ru [4 ]
Duan, Liang [1 ]
机构
[1] Tongji Univ, Shanghai Pulm Hosp, Sch Med, Dept Thorac Surg, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Anesthesiol, Shanghai Key Lab Tissue Engn,Sch Med, Shanghai, Peoples R China
[3] Hainan Med Univ, Dept Thorac Surg, Hainan Gen Hosp, Hainan Affiliated Hosp, Haikou, Hainan, Peoples R China
[4] Hainan Med Univ, Dept Breast, Hainan Gen Hosp, Hainan Affiliated Hosp, Haikou, Hainan, Peoples R China
[5] Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Dept Cardiothorac Surg, Shanghai, Peoples R China
基金
海南省自然科学基金; 中国国家自然科学基金; 上海市自然科学基金;
关键词
Cartilaginous ring; Bionic trachea; Decellularized cartilaginous matrix; Silk fibroin; Bone marrow stem cells; STROMAL CELLS; CROSS-LINKING; CHONDROGENIC DIFFERENTIATION; ENGINEERED TRACHEA; STEM-CELLS; CHONDROCYTES; PROLIFERATION;
D O I
10.1016/j.compositesb.2021.109470
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Reconstruction of full-circumferential segmental tracheal defect remains an international dilemma and the key challenge is the lack of a bionic tracheal substitute, with a specific configuration of cartilaginous rings inter-spersed with vascularized fibrous tissue (CRVFT). We previously demonstrated the formation of a bionic tracheal substitute with CRVFT in-vivo. However, it is still desirable to develop a scaffold with proper mechanical strength and chondroinductive activity to promote in-vivo cartilage formation, which could circumvent the painstaking procedure of in-vitro cultivation. Herein, we prepared a ring-shaped porous silk fibroin (SF)-rein-forced decellularized cartilaginous matrix (DCM) (DCM/SF) scaffold, which displayed suitable pore size (206.7 +/- 12.5 mu m) and porosity (92.7 +/- 2.5%) and was biocompatible for cell colonization. The addition of SF considerable enhanced anti-contraction capacity and Young's modulus, while diminishing water absorption and degradation rate of the DCM/SF scaffold. Further, the DCM/SF scaffold obviously promoted chondrogenesis of the embedded bone marrow stem cells (BMSCs), compared to DCM or SF scaffold alone. In addition, a cartilaginous ring was formed using the DCM/SF scaffold, which was repopulated with BMSCs after subcutaneous implantation in nude mouse. Moreover, a bionic tracheal tissue with remarkable CRVFT was achieved via the interrupted stacking of BMSC-DCM/SF constructs on a stent, before subcutaneous implantation into a rabbit for 4 weeks. The bionic trachea was fully revascularized and displayed comparable biochemical compositions and mechanical strength resembling to those of normal trachea. This study introduces a reliable new approach for bionic tracheal tissue regeneration and significantly advances the ongoing repair of segmental tracheal defect.
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页数:13
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