4.8 Article

Three-Dimensional Porous Scaffolds with Biomimetic Microarchitecture and Bioactivity for Cartilage Tissue Engineering

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 40, Pages 36359-36370

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b12206

Keywords

electrospun nanofiber; decellularized extracellular matrix; composite scaffold; shape memory; cartilage tissue engineering

Funding

  1. Key Technology Support Project of the Shanghai Municipal Science and Technology Commission [16441908200, 13441902900]
  2. Collaborative Innovation Project of Shanghai Jiao Tong University School of Medicine [TM201619]
  3. National Natural Science Foundation of China [81570089, 81970014]
  4. Natural Science Foundation of Shanghai [19ZR1442600]

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Ideal tissue-engineering cartilage scaffolds should possess the same nanofibrous structure as the microstructure of native cartilage as well as the same biological function provided by the microenvironment for neocartilage regeneration. In the present study, three-dimensional composite biomimetic scaffolds with different concentration ratios of electrospun gelatin-polycaprolactone (gelatin-PCL) nanofibers and decellularized cartilage extracellular matrix (DCECM) were fabricated. The nanofibers with the biomimetic microarchitecture of native cartilage served as a skeleton with excellent mechanical properties, and the DCECM served as a biological functionalization platform for the induction of cell response and the promotion of cartilage regeneration. Experimental results showed that the composite nanofiber/DCECM (NF/DCECM) scaffolds had stronger mechanical properties and structural stability in wet state compared with those of DCECM scaffolds. In vitro experiments demonstrated that all scaffolds had good biocompatibility, but the chondrocyte proliferation rate of the composite NF/DCECM scaffolds was higher than that of the NF scaffolds. In vitro and in vivo cartilage regeneration results indicated that the DCECM component of the composite scaffolds facilitated early maturation of the cartilage lacuna and the secretion of collagen and glycosaminoglycan. The macroscopic and histological results at 12 weeks postsurgery exhibited that the composite NF/ DCECM scaffolds yielded better cartilage repair outcomes than those of the nontreated group and NF scaffolds group. Overall, the present study demonstrated that the structurally and functionally biomimetic NF/DCECM scaffold is a promising tissue engineering scaffold for cartilage regeneration and cartilage defect repair.

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