3D-Printed ABS and PLA Scaffolds for Cartilage and Nucleus Pulposus Tissue Regeneration

被引:262
作者
Rosenzweig, Derek H. [1 ,2 ]
Carelli, Eric [1 ]
Steffen, Thomas [1 ,2 ]
Jarzem, Peter [2 ]
Haglund, Lisbet [1 ,2 ,3 ]
机构
[1] McGill Univ, Dept Surg, Orthoped Res Lab, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Dept Surg, McGill Scoliosis & Spine Grp, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Ctr Hlth, Dept Surg, Montreal Gen Hosp, Montreal, PQ H3G 1A4, Canada
基金
加拿大健康研究院;
关键词
3D printing; chondrocyte; nucleus pulposus; intervertebral disc; PLA; ABS; tissue engineering; ARTICULAR-CARTILAGE; INTERVERTEBRAL-DISK; ANNULUS FIBROSUS; STEM-CELLS; DEGENERATION; MATRIX; DIFFERENTIATION; COMPRESSION; CULTURE; OSTEOARTHRITIS;
D O I
10.3390/ijms160715118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Painful degeneration of soft tissues accounts for high socioeconomic costs. Tissue engineering aims to provide biomimetics recapitulating native tissues. Biocompatible thermoplastics for 3D printing can generate high-resolution structures resembling tissue extracellular matrix. Large-pore 3D-printed acrylonitrile butadiene styrene (ABS) and polylactic acid (PLA) scaffolds were compared for cell ingrowth, viability, and tissue generation. Primary articular chondrocytes and nucleus pulposus (NP) cells were cultured on ABS and PLA scaffolds for three weeks. Both cell types proliferated well, showed high viability, and produced ample amounts of proteoglycan and collagen type II on both scaffolds. NP generated more matrix than chondrocytes; however, no difference was observed between scaffold types. Mechanical testing revealed sustained scaffold stability. This study demonstrates that chondrocytes and NP cells can proliferate on both ABS and PLA scaffolds printed with a simplistic, inexpensive desktop 3D printer. Moreover, NP cells produced more proteoglycan than chondrocytes, irrespective of thermoplastic type, indicating that cells maintain individual phenotype over the three-week culture period. Future scaffold designs covering larger pore sizes and better mimicking native tissue structure combined with more flexible or resorbable materials may provide implantable constructs with the proper structure, function, and cellularity necessary for potential cartilage and disc tissue repair in vivo.
引用
收藏
页码:15118 / 15135
页数:18
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