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Human Cartilage Tissue Fabrication Using Three-dimensional Inkjet Printing Technology
Published on: June 10, 2014
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Three-Dimensional Printing Biologically Inspired DNA-Based Gradient Scaffolds for Cartilage Tissue Regeneration
Xuan Zhou, Sara Tenaglio, Timothy Esworthy
1Department of Chemical Engineering, Northeastern University, Boston, Massachusetts 02115, United States.
ACS Applied Materials & Interfaces
|July 1, 2020
Summary
This study developed a novel 3D-printed scaffold using lysine-functionalized rosette nanotubes (RNTK) to enhance cartilage repair. The RNTK-enhanced scaffold significantly boosted adipose-derived mesenchymal stem cell (ADSC) chondrogenic differentiation and cartilage matrix production.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Cartilage damage from aging, injury, or disease leads to pain and disability due to cartilage's poor regenerative capacity.
- Current treatments like autografts and allografts face limitations such as donor scarcity and immune rejection.
- Engineered tissues offer a promising alternative for cartilage repair and regeneration.
Purpose of the Study:
- To develop a three-dimensional (3D) printed, three-layer gradient scaffold incorporating lysine-functionalized rosette nanotubes (RNTK).
- To enhance the chondrogenic differentiation of adipose-derived mesenchymal stem cells (ADSCs) on the novel scaffold.
- To evaluate the scaffold's potential for cartilage repair and regeneration.
Main Methods:
- Fabrication of a three-layer gradient scaffold using gelatin methacrylate (GelMA) and poly(ethylene glycol) diacrylate (PEGDA) via stereolithography.
- Functionalization of the scaffold surface with lysine-functionalized rosette nanotubes (RNTK).
- Culturing ADSCs on the GelMA-PEGDA-RNTK scaffold and assessing cell proliferation, chondrogenic differentiation markers (collagen II, glycosaminoglycan, total collagen), and gene expression.
Main Results:
- The GelMA-PEGDA-RNTK scaffold showed a 34% increase in ADSC population compared to the control scaffold.
- Significant increases in collagen II (59%), glycosaminoglycan (71%), and total collagen (60%) synthesis were observed after 3 weeks of chondrogenic differentiation.
- Gene expression of collagen II α1, SOX 9, and aggrecan increased by 79%, 52%, and 47%, respectively, on the RNTK-enhanced scaffold.
Conclusions:
- Lysine-functionalized rosette nanotubes (RNTK) show significant potential in promoting chondrogenic differentiation.
- The 3D-printed three-layer gradient GelMA-PEGDA-RNTK scaffold is a promising biomaterial for cartilage repair and regeneration.
- This engineered scaffold offers a viable alternative to current cartilage repair strategies, addressing limitations of donor availability and immune rejection.

