4.8 Article

Nanoengineered Osteoinductive Bioink for 3D Bioprinting Bone Tissue

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 14, Pages 15976-15988

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b19037

Keywords

bone bioprinting; osteoinductive bioinks; nanomaterials; ionic-covalent reinforcement; hydrogels

Funding

  1. National Institute of Biomedical Imaging and Bioengineering (NIBIB) of the National Institutes of Health (NIH) [DP2 EB026265]
  2. National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) [R21 AR072292]
  3. National Science Foundation (NSF) [CBET 1705852]

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Bioprinting is an emerging additive manufacturing approach to the fabrication of patient-specific, implantable three-dimensional (3D) constructs for regenerative medicine. However, developing cell-compatible bioinks with high printability, structural stability, biodegradability, and bioactive characteristics is still a primary challenge for translating 3D bioprinting technology to preclinical and clinal models. To overcome this challenge, we developed a nanoengineered ionic covalent entanglement (NICE) bioink formulation for 3D bone bioprinting. The NICE bioinks allow precise control over printability, mechanical properties, and degradation characteristics, enabling custom 3D fabrication of mechanically resilient, cellularized structures. We demonstrate cell-induced remodeling of 3D bioprinted scaffolds over 60 days, demonstrating deposition of nascent extracellular matrix proteins. Interestingly, the bioprinted constructs induce endochondral differentiation of encapsulated human mesenchymal stem cells (hMSCs) in the absence of osteoinducing agent. Using next-generation transcriptome sequencing (RNA-seq) technology, we establish the role of nanosilicates, a bioactive component of NICE bioink, to stimulate endochondral differentiation at the transcriptome level. Overall, the osteoinductive bioink has the ability to induce formation of osteo-related mineralized extracellular matrix by encapsulated hMSCs in growth factor-free conditions. Furthermore, we demonstrate the ability of NICE bioink to fabricate patient-specific, implantable 3D scaffolds for repair of craniomaxillofacial bone defects. We envision development of this NICE bioink technology toward a realistic clinical process for 3D bioprinting patient-specific bone tissue for regenerative medicine.

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