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A 3D bioprinted complex structure for engineering the muscle–tendon unit

356

Citations

26

References

2015

Year

TLDR

Three‑dimensional integrated organ printing (IOP) seeks to fabricate tissue constructs that mimic native tissues, and is especially suited for complex musculoskeletal tissues with regional differences in cell types and mechanical properties. The authors aim to use IOP to fabricate a single integrated muscle–tendon unit (MTU) construct by depositing four distinct components. They co‑printed thermoplastic polyurethane with C2C12‑laden hydrogel to create an elastic muscle side, and poly‑caprolactone with NIH/3T3‑laden hydrogel to produce a stiff tendon side. The resulting construct exhibited region‑specific mechanics (elastic PU‑C2C12 side, stiff PCL‑NIH/3T3 side, intermediate interface), >80 % cell viability at 1 and 7 days, and initial tissue development, demonstrating IOP’s versatility for MTU engineering.

Abstract

Three-dimensional integrated organ printing (IOP) technology seeks to fabricate tissue constructs that can mimic the structural and functional properties of native tissues. This technology is particularly useful for complex tissues such as those in the musculoskeletal system, which possess regional differences in cell types and mechanical properties. Here, we present the use of our IOP system for the processing and deposition of four different components for the fabrication of a single integrated muscle–tendon unit (MTU) construct. Thermoplastic polyurethane (PU) was co-printed with C2C12 cell-laden hydrogel-based bioink for elasticity and muscle development on one side, while poly(-caprolactone) (PCL) was co-printed with NIH/3T3 cell-laden hydrogel-based bioink for stiffness and tendon development on the other. The final construct was elastic on the PU-C2C12 muscle side (E = 0.39 ± 0.05 MPa), stiff on the PCL-NIH/3T3 tendon side (E = 46.67 ± 2.67 MPa) and intermediate in the interface region (E = 1.03 ± 0.14 MPa). These constructs exhibited >80% cell viability at 1 and 7 d after printing, as well as initial tissue development and differentiation. This study demonstrates the versatility of the IOP system to create integrated tissue constructs with region-specific biological and mechanical characteristics for MTU engineering.

References

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