4.8 Article

Patterned, organoid-based cartilaginous implants exhibit zone specific functionality forming osteochondral-like tissues in vivo

Journal

BIOMATERIALS
Volume 273, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2021.120820

Keywords

Tissue engineering; Osteochondral; Induced pluripotent stem cells; Organoid; Patterned implant

Funding

  1. Research Foundation Flanders (FWO) [1S05116 N, 12O7916 N, CARTiPLEX: G0A4718 N]
  2. European Research Council under the European Union's Seventh Framework Program (FP/2007-2013)/ERC [249191]
  3. European Research Council under the Horizon 2020 Framework Program (H2020/2014-2021)/ERC [772418]
  4. special research fund of the KU Leuven [GOA/13/016, C24/17/077]
  5. BONE Interreg North West Europe [NWE 497]
  6. European Regional Development Fund
  7. Horizon 2020 Framework Program Jointrpomise ((H2020-EU.3.1.3) [874837]
  8. Regenerative Medicine Crossing Borders REGMEDXB by EWI Flanders
  9. Hercules Foundation [AKUL/13/47]

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The study introduces a tissue engineering strategy using distinct cartilaginous organoids as building blocks to create a pre-engineered zonal pattern in constructs. By assembling different functional building blocks, complex tissue engineered implants with specific functionalities can be produced.
Tissue engineered constructs have the potential to respond to the unmet medical need of treating deep osteochondral defects. However, current tissue engineering strategies struggle in the attempt to create patterned constructs with biologically distinct functionality. In this work, a developmentally-inspired modular approach is proposed, whereby distinct cartilaginous organoids are used as living building blocks. First, a hierarchical construct was created, composed of three layers of cartilaginous tissue intermediates derived from human periosteum-derived cells: (i) early (SOX9), (ii) mature (COL2) and (iii) (pre)hypertrophic (IHH, COLX) phenotype. Subcutaneous implantation in nude mice generated a hybrid tissue containing one mineralized and one non-mineralized part. However, the non-mineralized part was represented by a collagen type I positive fibrocartilage-like tissue. To engineer a more stable articular cartilage part, iPSC-derived cartilage microtissues (SOX9, COL2; IHH neg) were generated. Subcutaneous implantation of assembled iPSC-derived cartilage microtissues resulted in a homogenous cartilaginous tissue positive for collagen type II but negative for osteocalcin. Finally, iPSC-derived cartilage microtissues in combination with the pre-hypertrophic cartilage organoids (IHH, COLX) could form dual tissues consisting of i) a cartilaginous safranin O positive and ii) a bony osteocalcin positive region upon subcutaneous implantation, corresponding to the pre-engineered zonal pattern. The assembly of functional building blocks, as presented in this work, opens possibilities for the production of complex tissue engineered implants by embedding zone-specific functionality through the use of pre-programmed living building blocks.

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