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3D Printed Cartilage-Like Tissue Constructs with Spatially Controlled Mechanical Properties.
de Melo, Bruna A G; Jodat, Yasamin A; Mehrotra, Shreya; Calabrese, Michelle A; Kamperman, Tom; Mandal, Biman B; Santana, Maria H A; Alsberg, Eben; Leijten, Jeroen; Shin, Su Ryon.
Affiliation
  • de Melo BAG; Division of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, USA.
  • Jodat YA; Division of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, USA.
  • Mehrotra S; Division of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, USA.
  • Calabrese MA; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
  • Kamperman T; Department of Developmental BioEngineering, University of Twente, Enschede, Overijssel 7522 NB, The Netherlands.
  • Mandal BB; Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati 781039, India.
  • Santana MHA; Department of Engineering of Materials and Bioprocesses School of Chemical Engineering, University of Campinas, Campinas, SP 13083-852, Brazil.
  • Alsberg E; Departments of Bioengineering and Orthopaedics, University of Illinois, Chicago, IL 60607, USA.
  • Leijten J; Department of Developmental BioEngineering, University of Twente, Enschede, Overijssel 7522 NB, The Netherlands.
  • Shin SR; Division of Engineering in Medicine, Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Cambridge, MA 02139, USA.
Adv Funct Mater ; 29(51)2019 Dec 19.
Article in En | MEDLINE | ID: mdl-34108852
ABSTRACT
Developing biomimetic cartilaginous tissues that support locomotion while maintaining chondrogenic behavior is a major challenge in the tissue engineering field. Specifically, while locomotive forces demand tissues with strong mechanical properties, chondrogenesis requires a soft microenvironment. To address this challenge, 3D cartilage-like tissue is bioprinted using two biomaterials with different mechanical properties a hard biomaterial to reflect the macromechanical properties of native cartilage, and a soft biomaterial to create a chondrogenic microenvironment. To this end, a hard biomaterial (MPa order compressive modulus) composed of an interpenetrating polymer network (IPN) of polyethylene glycol (PEG) and alginate hydrogel is developed as an extracellular matrix (ECM) with self-healing properties, but low diffusive capacity. Within this bath supplemented with thrombin, fibrinogen containing human mesenchymal stem cell (hMSC) spheroids is bioprinted forming fibrin, as the soft biomaterial (kPa order compressive modulus) to simulate cartilage's pericellular matrix and allow a fast diffusion of nutrients. The bioprinted hMSC spheroids improve viability and chondrogenic-like behavior without adversely affecting the macromechanical properties of the tissue. Therefore, the ability to print locally soft and cell stimulating microenvironments inside of a mechanically robust hydrogel is demonstrated, thereby uncoupling the micro- and macromechanical properties of the 3D printed tissues such as cartilage.
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