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Molecularly cleavable bioinks facilitate high-performance digital light processing-based bioprinting of functional volumetric soft tissues

Author

Listed:
  • Mian Wang

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Wanlu Li

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Jin Hao

    (Harvard University
    Harvard University
    Broad Institute of MIT and Harvard)

  • Arthur Gonzales

    (University of the Philippines Diliman)

  • Zhibo Zhao

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Regina Sanchez Flores

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Xiao Kuang

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Xuan Mu

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Terry Ching

    (Brigham and Women’s Hospital, Harvard Medical School
    Singapore University of Technology and Design
    Singapore University of Technology and Design
    National University of Singapore)

  • Guosheng Tang

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Zeyu Luo

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Carlos Ezio Garciamendez-Mijares

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Jugal Kishore Sahoo

    (Tufts University)

  • Michael F. Wells

    (Harvard University
    Harvard University
    Broad Institute of MIT and Harvard)

  • Gengle Niu

    (Harvard University
    Harvard University)

  • Prajwal Agrawal

    (Brigham and Women’s Hospital, Harvard Medical School)

  • Alfredo Quiñones-Hinojosa

    (Mayo Clinic)

  • Kevin Eggan

    (Harvard University
    Harvard University
    Broad Institute of MIT and Harvard)

  • Yu Shrike Zhang

    (Brigham and Women’s Hospital, Harvard Medical School
    Harvard University)

Abstract

Digital light processing bioprinting favors biofabrication of tissues with improved structural complexity. However, soft-tissue fabrication with this method remains a challenge to balance the physical performances of the bioinks for high-fidelity bioprinting and suitable microenvironments for the encapsulated cells to thrive. Here, we propose a molecular cleavage approach, where hyaluronic acid methacrylate (HAMA) is mixed with gelatin methacryloyl to achieve high-performance bioprinting, followed by selectively enzymatic digestion of HAMA, resulting in tissue-matching mechanical properties without losing the structural complexity and fidelity. Our method allows cellular morphological and functional improvements across multiple bioprinted tissue types featuring a wide range of mechanical stiffness, from the muscles to the brain, the softest organ of the human body. This platform endows us to biofabricate mechanically precisely tunable constructs to meet the biological function requirements of target tissues, potentially paving the way for broad applications in tissue and tissue model engineering.

Suggested Citation

  • Mian Wang & Wanlu Li & Jin Hao & Arthur Gonzales & Zhibo Zhao & Regina Sanchez Flores & Xiao Kuang & Xuan Mu & Terry Ching & Guosheng Tang & Zeyu Luo & Carlos Ezio Garciamendez-Mijares & Jugal Kishore, 2022. "Molecularly cleavable bioinks facilitate high-performance digital light processing-based bioprinting of functional volumetric soft tissues," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31002-2
    DOI: 10.1038/s41467-022-31002-2
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    References listed on IDEAS

    as
    1. Eneko Axpe & Gorka Orive & Kristian Franze & Eric A. Appel, 2020. "Towards brain-tissue-like biomaterials," Nature Communications, Nature, vol. 11(1), pages 1-4, December.
    2. Hong-Jen Lee & Chien-Feng Li & Diane Ruan & Jiabei He & Emily D. Montal & Sonja Lorenz & Geoffrey D. Girnun & Chia-Hsin Chan, 2019. "Non-proteolytic ubiquitination of Hexokinase 2 by HectH9 controls tumor metabolism and cancer stem cell expansion," Nature Communications, Nature, vol. 10(1), pages 1-16, December.
    3. Jiaxing Gong & Carl C. L. Schuurmans & Anne Metje van Genderen & Xia Cao & Wanlu Li & Feng Cheng & Jacqueline Jialu He & Arturo López & Valentin Huerta & Jennifer Manríquez & Ruiquan Li & Hongbin Li &, 2020. "Complexation-induced resolution enhancement of 3D-printed hydrogel constructs," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
    4. Jeff A. Stogsdill & Juan Ramirez & Di Liu & Yong Ho Kim & Katherine T. Baldwin & Eray Enustun & Tiffany Ejikeme & Ru-Rong Ji & Cagla Eroglu, 2017. "Astrocytic neuroligins control astrocyte morphogenesis and synaptogenesis," Nature, Nature, vol. 551(7679), pages 192-197, November.
    5. Douglas J. Bakkum & Urs Frey & Milos Radivojevic & Thomas L. Russell & Jan Müller & Michele Fiscella & Hirokazu Takahashi & Andreas Hierlemann, 2013. "Tracking axonal action potential propagation on a high-density microelectrode array across hundreds of sites," Nature Communications, Nature, vol. 4(1), pages 1-12, October.
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    Cited by:

    1. Yangteng Ou & Shixiang Cao & Yang Zhang & Hongjia Zhu & Chengzhi Guo & Wei Yan & Fengxue Xin & Weiliang Dong & Yanli Zhang & Masashi Narita & Ziyi Yu & Tuomas P. J. Knowles, 2023. "Bioprinting microporous functional living materials from protein-based core-shell microgels," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

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