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Leaf-venation-directed cellular alignment for macroscale cardiac constructs with tissue-like functionalities

Author

Listed:
  • Mao Mao

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Xiaoli Qu

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Yabo Zhang

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Bingsong Gu

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Chen Li

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Rongzhi Liu

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Xiao Li

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Hui Zhu

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Jiankang He

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

  • Dichen Li

    (Xi’an Jiaotong University
    Xi’an Jiaotong University)

Abstract

Recapitulating the complex structural, mechanical, and electrophysiological properties of native myocardium is crucial to engineering functional cardiac tissues. Here, we report a leaf-venation-directed strategy that enables the compaction and remodeling of cell-hydrogel hybrids into highly aligned and densely packed organizations in predetermined patterns. This strategy contributes to interconnected tubular structures with cell alignment along the hierarchical channels. Compared to randomly-distributed cells, the engineered leaf-venation-directed-cardiac tissues from neonatal rat cardiomyocytes manifest advanced maturation and functionality as evidenced by detectable electrophysiological activity, macroscopically synchronous contractions, and upregulated maturation genes. As a demonstration, human induced pluripotent stem cell-derived leaf-venation-directed-cardiac tissues are engineered with evident structural and functional improvement over time. With the elastic scaffolds, leaf-venation-directed tissues are assembled into 3D centimeter-scale cardiac constructs with programmed mechanical properties, which can be delivered through tubing without affecting cell viability. The present strategy may generate cardiac constructs with multifaceted functionalities to meet clinical demands.

Suggested Citation

  • Mao Mao & Xiaoli Qu & Yabo Zhang & Bingsong Gu & Chen Li & Rongzhi Liu & Xiao Li & Hui Zhu & Jiankang He & Dichen Li, 2023. "Leaf-venation-directed cellular alignment for macroscale cardiac constructs with tissue-like functionalities," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-37716-1
    DOI: 10.1038/s41467-023-37716-1
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    References listed on IDEAS

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    1. Ilya Y. Shadrin & Brian W. Allen & Ying Qian & Christopher P. Jackman & Aaron L. Carlson & Mark E. Juhas & Nenad Bursac, 2017. "Cardiopatch platform enables maturation and scale-up of human pluripotent stem cell-derived engineered heart tissues," Nature Communications, Nature, vol. 8(1), pages 1-15, December.
    2. Robert D. Kirkton & Nenad Bursac, 2011. "Engineering biosynthetic excitable tissues from unexcitable cells for electrophysiological and cell therapy studies," Nature Communications, Nature, vol. 2(1), pages 1-9, September.
    3. Sarah McLaughlin & Brian McNeill & James Podrebarac & Katsuhiro Hosoyama & Veronika Sedlakova & Gregory Cron & David Smyth & Richard Seymour & Keshav Goel & Wenbin Liang & Katey J. Rayner & Marc Ruel , 2019. "Injectable human recombinant collagen matrices limit adverse remodeling and improve cardiac function after myocardial infarction," Nature Communications, Nature, vol. 10(1), pages 1-14, December.
    4. Kacey Ronaldson-Bouchard & Stephen P. Ma & Keith Yeager & Timothy Chen & LouJin Song & Dario Sirabella & Kumi Morikawa & Diogo Teles & Masayuki Yazawa & Gordana Vunjak-Novakovic, 2018. "Advanced maturation of human cardiac tissue grown from pluripotent stem cells," Nature, Nature, vol. 556(7700), pages 239-243, April.
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