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Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities

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Listed:
  • Amy Y. Clark

    (Georgia Institute of Technology
    Georgia Institute of Technology)

  • Karen E. Martin

    (Georgia Institute of Technology
    Georgia Institute of Technology)

  • José R. García

    (Georgia Institute of Technology
    Georgia Institute of Technology)

  • Christopher T. Johnson

    (Georgia Institute of Technology
    Georgia Tech and Emory)

  • Hannah S. Theriault

    (Georgia Institute of Technology
    Georgia Tech and Emory)

  • Woojin M. Han

    (Georgia Institute of Technology
    Georgia Institute of Technology)

  • Dennis W. Zhou

    (Georgia Institute of Technology
    Georgia Tech and Emory)

  • Edward A. Botchwey

    (Georgia Institute of Technology
    Georgia Tech and Emory)

  • Andrés J. García

    (Georgia Institute of Technology
    Georgia Institute of Technology)

Abstract

Stem cell therapies are limited by poor cell survival and engraftment. A hurdle to the use of materials for cell delivery is the lack of understanding of material properties that govern transplanted stem cell functionality. Here, we show that synthetic hydrogels presenting integrin-specific peptides enhance the survival, persistence, and osteo-reparative functions of human bone marrow-derived mesenchymal stem cells (hMSCs) transplanted in murine bone defects. Integrin-specific hydrogels regulate hMSC adhesion, paracrine signaling, and osteoblastic differentiation in vitro. Hydrogels presenting GFOGER, a peptide targeting α2β1 integrin, prolong hMSC survival and engraftment in a segmental bone defect and result in improved bone repair compared to other peptides. Integrin-specific hydrogels have diverse pleiotropic effects on hMSC reparative activities, modulating in vitro cytokine secretion and in vivo gene expression for effectors associated with inflammation, vascularization, and bone formation. These results demonstrate that integrin-specific hydrogels improve tissue healing by directing hMSC survival, engraftment, and reparative activities.

Suggested Citation

  • Amy Y. Clark & Karen E. Martin & José R. García & Christopher T. Johnson & Hannah S. Theriault & Woojin M. Han & Dennis W. Zhou & Edward A. Botchwey & Andrés J. García, 2020. "Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-14000-9
    DOI: 10.1038/s41467-019-14000-9
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    Cited by:

    1. Xunwu Hu & Sona Rani Roy & Chengzhi Jin & Guanying Li & Qizheng Zhang & Natsuko Asano & Shunsuke Asahina & Tomoko Kajiwara & Atsushi Takahara & Bolu Feng & Kazuhiro Aoki & Chenjie Xu & Ye Zhang, 2022. "Control cell migration by engineering integrin ligand assembly," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    2. Alisa H. Isaac & Sarea Y. Recalde Phillips & Elizabeth Ruben & Matthew Estes & Varsha Rajavel & Talia Baig & Carol Paleti & Kirsten Landsgaard & Ryang Hwa Lee & Teja Guda & Michael F. Criscitiello & C, 2024. "Impact of PEG sensitization on the efficacy of PEG hydrogel-mediated tissue engineering," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    3. Ye He & Shujie Yang & Pengzhan Liu & Ke Li & Ke Jin & Ryan Becker & Jinxin Zhang & Chuanchuan Lin & Jianping Xia & Zhehan Ma & Zhiteng Ma & Ruoyu Zhong & Luke P. Lee & Tony Jun Huang, 2023. "Acoustofluidic Interfaces for the Mechanobiological Secretome of MSCs," Nature Communications, Nature, vol. 14(1), pages 1-12, December.

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