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<p>Formation of chondromimetic human mesenchymal stem cell (hMSC) condensations typically requires in vitro culture in defined environments. In addition, extended in vitro culture in differentiation media over several weeks is usually necessary prior to implantation, which is costly, time consuming, and delays clinical treatment. Here, this study reports on immediately implantable core/shell microgels with a high-density hMSC-laden core and rapidly degradable hydrogel shell. The hMSCs in the core-formed cell condensations within 12&#xa0;h and the oxidized and methacrylated alginate (OMA) hydrogel shells were completely degraded within 3&#xa0;days, enabling spontaneous and precipitous fusion of adjacent condensed aggregates. By delivering transforming growth factor-β1 (TGF-β1) within the core, the fused condensates were chondrogenically differentiated and formed cartilage-like microtissues. Importantly, these hMSC-laden core/shell microgels, fabricated without any in vitro culture, were subcutaneously implanted into mice and shown to form cartilage-like tissue via cellular condensations in the core after 3&#xa0;weeks. This innovative approach to form cell condensations in situ without in vitro culture that can fuse together with each other and with host tissue and mature into new tissue with incorporated bioactive signals allows for immediate implantation and may be a platform strategy for cartilage regeneration and other tissue engineering applications.</p>

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In situ cell condensation-based cartilage tissue engineering via immediately implantable high-density stem cell core and rapidly degradable shell microgels

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月12日

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  • Sang Jin Lee,
  • Oju Jeon,
  • Yu Bin Lee,
  • Daniel S. Alt,
  • Aixiang Ding,
  • Rui Tang,
  • Eben Alsberg

摘要

Formation of chondromimetic human mesenchymal stem cell (hMSC) condensations typically requires in vitro culture in defined environments. In addition, extended in vitro culture in differentiation media over several weeks is usually necessary prior to implantation, which is costly, time consuming, and delays clinical treatment. Here, this study reports on immediately implantable core/shell microgels with a high-density hMSC-laden core and rapidly degradable hydrogel shell. The hMSCs in the core-formed cell condensations within 12 h and the oxidized and methacrylated alginate (OMA) hydrogel shells were completely degraded within 3 days, enabling spontaneous and precipitous fusion of adjacent condensed aggregates. By delivering transforming growth factor-β1 (TGF-β1) within the core, the fused condensates were chondrogenically differentiated and formed cartilage-like microtissues. Importantly, these hMSC-laden core/shell microgels, fabricated without any in vitro culture, were subcutaneously implanted into mice and shown to form cartilage-like tissue via cellular condensations in the core after 3 weeks. This innovative approach to form cell condensations in situ without in vitro culture that can fuse together with each other and with host tissue and mature into new tissue with incorporated bioactive signals allows for immediate implantation and may be a platform strategy for cartilage regeneration and other tissue engineering applications.