Abstract

We had previously demonstrated the feasibility of preparing a centimeter-sized bone tissue construct by following a modular approach. In the present study, the objectives were to evaluate osteogenesis and tissue formation of human amniotic mesenchymal stem cells-laden CultiSpher S microcarriers during in vitro perfusion culture and after subcutaneous implantation. Microtissues were prepared in dynamic culture using spinner flasks in 28 days. In comparison with 1-week perfusion culture, microtissues became more obviously fused, demonstrating significantly higher cellularity, metabolic activity, ALP activity and calcium content while maintaining cell viability after 2-week perfusion. After subcutaneous implantation in nude mice for 6 and 12 weeks, all explants showed tight contexture, suggesting profound tissue remodeling in vivo. In addition, 12-week implantation resulted in slightly better tissue properties. However, in vitro perfusion culture time exerted great influence on the properties of corresponding explants. Degradation of microcarriers was more pronounced in the explants of 2-week perfused macrotissues compared to those of 1-week perfusion and directly implanted microtissues. Moreover, more blood vessel infiltration and bone matrix deposition with homogeneous spatial distribution were found in the explants of 2-week perfused macrotissues. Taken together, in vitro perfusion culture time is critical in engineering bone tissue replacements using such a modular approach, which holds great promise for bone regeneration.

Highlights

  • Tissue engineering aims at fabricating viable tissue replacements to repair and restore structure and function of damaged tissues by employing scaffolds and cells [1]

  • How in vitro perfusion culture time would affect tissue properties and how the osteogenesis of in vitro assembled tissues would be in vivo have not been evaluated

  • Microtissues were assembled in perfusion culture for 1 or 2 weeks and macrotissues were implanted into subcutaneous pockets of nude mice for 6 or 12 weeks to evaluate ectopic osteogenesis

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Summary

Introduction

Tissue engineering aims at fabricating viable tissue replacements to repair and restore structure and function of damaged tissues by employing scaffolds and cells [1]. Dynamic culture in bioreactors does not change the mechanism of mass transport inside constructs with high cellularity, which is essentially passive diffusion [8,9]. Another potential strategy is to build in a functional vascular network in in vitro engineered tissues, which is expected to quickly establish anastomosis with hosts once implanted [10]

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