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Engineered Disc-Like Angle-Ply Structures for Intervertebral Disc Replacement

2010; Lippincott Williams & Wilkins; Volume: 35; Issue: 8 Linguagem: Inglês

10.1097/brs.0b013e3181d74414

1528-1159

Nandan L. Nerurkar, Sounok Sen, Alice H. Huang, Dawn M. Elliott, Robert L. Mauck,

Medical Imaging and Analysis

In Brief Study Design. To develop a construction algorithm in which electrospun nanofibrous scaffolds are coupled with a biocompatible hydrogel to engineer a mesenchymal stem cell (MSC)-based disc replacement. Objective. To engineer a disc-like angle-ply structure (DAPS) that replicates the multiscale architecture of the intervertebral disc. Summary of Background Data. Successful engineering of a replacement for the intervertebral disc requires replication of its mechanical function and anatomic form. Despite many attempts to engineer a replacement for ailing and degenerated discs, no prior study has replicated the multiscale hierarchical architecture of the native disc, and very few have assessed the mechanical function of formed neo-tissues. Methods. A new algorithm for the construction of a disc analogue was developed, using agarose to form a central nucleus pulposus (NP) and oriented electrospun nanofibrous scaffolds to form the anulus fibrosus region (AF). Bovine MSCs were seeded into both regions and biochemical, histologic, and mechanical maturation were evaluated with in vitro culture. Results. We show that mechanical testing in compression and torsion, loading methods commonly used to assess disc mechanics, reveal equilibrium and time-dependent behaviors that are qualitatively similar to native tissue, although lesser in magnitude. Further, we demonstrate that cells seeded into both AF and NP regions adopt distinct morphologies that mirror those seen in native tissue, and that, in the AF region, this ordered community of cells deposit matrix that is organized in an angle-ply configuration. Finally, constructs demonstrate functional development with long-term in vitro culture. Conclusion. These findings provide a new approach for disc tissue engineering that replicates multi-scale form and function of the intervertebral disc, providing a foundation from which to build a multi-scale, biologic, anatomically and hierarchically relevant composite disc analogue for eventual disc replacement. Here, we describe a new algorithm for the engineering of an intervertebral disc, formed with mesenchymal stem cells and replicating key hierarchical features of the native tissue, including a gelatinous nucleus pulposus and a ±30° angle-ply multilamellar anulus fibrosus. Engineered disc constructs accrued matrix and improved mechanical properties with time in culture.