Volume 5, Issue 8 pp. e179-e187
Research Article

Biomimetic method for combining the nucleus pulposus and annulus fibrosus for intervertebral disc tissue engineering

Mihael Lazebnik

Mihael Lazebnik

Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, KS, USA

Search for more papers by this author
Milind Singh

Milind Singh

Department of Bioengineering, Rice University, Houston, TX, USA

Search for more papers by this author
Paul Glatt

Paul Glatt

Department of Biomedical Engineering, St. Louis University, St. Louis, MO, USA

Search for more papers by this author
Lisa A. Friis

Lisa A. Friis

Department of Mechanical Engineering, University of Kansas, Lawrence, KS, USA

Search for more papers by this author
Cory J. Berkland

Cory J. Berkland

Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, KS, USA

Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS, USA

Search for more papers by this author
Michael S. Detamore

Corresponding Author

Michael S. Detamore

Department of Chemical and Petroleum Engineering, University of Kansas, Lawrence, KS, USA

University of Kansas, Department of Chemical and Petroleum Engineering, 4132 Learned Hall, 1530 West 15th Street, Lawrence, KS 66045, USA.Search for more papers by this author
First published: 25 February 2011
Citations: 56

Abstract

Tissue engineering strategies for the intervertebral disc (IVD) have traditionally focused either on the annulus fibrosus (AF) or the nucleus pulposus (NP) in isolation, or have simply compared AF cells and NP cells in identical culture conditions. Recently, others in the field have become aware of the advantage of combining the AF and NP into a more comprehensive strategy to address IVD tissue engineering, and have introduced biomimetic approaches to either AF or NP tissue engineering. Here, we introduced a new method for developing a biomimetic, cell-seeded IVD by electrospinning circumferentially-orientated polycaprolactone fibres (AF analogue), seeding them with cells (porcine chondrocytes) and then gelling a cell–agarose solution in the centre (NP analogue). Scanning electron microscopy images demonstrated a high degree of fibre alignment and, along with fluorescent actin staining, confirmed a preferred orientation of cells in the direction of the fibres. Viability assays and histology collectively demonstrated that cells were viable and well-distributed around the interface between the NP and AF regions. In addition, mechanical testing confirmed that the composite IVD scaffolds had higher moduli than the agarose hydrogels alone. As we enter the new decade and the fields of AF and NP tissue engineering begin to merge into a new interfacial and functional IVD tissue-engineering field, approaches such as the method presented here will serve as the foundation for continuously advancing technology that we ultimately endeavour to bring to the clinic for the treatment of patients severely afflicted by degenerative disc disease. Copyright © 2011 John Wiley & Sons, Ltd.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.