| Literature DB >> 30561043 |
Nicholas Vaudreuil1, Karl Henrikson1, Pedro Pohl1,2, Andrew Lee1, Hang Lin1, Adam Olsen1, Qing Dong1, Malcolm Dombrowski1, James Kang3, Nam Vo1, Joon Lee1, Gwen Sowa1,4.
Abstract
Tissue engineering approaches to treatment of intervertebral disc degeneration (IDD) represent a novel avenue of addressing the biologic basis of this disease. However, such approaches remain limited by their invasive nature and disruption to the annular fibrosis (AF). This study sought to explore a new minimally-invasive tissue-engineering approach utilizing an injection of a photopolymerizable biogel scaffold seeded with mesenchymal stem cells (MSCs) directly into the nucleus pulposus (NP). This study was performed using rabbit specimens for both in vivo and in vitro outcome measures. The treatment in this study was performed by injecting 25 μl of 10% (w/v) methacrylated gelatin biogel with 0.15% (w/v) lithium phenyl 2,4,6-trimethylbenzoylphosphinate (LAP) and rabbit MSCs (1 × 106 ) cells/ml into the NP. Samples were then photopolymerized in situ using non-ultraviolet light irradiation via a fiberoptic wire. For the in vitro arm of this study, gene expression analysis demonstrated increased anabolic activity in irradiated MSCs with and without biogel scaffolds. For the in vivo arm of this study, while GAG analysis did not demonstrate significant differences between groups, MRI analysis exhibited a trend toward improved NP matrix. Histological analysis was consistent with increased cellularity and less severe disc degeneration in the MSC + Gel group. However, osteophyte formation was noted in both Stab and MSC + Gel groups after the study period. Increased matrix gene expression of irradiated groups within in vitro studies indicates a photobiologic effect of 405 nm light. Despite promising anabolic actions, osteophyte formation and AF defects could not be avoided with implementation of this minimally-invasive tissue-engineering approach.Entities:
Keywords: in vivo rabbit model; intervertebral disc degeneration; mesenchymal stem cells; minimally-invasive; tissue engineering
Year: 2019 PMID: 30561043 DOI: 10.1002/jor.24208
Source DB: PubMed Journal: J Orthop Res ISSN: 0736-0266 Impact factor: 3.494