An Injectable Hyaluronan–Methylcellulose (HAMC) Hydrogel Combined with Wharton’s Jelly-Derived Mesenchymal Stromal Cells (WJ-MSCs) Promotes Degenerative Disc Repair
Authors:
- Un Yong ChoiUCUn Yong Choi
- Hari Prasad JoshiHari Prasad Joshi
- Samantha PayneSamantha Payne
- Kyoung Tae KimKKKyoung Tae Kim
- Jae Won KyungJKJae Won Kyung
- Hyemin ChoiHCHyemin Choi
- Michael J. CookeMCMichael J. Cooke
- Su Yeon KwonSKSu Yeon Kwon
- Eun Ji RohEREun Ji Roh
- Seil SohnSSSeil Sohn
- Molly S. ShoichetMolly S. Shoichet
- Inbo HanInbo Han
Open Access
- 7 October 2020
- journal article
- research article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 21 (19) , 7391
Abstract
Intervertebral disc (IVD) degeneration is one of the predominant causes of chronic low back pain (LBP), which is a leading cause of disability worldwide. Despite substantial progress in cell therapy for the treatment of IVD degeneration, significant challenges remain for clinical application. Here, we investigated the effectiveness of hyaluronan–methylcellulose (HAMC) hydrogels loaded with Wharton’s Jelly-derived mesenchymal stromal cell (WJ-MSCs) in vitro and in a rat coccygeal IVD degeneration model. Following induction of injury-induced IVD degeneration, female Sprague-Dawley rats were randomized into four groups to undergo a single intradiscal injection of the following: (1) phosphate buffered saline (PBS) vehicle, (2) HAMC, (3) WJ-MSCs (2 × 104 cells), and (4) WJ-MSCs-loaded HAMC (WJ-MSCs/HAMC) (n = 10/each group). Coccygeal discs were removed following sacrifice 6 weeks after implantation for radiologic and histologic analysis. We confirmed previous findings that encapsulation in HAMC increases the viability of WJ-MSCs for disc repair. The HAMC gel maintained significant cell viability in vitro. In addition, combined implantation of WJ-MSCs and HAMC significantly promoted degenerative disc repair compared to WJ-MSCs alone, presumably by improving nucleus pulposus cells viability and decreasing extracellular matrix degradation. Our results suggest that WJ-MSCs-loaded HAMC promotes IVD repair more effectively than cell injection alone and supports the potential clinical use of HAMC for cell delivery to arrest IVD degeneration or to promote IVD regeneration.Keywords
Funding Information
- Korea Health Technology Research and Development Project, Ministry of Health and Welfare Affairs (HR16C0002, HI16C0106, and HI20C0579)
This publication has 55 references indexed in Scilit:
- Wharton’s Jelly-Derived Mesenchymal Stem Cells: Phenotypic Characterization and Optimizing Their Therapeutic Potential for Clinical ApplicationsInternational Journal of Molecular Sciences, 2013
- Pathophysiology, diagnosis, and treatment of discogenic low back painWorld Journal of Orthopedics, 2013
- Characterization of hyaluronan–methylcellulose hydrogels for cell delivery to the injured spinal cordJournal of Biomedical Materials Research Part A, 2012
- Improving Viability of Stem Cells During Syringe Needle Flow Through the Design of Hydrogel Cell CarriersTissue Engineering Part A, 2012
- Pro-Inflammatory Cytokines, IFNγ and TNFα, Influence Immune Properties of Human Bone Marrow and Wharton Jelly Mesenchymal Stem Cells DifferentiallyPLOS ONE, 2010
- Long-Term Expansion and Pluripotent Marker Array Analysis of Wharton’s Jelly-Derived Mesenchymal Stem CellsStem Cells and Development, 2010
- Accelerated release of a sparingly soluble drug from an injectable hyaluronan–methylcellulose hydrogelJournal of Controlled Release, 2009
- A New Paradigm for Local and Sustained Release of Therapeutic Molecules to the Injured Spinal Cord for Neuroprotection and Tissue RepairTissue Engineering Part A, 2009
- Intervertebral Disc Tissue Engineering Using a Novel Hyaluronic Acid–Nanofibrous Scaffold (HANFS) AmalgamTissue Engineering Part A, 2008
- Accelerated cellular senescence in degenerate intervertebral discs: a possible role in the pathogenesis of intervertebral disc degenerationArthritis Research & Therapy, 2007