Potential of Human Nucleus Pulposus-Like Cells Derived From Umbilical Cord to Treat Degenerative Disc Disease

被引:32
作者
Perez-Cruet, Mick [1 ,2 ,3 ,4 ]
Beeravolu, Naimisha [3 ,5 ]
McKee, Christina [3 ,5 ]
Brougham, Jared [2 ]
Khan, Irfan [3 ,5 ,6 ]
Bakshi, Shreeya [3 ,5 ]
Chaudhry, G. Rasul [3 ,5 ]
机构
[1] Beaumont Hlth Syst, Dept Neurosurg, Royal Oak, MI USA
[2] Oakland Univ, OUWB Sch Med, Rochester, MI 48063 USA
[3] OU WB Inst Stem Cell & Regenerat Med, Rochester, MI USA
[4] Michigan Head & Spine Inst, Southfield, MI USA
[5] Oakland Univ, Dept Biol Sci, 201 Meadow Brook Rd, Rochester, MI 48309 USA
[6] Univ Karachi, Int Ctr Chem & Biol Sci, Dr Panjwani Ctr Mol Med & Drug Res, Karachi, Pakistan
关键词
Cell therapy; Human umbilical cord mesenchyaml stem cells; Intervertebral disc; Nucleus pulposus; Rabbit model; TGFB pathway; Tissue engineering; MESENCHYMAL STEM-CELLS; INTERVERTEBRAL DISC; ANNULUS FIBROSUS; STROMAL CELLS; TRANSPLANTATION; MODEL; DIFFERENTIATION; REGENERATION; GENE; CHONDROCYTES;
D O I
10.1093/neuros/nyy012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND: Degenerative disc disease (DDD) is a common spinal disorder that manifests with neck and lower back pain caused by the degeneration of intervertebral discs (IVDs). Currently, there is no treatment to cure this debilitating ailment. OBJECTIVE: To investigate the potential of nucleus pulposus (NP)-like cells (NPCs) derived from human umbilical cord mesenchymal stem cells (MSCs) to restore degenerated IVDs using a rabbit DDD model. METHODS: NPCs differentiated from MSCs were characterized using quantitative real-time reverse transcription polymerase chain reaction and immunocytochemical analysis. MSCs and NPCs were labeled with fluorescent dye, PKH26, and transplanted into degenerated IVDs of a rabbit model of DDD (n = 9 each). Magnetic resonance imaging of the IVDs was performed before and after IVD degeneration, and following cell transplantation. IVDs were extracted 8 wk post-transplantation and analyzed by various biochemical, immunohistological, and molecular techniques. RESULTS: NPC derivatives of MSCs expressed known NP-specific genes, SOX9, ACAN, COL2, FOXF1, and KRT19. Transplanted cells survived, dispersed, and integrated into the degenerated IVDs. IVDs augmented with NPCs showed significant improvement in the histology, cellularity, sulfated glycosaminoglycan and water contents of the NP. In addition, expression of human genes, SOX9, ACAN, COL2, FOXF1, KRT19, PAX6, CA12, and COMP, as well as proteins, SOX9, ACAN, COL2, and FOXF1, suggest NP biosynthesis due to transplantation of NPCs. Based on these results, a molecular mechanism for NP regeneration was proposed. CONCLUSION: The findings of this study demonstrating feasibility and efficacy of NPCs to regenerate NP should spur interest for clinical studies to treat DDD using cell therapy.
引用
收藏
页码:272 / 283
页数:12
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