Combination of Multifaceted Strategies to Maximize the Therapeutic Benefits of Neural Stem Cell Transplantation for Spinal Cord Repair

被引:50
|
作者
Hwang, Dong H. [1 ]
Kim, Hyuk M. [1 ]
Kang, Young M. [1 ]
Joo, In S. [2 ]
Cho, Chong-Su [3 ]
Yoon, Byung-Woo [4 ,5 ]
Kim, Seung U. [6 ,7 ]
Kim, Byung G. [1 ,2 ]
机构
[1] Ajou Univ, Sch Med, Brain Dis Res Ctr, Inst Med Sci, Suwon 443721, South Korea
[2] Ajou Univ, Sch Med, Dept Neurol, Suwon 443721, South Korea
[3] Seoul Natl Univ, Dept Agr Biotechnol, Seoul, South Korea
[4] Seoul Natl Univ Hosp, Dept Neurol, Clin Res Inst, Seoul 110744, South Korea
[5] Seoul Natl Univ Hosp, Dept Neurol, Neurosci Res Ctr, Seoul 110744, South Korea
[6] Univ British Columbia, Dept Neurol, Vancouver, BC V5Z 1M9, Canada
[7] Chung Ang Univ, Sch Med, Med Res Inst, Seoul, South Korea
关键词
Stem cells; Spinal cord injury (SCI); Tissue scaffold (Pclf polymer); Neurotrophin; 3; Motor evoked potential; Chondroitinase ABC; CHONDROITIN SULFATE PROTEOGLYCANS; RESTRICTED PRECURSOR CELLS; FUNCTIONAL RECOVERY; INJURY REPAIR; DELAYED TRANSPLANTATION; NEUROTROPHIC FACTORS; LOCOMOTOR RECOVERY; ENHANCES SURVIVAL; GROWTH-FACTOR; GENE-THERAPY;
D O I
10.3727/096368910X557155
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neural stem cells (NSCs) possess therapeutic potentials to reverse complex pathological processes following spinal cord injury (SCI), but many obstacles remain that could not be fully overcome by NSC transplantation alone. Combining complementary strategies might be required to advance NSC-based treatments to the clinical stage. The present study was undertaken to examine whether combination of NSCs, polymer scaffolds, neurotrophin-3 (NT3), and chondroitinase, which cleaves chondroitin sulfate proteoglycans at the interface between spinal cord and implanted scaffold, could provide additive therapeutic benefits. In a rat hemisection model, poly(E-caprolactone) (PCL) was used as a bridging scaffold and as a vehicle for NSC delivery. The PCL scaffolds seeded with F3 NSCs or NT3 overexpressing F3 cells (F3.NT3) were implanted into hemisected cavities. F3.NT3 showed better survival and migration, and more frequently differentiated into neurons and oligodendrocytes than F3 cells. Animals with PCL scaffold containing F3.NT3 cells showed the best locomotor recovery, and motor evoked potentials (MEPs) following transcranial magnetic stimulation were recorded only in PCL-F3.NT3 group in contralateral, but not ipsilateral, hindlimbs. Implantation of PCL scaffold with F3.NT3 cells increased NT3 levels, promoted neuroplasticity, and enhanced remyelination of contralateral white matter. Combining chondroitinase treatment after PCL-F3.NT3 implantation further enhanced cell migration and promoted axonal remodeling, and this was accompanied by augmented locomotor recovery and restoration of MEPs in ipsilateral hindlimbs. We demonstrate that combining multifaceted strategies can maximize the therapeutic benefits of NSC transplantation for SCI. Our results may have important clinical implications for the design of future NSC-based strategies.
引用
收藏
页码:1361 / 1379
页数:19
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