Effect of Schwann cell transplantation combined with electroacupuncture on axonal regeneration and remyelination in rats with spinal cord injury

被引:11
作者
Tan, Chengfang [1 ]
Yang, Cheng [1 ]
Liu, Hui [2 ]
Tang, Chenglin [1 ]
Huang, Siqin [1 ]
机构
[1] Chongqing Med Univ, Tradit Chinese Med Coll, 1 Yixueyuan Rd, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Inst Neurosci, Chongqing, Peoples R China
来源
ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY | 2021年 / 304卷 / 11期
基金
中国国家自然科学基金;
关键词
axonal regeneration; compressed spinal cord injury; demyelination; electroacupuncture; Schwann cell transplantation; REACTIVE ASTROCYTES; REPAIR; NEUREGULIN-1; INHIBITION; RECOVERY; PROLIFERATION; DEMYELINATION; INFLAMMATION; NEUROTROPHIN; TRANSECTION;
D O I
10.1002/ar.24721
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Axonal impairment and demyelination after compressed spinal cord injury lead to serious neurological dysfunction. Increasing studies have suggested that Schwann cells (SCs) transplantation is a reliable, effective, and promising method for treating spinal cord injury. However, single SCs transplantation is insufficient to promote the full recovery of neurological function. Additional approaches are required to support SCs transplantation as a treatment for spinal cord injury. In the study, we investigated whether the combination of electroacupuncture (EA) and SCs transplantation was a reliable intervention for spinal cord injury. We found that rats in the combination group had significantly higher functional locomotor scores than those received single treatment. By immunostaining, we found EA can not only improve survival and proliferation of transplanted SCs but also inhibit SC apoptosis and block the formation of an astrocytic scar. Additionally, EA promoted regenerated axons extending "bullet-shaped" growth cones into the lesion. Remarkably, EA can modify astrogliosis to promote axonal regeneration following SCs transplantation through inducing extension of astrocytic processes in the SCs graft interface. More importantly, the combination of SCs engraftment and EA can enhance corticospinal-tract axonal regeneration and remyelination after spinal cord injury through up-regulating neuregulin 1 type III in SCs and its downstream signaling mediators. Thus, it is concluded that SCs effectively promote axonal recovery after spinal cord injury when combined with EA stimulation. The experimental results have reinforced the theoretical basis of EA for its clinical efficacy in patients with spinal cord injury and merited further investigation for potential clinical application.
引用
收藏
页码:2506 / 2520
页数:15
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