Thrombospondin-1 modified bone marrow mesenchymal stem cells (BMSCs) promote neurite outgrowth and functional recovery in rats with spinal cord injury

被引:23
|
作者
Pu, Yujie [1 ]
Meng, Ke [1 ]
Gu, Chuanlong [1 ]
Wang, Linlin [1 ]
Zhang, Xiaoming [1 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Basic Med Sci, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
spinal cord injury; bone marrow mesenchymal stem cells (BMSCs); thrombospondin-1 (TSP-1); neurite outgrowth; functional recovery; SYNAPSE FORMATION; TRANSPLANTATION; DELIVERY; BETA; REGENERATION; ASTROCYTES; MODULATION; STRATEGIES; APOPTOSIS; PATHWAY;
D O I
10.18632/oncotarget.22018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stem cell therapies are currently gaining momentum in the treatment of spinal cord injury (SCI). However, unsatisfied intrinsic neurite growth capacity constitutes significant obstacles for injured spinal cord repair and ultimately results in neurological dysfunction. The present study assessed the efficacy of thrombospondin-1 (TSP-1), a neurite outgrowth-promoting molecule, modified bone marrow mesenchymal stem cells (BMSCs) on promoting neurite outgrowth in vitro and in vivo of Oxygen-Glucose Deprivation (OGD) treated motor neurons and SCI rat models. The present results demonstrated that the treatment of BMSCs+ TSP-1 could promote the neurite length, neuronal survival, and functional recovery after SCI. Additionally, TSP-1 could activate transforming growth factor-beta 1 (TGF-beta 1) then induced the smad2 phosphorylation, and expedited the expression of GAP-43 to promote neurite outgrowth. The present study for the first time demonstrated that BMSCs+TSP-1 could promote neurite outgrowth and functional recovery after SCI partly through the TGF-beta 1/p-Samd2 pathway. The study provided a novel encouraging evidence for the potential treatment of BMSCs modification with TSP-1 in patients with SCI.
引用
收藏
页码:96276 / 96289
页数:14
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