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表达杆状病毒工程化脑源性神经营养因子的间充质干细胞改善大鼠模型中的周围神经再生

Mesenchymal Stem Cells Expressing Baculovirus-Engineered Brain-Derived Neurotrophic Factor Improve Peripheral Nerve Regeneration in a Rat Model.

作者信息

Lee Won Sun, Choi Soon Jin, Shin Young Ho, Kim Jae Kwang

机构信息

Department of Orthopedic Surgery Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic Road 43-Gil, Songpa-Gu, Seoul, 05505, Republic of Korea.

Asan Institute for Life Sciences, Seoul, Republic of Korea.

出版信息

Tissue Eng Regen Med. 2025 Apr;22(3):351-362. doi: 10.1007/s13770-025-00703-2. Epub 2025 Feb 17.

Abstract

BACKGROUND

Peripheral nerve injuries are a major clinical challenge because of their complex nature and limited regenerative capacity. This study aimed to improve peripheral nerve regeneration using Wharton's jelly mesenchymal stem cells (WJ-MSCs) engineered to express brain-derived neurotrophic factor (BDNF) via a baculovirus (BV) vector. The cells were evaluated for efficacy when seeded into acellular nerve grafts (ANGs) in a rat sciatic nerve defect model.

METHODS

WJ-MSCs were transfected with recombinant BV to upregulate BDNF expression. Conditioned medium (CM) from these cells was utilized to treat Schwann cells (SCs), and the impact on myelination-related markers, including KROX20, myelin basic protein (MBP), glial fibrillary acidic protein (GFAP), and S100 calcium-binding protein β (S100β), and the activation of the mammalian target of rapamycin (mTOR)/ protein kinase B (AKT)/p38 signaling pathways were evaluated. In vivo, BDNF-expressing WJ-MSCs were seeded into ANGs and implanted into a rat sciatic nerve defect model. Functional recovery was evaluated via video gait analysis, isometric tetanic force measurement, muscle weight evaluation, ankle contracture angle measurement, and histological analysis using toluidine blue staining.

RESULTS

BDNF expression was significantly upregulated in WJ-MSCs post-transfection. BDNF-MSC CM substantially promoted the expression of myelination markers in SCs and activated the mTOR/AKT/p38 signaling pathway. In the rat model, seeding of ANGs with BDNF-expressing WJ-MSCs resulted in improved functional outcomes, including enhanced toe-off angles, increased isometric tetanic force, greater muscle weight recovery, and a higher total number of myelinated axons compared with controls.

CONCLUSION

WJ-MSCs engineered to express BDNF significantly enhanced peripheral nerve regeneration when utilized in conjunction with ANGs. These findings indicate BDNF-expressing WJ-MSCs are a promising therapeutic approach for treating peripheral nerve injuries.

摘要

背景

周围神经损伤因其性质复杂且再生能力有限,是一项重大的临床挑战。本研究旨在利用经杆状病毒(BV)载体工程化表达脑源性神经营养因子(BDNF)的沃顿胶间充质干细胞(WJ-MSCs)来促进周围神经再生。在大鼠坐骨神经缺损模型中,将这些细胞接种到脱细胞神经移植物(ANGs)中,评估其疗效。

方法

用重组BV转染WJ-MSCs以上调BDNF表达。利用这些细胞的条件培养基(CM)处理雪旺细胞(SCs),评估其对髓鞘形成相关标志物的影响,包括KROX20、髓鞘碱性蛋白(MBP)、胶质纤维酸性蛋白(GFAP)和S100钙结合蛋白β(S100β),以及对雷帕霉素哺乳动物靶蛋白(mTOR)/蛋白激酶B(AKT)/p38信号通路的激活作用。在体内,将表达BDNF的WJ-MSCs接种到ANGs中,并植入大鼠坐骨神经缺损模型。通过视频步态分析、等长强直力量测量、肌肉重量评估、踝关节挛缩角度测量以及使用甲苯胺蓝染色的组织学分析来评估功能恢复情况。

结果

转染后WJ-MSCs中BDNF表达显著上调。BDNF-MSC CM显著促进了SCs中髓鞘形成标志物的表达,并激活了mTOR/AKT/p38信号通路。在大鼠模型中,与对照组相比,将表达BDNF的WJ-MSCs接种到ANGs中可改善功能结局,包括增强离地角度、增加等长强直力量、更好地恢复肌肉重量以及增加有髓轴突的总数。

结论

经工程化表达BDNF的WJ-MSCs与ANGs联合使用时,可显著增强周围神经再生。这些发现表明,表达BDNF的WJ-MSCs是治疗周围神经损伤的一种有前景的治疗方法。

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