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

IF 4.4 4区 医学 Q2 CELL & TISSUE ENGINEERING
Won Sun Lee, Soon Jin Choi, Young Ho Shin, Jae Kwang Kim
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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.

表达杆状病毒工程脑源性神经营养因子的间充质干细胞促进大鼠周围神经再生模型。
背景:周围神经损伤由于其复杂的性质和有限的再生能力是一个主要的临床挑战。本研究旨在利用华顿水母间充质干细胞(WJ-MSCs)通过杆状病毒(BV)载体表达脑源性神经营养因子(BDNF),促进周围神经再生。在大鼠坐骨神经缺损模型中,将这些细胞植入无细胞神经移植物(ANGs),评估其疗效。方法:用重组BV转染WJ-MSCs,上调BDNF的表达。利用这些细胞的条件培养基(CM)处理雪旺细胞(SCs),并评估其对髓鞘相关标志物的影响,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),以及对哺乳动物雷帕霉素(mTOR)/蛋白激酶B (AKT)/p38信号通路的激活。在体内,将表达bdnf的WJ-MSCs植入ANGs并植入大鼠坐骨神经缺损模型。通过视频步态分析、等距强直力测量、肌肉重量评估、踝关节挛缩角度测量和甲苯胺蓝染色组织学分析来评估功能恢复情况。结果:转染WJ-MSCs后,BDNF表达显著上调。BDNF-MSC CM显著促进SCs中髓鞘形成标志物的表达,激活mTOR/AKT/p38信号通路。在大鼠模型中,与对照组相比,用表达bdnf的WJ-MSCs植入ANGs可改善功能结果,包括脚趾脱落角度增强,等长张力增加,肌肉重量恢复更大,髓鞘轴突总数更多。结论:表达BDNF的WJ-MSCs与ANGs联合使用可显著促进周围神经再生。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tissue engineering and regenerative medicine
Tissue engineering and regenerative medicine CELL & TISSUE ENGINEERING-ENGINEERING, BIOMEDICAL
CiteScore
6.80
自引率
5.60%
发文量
83
审稿时长
6-12 weeks
期刊介绍: Tissue Engineering and Regenerative Medicine (Tissue Eng Regen Med, TERM), the official journal of the Korean Tissue Engineering and Regenerative Medicine Society, is a publication dedicated to providing research- based solutions to issues related to human diseases. This journal publishes articles that report substantial information and original findings on tissue engineering, medical biomaterials, cells therapy, stem cell biology and regenerative medicine.
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