Astrocyte to neuron reprogramming with NeuroD1 for repair in canine stroke.

IF 1.2
Frontiers in stroke Pub Date : 2025-07-02 eCollection Date: 2025-01-01 DOI:10.3389/fstro.2025.1602076
Isaac H Clark, Zachary Roushdy, Dilmareth Natera-Rodriguez, Kevin Sun, Olivia Erlanson, Shaimaa Khedr, Walter C Low, Andrew W Grande
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Abstract

Stroke affects hundreds of thousands of people each year and leads to neuronal damage and often long term disabilities. This study served as an exploratory study investigating astrocyte to neuron reprogramming as a potential treatment for ischemic stroke using a canine model to assess anatomical and functional recovery. The study's exploratory nature involved a small sample size, precluding statistically significant conclusions. For treatment, an adeno associated viral (AAV) vector was constructed such that it would target astrocytes and allow expression of NeuroD1 for the intent of reprogramming them into neurons. Animals were analyzed anatomically using MRI scanning, behaviorally with neurological severity score testing, and cellularly with immunohistochemistry staining. Behaviorally, treated animals recovered more rapidly and to a greater extent than controls; anatomically, treated animals also showed much less ventricle enlargement post stroke; and on the cellular level, treated animals showed a decreased level of astrocyte and microglial activation. These findings suggest that NeuroD1-mediated astrocyte reprogramming may reduce neuroinflammation and enhance functional recovery in ischemic stroke, warranting further exploration of this therapeutic approach.

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用NeuroD1重编程星形细胞到神经元修复犬脑卒中。
中风每年影响成千上万的人,并导致神经元损伤和长期残疾。本研究是一项探索性研究,研究星形胶质细胞到神经元的重编程作为缺血性中风的潜在治疗方法,使用犬模型来评估解剖和功能恢复。该研究的探索性性质涉及小样本量,排除了统计上显著的结论。为了治疗,构建了腺相关病毒(AAV)载体,使其能够靶向星形胶质细胞,并允许表达NeuroD1,目的是将其重新编程为神经元。用MRI扫描对动物进行解剖分析,用神经严重程度评分测试对动物进行行为分析,并用免疫组织化学染色对动物进行细胞分析。从行为上看,接受治疗的动物比对照组恢复得更快、程度更大;解剖上,治疗过的动物中风后心室增大也明显减少;在细胞水平上,接受治疗的动物的星形胶质细胞和小胶质细胞的激活水平下降。这些发现表明,neurod1介导的星形胶质细胞重编程可能减少缺血性卒中的神经炎症并增强功能恢复,值得进一步探索这种治疗方法。
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