Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, 1461884513, Iran.
Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mol Biol Rep. 2024 Feb 24;51(1):353. doi: 10.1007/s11033-024-09292-0.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by repetitive behaviors, a limited range of activities, and deficiencies in social communications. Bone marrow mesenchymal stem cells (BM-MSCs), which secrete factors that stimulate surrounding microenvironment, and BM-MSCs conditioned medium (BM-MSCs-CM), which contains cell-secreted products, have been speculated to hold potential as a therapy for ASD. This study aimed to compare the therapeutic effects of BM-MSCs and BM-MSCs-CM on behavioral and microglial changes in an animal model of autism induced by valproic acid (VPA).
Pregnant Wistar rats were administered by VPA at a dose of 600 mg/kg at 12.5 days post-conception. After birth, male pups were included in the study. At 6 weeks of age, one group of rats received intranasal administration of BM-MSCs, while another group received BM-MSCs-CM. The rats were allowed to recover for 2 weeks. Behavioral tests, quantitative real-time polymerase chain reaction (qRT-PCR), and immunohistochemistry were performed. Both BM-MSCs and BM-MSCs-CM administration significantly improved some behavioral deficits. Furthermore, these treatments notably reduced Iba-1 marker associated with microgliosis. Additionally, there was a significant reduction in the expression of pro-inflammatory cytokines IL-1β and IL-6, and an increase in the levels of the anti-inflammatory cytokine IL-10 in rats administered by BM-MSCs and BM-MSCs-CM.
Post-developmental administration of BM-MSCs and BM-MSCs-CM can ameliorate prenatal neurodevelopmental deficits, restore cognitive and social behaviors, and modulate microglial and inflammatory markers. Results indicated that the improvement rate was higher in the BM-MSCs group than BM-MSCs-CM group.
自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是重复行为、活动范围有限以及社交沟通缺陷。骨髓间充质干细胞(BM-MSCs)分泌刺激周围微环境的因子,BM-MSCs 条件培养基(BM-MSCs-CM)含有细胞分泌产物,被认为具有治疗 ASD 的潜力。本研究旨在比较 BM-MSCs 和 BM-MSCs-CM 对丙戊酸(VPA)诱导的自闭症动物模型中行为和小胶质细胞变化的治疗效果。
妊娠 Wistar 大鼠在受孕后 12.5 天给予 VPA 剂量为 600mg/kg。出生后,雄性幼鼠被纳入研究。在 6 周龄时,一组大鼠接受 BM-MSCs 鼻内给药,另一组接受 BM-MSCs-CM。大鼠恢复 2 周后进行行为测试、定量实时聚合酶链反应(qRT-PCR)和免疫组织化学检测。BM-MSCs 和 BM-MSCs-CM 给药均显著改善了一些行为缺陷。此外,这些治疗方法显著减少了与小胶质细胞增生相关的 Iba-1 标志物。此外,BM-MSCs 和 BM-MSCs-CM 给药的大鼠中促炎细胞因子 IL-1β和 IL-6 的表达显著降低,抗炎细胞因子 IL-10 的水平升高。
发育后给予 BM-MSCs 和 BM-MSCs-CM 可改善产前神经发育缺陷,恢复认知和社交行为,并调节小胶质细胞和炎症标志物。结果表明,BM-MSCs 组的改善率高于 BM-MSCs-CM 组。