School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China; Jiuzhitang Maker (Beijing) Cell Technology Co., LTD., Beijing 102600, China.
Jiuzhitang Maker (Beijing) Cell Technology Co., LTD., Beijing 102600, China.
Life Sci. 2024 Jan 1;336:122330. doi: 10.1016/j.lfs.2023.122330. Epub 2023 Dec 6.
It is recognized that autism spectrum disorder (ASD) is a highly complex neurodevelopmental disorder with communication deficits as well as multiple social barriers. The core symptoms of ASD are not treatable with current therapeutics. Therefore, finding new treatment strategies for ASD is urgently needed. Mesenchymal stem cells (MSC) have been shown to be a promising therapeutic approach in previous studies. However, the underlying mechanisms of MSC treatment for ASD through gut microbiota remain unclear and require further investigation.
BTBR mice were used as ASD model and then randomly assigned to the human bone marrow-derived mesenchymal stem cell (hBMMSC) intravenous treatment group or vehicle treatment group. C57BL/6J (C57) mice served as control. Multiple social behavioral tests were performed during the 6-week period and fecal samples were collected at different time points for 16 s rRNA sequencing analysis.
The administration of hBMMSC improved social deficits of BTBR mice in the open field test (OFT), light-dark box test (LBT), novel object recognition (NOR), and free social test (FST), while also significantly reducing stereotypic behaviors. Additionally, hBMMSC administration notably reversed the alterations of microbiota abundance in BTBR mice, particularly the Firmicutes/Bacteroidetes ratio. Several specific differential taxa were further selected and showed a correlation with the prognosis and behavioral scores of ASD.
Overall, intravenous treatment with hBMMSC had a beneficial impact on ASD by ameliorating social deficits and modifying microbiota compositions. This outcome indicates that hBMMSC intravenous transplantation could be a promising therapeutic strategy for enhancing ASD symptoms improvements.
自闭症谱系障碍(ASD)是一种高度复杂的神经发育障碍,存在沟通缺陷和多种社交障碍。ASD 的核心症状目前无法通过治疗来改善。因此,迫切需要寻找 ASD 的新治疗策略。间充质干细胞(MSC)在先前的研究中已被证明是一种很有前途的治疗方法。然而,MSC 治疗 ASD 对肠道微生物群的潜在机制尚不清楚,需要进一步研究。
BTBR 小鼠被用作 ASD 模型,然后随机分为人骨髓源性间充质干细胞(hBMMSC)静脉治疗组或载体治疗组。C57BL/6J(C57)小鼠作为对照。在 6 周的时间内进行了多种社交行为测试,并在不同时间点收集粪便样本进行 16s rRNA 测序分析。
hBMMSC 的给药改善了 BTBR 小鼠在开阔场测试(OFT)、明暗箱测试(LBT)、新物体识别(NOR)和自由社交测试(FST)中的社交缺陷,同时显著减少刻板行为。此外,hBMMSC 给药明显逆转了 BTBR 小鼠微生物群丰度的改变,特别是厚壁菌门/拟杆菌门的比例。进一步选择了几个特定的差异分类群,这些分类群与 ASD 的预后和行为评分相关。
总体而言,hBMMSC 的静脉给药通过改善社交缺陷和改变微生物群落组成,对 ASD 产生了有益的影响。这一结果表明,hBMMSC 静脉移植可能是一种有前途的治疗策略,可增强 ASD 症状的改善。