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间充质干细胞移植促进BTBR小鼠的神经发生并改善自闭症相关行为。

Mesenchymal Stem Cell Transplantation Promotes Neurogenesis and Ameliorates Autism Related Behaviors in BTBR Mice.

作者信息

Segal-Gavish Hadar, Karvat Golan, Barak Noy, Barzilay Ran, Ganz Javier, Edry Liat, Aharony Israel, Offen Daniel, Kimchi Tali

机构信息

Felsenstein Medical Research Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel- Aviv, Israel.

Department of Neurobiology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Autism Res. 2016 Jan;9(1):17-32. doi: 10.1002/aur.1530. Epub 2015 Aug 10.

Abstract

Autism spectrum disorders (ASD) are characterized by social communication deficits, cognitive rigidity, and repetitive stereotyped behaviors. Mesenchymal stem cells (MSC) have a paracrine regenerative effect, and were speculated to be a potential therapy for ASD. The BTBR inbred mouse strain is a commonly used model of ASD as it demonstrates robust behavioral deficits consistent with the diagnostic criteria for ASD. BTBR mice also exhibit decreased brain-derived neurotrophic factor (BDNF) signaling and reduced hippocampal neurogenesis. In the current study, we evaluated the behavioral and molecular effects of intracerebroventricular MSC transplantation in BTBR mice. Transplantation of MSC resulted in a reduction of stereotypical behaviors, a decrease in cognitive rigidity and an improvement in social behavior. Tissue analysis revealed elevated BDNF protein levels in the hippocampus accompanied by increased hippocampal neurogenesis in the MSC-transplanted mice compared with sham treated mice. This might indicate a possible mechanism underpinning the behavioral improvement. Our study suggests a novel therapeutic approach which may be translatable to ASD patients in the future.

摘要

自闭症谱系障碍(ASD)的特征是社交沟通缺陷、认知僵化和重复刻板行为。间充质干细胞(MSC)具有旁分泌再生作用,被推测为ASD的一种潜在治疗方法。BTBR近交系小鼠是一种常用的ASD模型,因为它表现出与ASD诊断标准一致的明显行为缺陷。BTBR小鼠还表现出脑源性神经营养因子(BDNF)信号传导减少和海马神经发生减少。在本研究中,我们评估了脑室内MSC移植对BTBR小鼠行为和分子的影响。MSC移植导致刻板行为减少、认知僵化降低和社交行为改善。组织分析显示,与假手术处理的小鼠相比,MSC移植小鼠海马中的BDNF蛋白水平升高,同时海马神经发生增加。这可能表明行为改善的一种潜在机制。我们的研究提出了一种新的治疗方法,未来可能适用于ASD患者。

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