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胚胎植入前使用前植入因子可改善唐氏综合征小鼠模型的早期产后神经发生和认知障碍。

Prenatal treatment with preimplantation factor improves early postnatal neurogenesis and cognitive impairments in a mouse model of Down syndrome.

机构信息

Université Paris Cité, BFA, UMR 8251, CNRS, Paris, F-75013, France.

Université Paris-Saclay, UVSQ, INRAE, ENVA, BREED, Jouy-en-Josas, 78350, France.

出版信息

Cell Mol Life Sci. 2024 May 13;81(1):215. doi: 10.1007/s00018-024-05245-9.

Abstract

Down syndrome (DS) is a genetic disease characterized by a supernumerary chromosome 21. Intellectual deficiency (ID) is one of the most prominent features of DS. Central nervous system defects lead to learning disabilities, motor and language delays, and memory impairments. At present, a prenatal treatment for the ID in DS is lacking. Subcutaneous administration of synthetic preimplantation factor (sPIF, a peptide with a range of biological functions) in a model of severe brain damage has shown neuroprotective and anti-inflammatory properties by directly targeting neurons and microglia. Here, we evaluated the effect of PIF administration during gestation and until weaning on Dp(16)1Yey mice (a mouse model of DS). Possible effects at the juvenile stage were assessed using behavioral tests and molecular and histological analyses of the brain. To test the influence of perinatal sPIF treatment at the adult stage, hippocampus-dependent memory was evaluated on postnatal day 90. Dp(16)1Yey pups showed significant behavioral impairment, with impaired neurogenesis, microglial cell activation and a low microglial cell count, and the deregulated expression of genes linked to neuroinflammation and cell cycle regulation. Treatment with sPIF restored early postnatal hippocampal neurogenesis, with beneficial effects on astrocytes, microglia, inflammation, and cell cycle markers. Moreover, treatment with sPIF restored the level of DYRK1A, a protein that is involved in cognitive impairments in DS. In line with the beneficial effects on neurogenesis, perinatal treatment with sPIF was associated with an improvement in working memory in adult Dp(16)1Yey mice. Perinatal treatment with sPIF might be an option for mitigating cognitive impairments in people with DS.

摘要

唐氏综合征(DS)是一种以 21 号染色体多余为特征的遗传性疾病。智力缺陷(ID)是 DS 最显著的特征之一。中枢神经系统缺陷导致学习障碍、运动和语言迟缓以及记忆力减退。目前,DS 患者的 ID 缺乏产前治疗。在严重脑损伤模型中,皮下给予合成着床前因子(sPIF,一种具有多种生物学功能的肽)显示出通过直接靶向神经元和小胶质细胞具有神经保护和抗炎特性。在这里,我们评估了在妊娠期和断奶前给予 PIF 对 Dp(16)1Yey 小鼠(DS 的一种小鼠模型)的影响。使用行为测试和大脑的分子和组织学分析评估了幼年阶段的可能影响。为了测试围产期 sPIF 处理对成年期的影响,在产后第 90 天评估了海马依赖性记忆。Dp(16)1Yey 幼鼠表现出明显的行为障碍,神经发生受损,小胶质细胞活化和小胶质细胞计数低,以及与神经炎症和细胞周期调节相关的基因表达失调。sPIF 治疗恢复了早期产后海马神经发生,对星形胶质细胞、小胶质细胞、炎症和细胞周期标志物具有有益作用。此外,sPIF 治疗恢复了 DYRK1A 的水平,该蛋白参与 DS 认知障碍。与神经发生的有益作用一致,围产期 sPIF 治疗与成年 Dp(16)1Yey 小鼠工作记忆的改善相关。围产期 sPIF 治疗可能是减轻 DS 患者认知障碍的一种选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c850/11090972/2cdbb038884e/18_2024_5245_Fig1_HTML.jpg

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