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镰状小鼠的白质异常和认知功能障碍与星形胶质细胞活化有关。

White-matter abnormalities and cognitive dysfunction are linked to astrocyte activation in sickle mice.

作者信息

Hazra Rimi, Pu Hongjian, Foley Lesley M, Little-Ihrig Lynda, Hitchens T Kevin, Ghosh Samit, Ofori-Acquah Solomon F, Hu Xiaoming, Novelli Enrico M

机构信息

Department of Medicine, Pittsburgh Heart Lung and Blood Vascular Medicine Institute, University of Pittsburgh, 200 Lothrop Street, Pittsburgh, PA 15261, USA.

Department of Neurology, University of Pittsburgh, 3471 Fifth Avenue, Pittsburgh, PA 15213, USA.

出版信息

PNAS Nexus. 2023 May 2;2(5):pgad149. doi: 10.1093/pnasnexus/pgad149. eCollection 2023 May.

Abstract

White-matter injury in sickle-cell disease (SCD) includes silent cerebral infarction diagnosed by diffusion tensor imaging (DTI), a complication associated with cognitive dysfunction in children with SCD. The link between white-matter injury and cognitive dysfunction has not been fully elucidated. The goal of this study was to define whether cerebrovascular lesions and cognitive function in SCD are linked to neuroaxonal damage and astrocyte activation in humanized Townes' SCD mice homozygous for human sickle hemoglobin S (SS) and control mice homozygous for human normal hemoglobin A (AA). Mice underwent MRI with DTI and cognitive testing, and histology sections from their brains were stained to assess microstructural tissue damage, neuroaxonal damage, and astrocyte activation. Fractional anisotropy, showing microstructural cerebrovascular abnormalities identified by DTI in the white matter, was significantly associated with neuronal demyelination in the SS mouse brain. SS mice had reduced learning and memory function with a significantly lower discrimination index compared with AA control mice in the novel object recognition tests. Neuroaxonal damage in the SS mice was synchronously correlated with impaired neurocognitive function and activation of astrocytes. The interplay between astrocyte function and neurons may modulate cognitive performance in SCD.

摘要

镰状细胞病(SCD)中的白质损伤包括通过扩散张量成像(DTI)诊断出的无症状脑梗死,这是一种与SCD患儿认知功能障碍相关的并发症。白质损伤与认知功能障碍之间的联系尚未完全阐明。本研究的目的是确定SCD中的脑血管病变和认知功能是否与人类化汤氏SCD小鼠(纯合人类镰状血红蛋白S(SS))和纯合人类正常血红蛋白A(AA)的对照小鼠中的神经轴突损伤和星形胶质细胞活化有关。小鼠接受了带有DTI的MRI检查和认知测试,并对其脑组织切片进行染色,以评估微观结构组织损伤、神经轴突损伤和星形胶质细胞活化。分数各向异性显示了DTI在白质中识别出的微观结构脑血管异常,与SS小鼠脑内的神经元脱髓鞘显著相关。在新物体识别测试中,与AA对照小鼠相比,SS小鼠的学习和记忆功能降低,辨别指数显著更低。SS小鼠的神经轴突损伤与神经认知功能受损和星形胶质细胞活化同步相关。星形胶质细胞功能与神经元之间的相互作用可能会调节SCD中的认知表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83f1/10194090/c27b91807f79/pgad149f1.jpg

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