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年龄相关的肌动蛋白解聚因子 1 通路(LIMK1/SSH1)的性别差异及其与慢性系统性炎症后小鼠 AD 生物标志物的关系。

Age-dependent sex differences in cofilin1 pathway (LIMK1/SSH1) and its association with AD biomarkers after chronic systemic inflammation in mice.

机构信息

Department of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614, USA.

Department of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, Toledo, OH 43614, USA.

出版信息

Neurobiol Aging. 2024 Dec;144:43-55. doi: 10.1016/j.neurobiolaging.2024.09.003. Epub 2024 Sep 7.

Abstract

Chronic systemic inflammation (CSI) results in neuroinflammation and neurodegeneration. Cofilin1 is a stress protein that activates microglia and induces neuroinflammation, but its role in CSI at different aging stages remains unidentified. Therefore, the study aims to identify cofilin1 and its upstream regulators LIMK1 and SSH1 after CSI in young-, middle-, and advanced-aged mice. CSI was induced by injecting the male and female mice with a sub-lethal dose of Lipopolysaccharide weekly for six weeks. The results showed that normal male mice did not show cofilin pathway dysregulation, but a significant dysregulation was observed in CSI advanced-aged mice. In females, cofilin1 dysregulation was observed in healthy and CSI advanced-aged mice, while significant cofilin1 dysregulation was observed in middle-aged mice during CSI. Furthermore, cofilin1 pathway dysregulations correlated with Alzheimer's disease (AD) biomarkers in the brain and saliva, astrocyte activation, synaptic degeneration, neurobehavioral impairments, gut-microbiota abnormalities, and circulatory inflammation. These results provide new insights into cofilin1 sex and age-dependent mechanistic differences that might help identify targets for modulating neuroinflammation and early onset of AD.

摘要

慢性系统性炎症(CSI)导致神经炎症和神经退行性变。丝切蛋白 1 是一种应激蛋白,可激活小胶质细胞并诱导神经炎症,但它在不同衰老阶段 CSI 中的作用仍不清楚。因此,本研究旨在鉴定年轻、中年和老年小鼠 CSI 后丝切蛋白 1 及其上游调节因子 LIMK1 和 SSH1。通过每周给雄性和雌性小鼠注射亚致死剂量的脂多糖来诱导 CSI 持续六周。结果表明,正常雄性小鼠没有表现出丝切蛋白通路失调,但 CSI 老年小鼠明显出现失调。在雌性中,健康和 CSI 老年小鼠中观察到丝切蛋白 1 失调,而 CSI 中年小鼠中观察到明显的丝切蛋白 1 失调。此外,丝切蛋白 1 通路失调与大脑和唾液中的阿尔茨海默病(AD)生物标志物、星形胶质细胞激活、突触退化、神经行为损伤、肠道微生物群异常和循环炎症相关。这些结果提供了新的见解,表明丝切蛋白 1 存在性别和年龄依赖性的机制差异,这可能有助于确定调节神经炎症和 AD 早期发病的靶点。

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