衰老降低小鼠背外侧纹状体星形细胞终足钙调蛋白表达并改变自发钙信号。

Sara M Zarate, Taylor E Huntington, Pooneh Bagher, Rahul Srinivasan
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引用次数: 1

摘要

与衰老相关的血脑屏障(BBB)和神经血管单位(NVU)损伤增加了神经变性的风险。在参与血脑屏障和NVU功能的多种细胞中,星形细胞终足的钙信号对于维持血脑屏障和NVU的完整性至关重要。为了评估衰老是否与背外侧纹状体(DLS)星形细胞终足钙信号改变有关,我们在年轻(3-4个月)、中年(12-15个月)和衰老(20-30个月)小鼠的DLS星形细胞中表达了GCaMP6f。与年轻小鼠的终足相比,衰老小鼠的DLS终足显示钙网蛋白表达减少,自发膜相关和线粒体钙信号改变。年轻小鼠需要细胞外和内质网钙源来传递终足信号,而中年和老年小鼠则严重依赖内质网钙。因此,星形细胞终足在整个生命周期中显示出钙缓冲和钙来源的显著变化,这对于理解衰老损害血脑屏障和NVU的机制非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Aging reduces calreticulin expression and alters spontaneous calcium signals in astrocytic endfeet of the mouse dorsolateral striatum.

Aging reduces calreticulin expression and alters spontaneous calcium signals in astrocytic endfeet of the mouse dorsolateral striatum.

Aging-related impairment of the blood brain barrier (BBB) and neurovascular unit (NVU) increases the risk for neurodegeneration. Among various cells that participate in BBB and NVU function, calcium signals in astrocytic endfeet are crucial for maintaining BBB and NVU integrity. To assess if aging is associated with altered calcium signals within astrocytic endfeet of the dorsolateral striatum (DLS), we expressed GCaMP6f in DLS astrocytes of young (3-4 months), middle-aged (12-15 months) and aging (20-30 months) mice. Compared to endfeet in young mice, DLS endfeet in aging mice demonstrated decreased calreticulin expression, and alterations to both spontaneous membrane-associated and mitochondrial calcium signals. While young mice required both extracellular and endoplasmic reticulum calcium sources for endfoot signals, middle-aged and aging mice showed heavy dependence on endoplasmic reticulum calcium. Thus, astrocytic endfeet show significant changes in calcium buffering and sources throughout the lifespan, which is important for understanding mechanisms by which aging impairs the BBB and NVU.

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