Zhang Jiwei, Brown Elizabeth B, Lloyd Evan, Farhy-Tselnicker Isabella, Keene Alex C
bioRxiv. 2025 Apr 3:2025.04.02.646667. doi: 10.1101/2025.04.02.646667.
Neuronal injury due to trauma or neurodegeneration is a common feature of aging. The clearance of damaged neurons by glia is thought to be critical for maintenance of proper brain function. Sleep loss has been shown to inhibit the motility and function of glia that clear damaged axons while enhancement of sleep promotes clearance of damaged axons. Despite the potential role of glia in maintenance of brain function and protection against neurodegenerative disease, surprisingly little is known about how sleep loss impacts glial function in aged animals. Axotomy of the antennae triggers Wallerian degeneration, where specialized olfactory ensheathing glia engulf damaged neurites. This glial response provides a robust model system to investigate the molecular basis for glial engulfment and neuron-glia communication. Glial engulfment is impaired in aged and sleep-deprived animals, raising the possibility that age-related sleep loss underlies deficits in glial function. To define the relationship between sleep- and age-dependent reductions in glial function, we restored sleep to aged animals and examined the effects on glial clearance of damaged axons. Both pharmacological and genetic induction of sleep restores clearance of damaged neurons in aged flies. Further analysis revealed that sleep restored post-injury induction of the engulfment protein Draper to aged flies, fortifying the notion that loss of sleep contributes to reduced glial-mediated debris clearance in aged animals. To identify age-related changes in the transcriptional response to neuronal injury, we used single-nucleus RNA-seq of the central brains from axotomized young and old flies. We identified broad transcriptional changes within the ensheathing glia of young flies, and the loss of transcriptional induction of autophagy-associated genes. We also identify age-dependent loss of transcriptional induction of 18 transcripts encoding for small and large ribosomal protein subunits following injury in old flies, suggesting dysregulation of ribosomal biogenesis contributes to loss of glial function. Together, these findings demonstrate a functional link between sleep loss, aging and Wallerian degeneration.
创伤或神经退行性变导致的神经元损伤是衰老的一个常见特征。神经胶质细胞清除受损神经元被认为对维持大脑正常功能至关重要。睡眠不足已被证明会抑制清除受损轴突的神经胶质细胞的运动性和功能,而增加睡眠则促进受损轴突的清除。尽管神经胶质细胞在维持大脑功能和预防神经退行性疾病方面具有潜在作用,但令人惊讶的是,关于睡眠不足如何影响老年动物的神经胶质细胞功能,我们知之甚少。触角切断会引发华勒氏变性,即专门的嗅觉鞘神经胶质细胞吞噬受损的神经突。这种神经胶质细胞反应提供了一个强大的模型系统,用于研究神经胶质细胞吞噬和神经元 - 神经胶质细胞通讯的分子基础。在老年和睡眠剥夺的动物中,神经胶质细胞吞噬功能受损,这增加了与年龄相关的睡眠不足是神经胶质细胞功能缺陷基础的可能性。为了确定睡眠和年龄依赖性神经胶质细胞功能降低之间的关系,我们恢复了老年动物的睡眠,并检查了对受损轴突的神经胶质细胞清除的影响。药物诱导和基因诱导睡眠都能恢复老年果蝇中受损神经元的清除。进一步分析表明,睡眠恢复了老年果蝇受伤后吞噬蛋白Draper的诱导表达,强化了睡眠不足导致老年动物中神经胶质细胞介导的碎片清除减少的观点。为了确定对神经元损伤的转录反应中与年龄相关的变化,我们对切断触角的年轻和老年果蝇的中枢脑进行了单核RNA测序。我们在年轻果蝇的鞘神经胶质细胞中发现了广泛的转录变化,以及自噬相关基因转录诱导的丧失。我们还发现老年果蝇受伤后,18个编码小核糖体蛋白亚基和大核糖体蛋白亚基的转录本的转录诱导存在年龄依赖性丧失,这表明核糖体生物合成失调导致神经胶质细胞功能丧失。总之,这些发现证明了睡眠不足、衰老和华勒氏变性之间的功能联系。