Gildea Holly K, Liddelow Shane A
Institute for Translational Neuroscience, NYU Grossman School of Medicine, New York, USA.
Department of Neuroscience, NYU Grossman School of Medicine, New York, USA.
Mol Neurodegener. 2025 Feb 21;20(1):21. doi: 10.1186/s13024-025-00810-7.
Normal aging alters brain functions and phenotypes. However, it is not well understood how astrocytes are impacted by aging, nor how they contribute to neuronal dysfunction and disease risk as organisms age. Here, we examine the transcriptional, cell biology, and functional differences in astrocytes across normal aging. Astrocytes at baseline are heterogenous, responsive to their environments, and critical regulators of brain microenvironments and neuronal function. With increasing age, astrocytes adopt different immune-related and senescence-associated states, which relate to organelle dysfunction and loss of homeostasis maintenance, both cell autonomously and non-cell autonomously. These perturbed states are increasingly associated with age-related dysfunction and the onset of neurodegeneration, suggesting that astrocyte aging is a compelling target for future manipulation in the prevention of disease.
正常衰老会改变大脑功能和表型。然而,目前人们对星形胶质细胞如何受到衰老影响,以及随着生物体衰老它们如何导致神经元功能障碍和疾病风险了解甚少。在这里,我们研究了正常衰老过程中星形胶质细胞的转录、细胞生物学和功能差异。基线状态下的星形胶质细胞具有异质性,对其环境有反应,并且是脑微环境和神经元功能的关键调节因子。随着年龄的增长,星形胶质细胞呈现出不同的免疫相关和衰老相关状态,这与细胞器功能障碍以及体内平衡维持的丧失有关,无论是在细胞自主还是非细胞自主方面。这些紊乱状态越来越多地与年龄相关的功能障碍和神经退行性变的发生相关,这表明星形胶质细胞衰老可能是未来疾病预防干预的一个有吸引力的靶点。