Santana Nelyane N M, da Silva Maria M O, Silva Eryck H A, Dos Santos Sâmarah F, Bezerra Lyzandro L F, Escarião Wellydo K M, Vasiljevic Gabriel A M, Fiuza Felipe P, Cavalcante Jeferson S, Engelberth Rovena Clara
Department of Physiology and Behavior, Laboratory of Neurochemical Studies, Bioscience Center, Federal University of Rio Grande do Norte, Natal, Brazil.
Edmond and Lily Safra International Institute of Neuroscience, Santos Dumont Institute, Macaíba, Brazil.
PLoS One. 2025 May 23;20(5):e0323906. doi: 10.1371/journal.pone.0323906. eCollection 2025.
Compelling evidence links age-related brain dysfunction and neurodegenerative processes to persistent disruptions in intracellular calcium (Ca2+) signaling, a central hypothesis in the Ca2+ theory of aging. Calbindin (CB), a classical Ca2+ buffer, has been implicated in region-specific susceptibility to aging-related effects. Specifically, CB-immunopositive (CB+) neurons have demonstrated an age-dependent decline in neuronal number across various cortical and subcortical regions. However, it remains unclear whether this decrease occur in the dorsal lateral geniculate nucleus (DLG), a crucial relay and modulatory center for visual processing. Additionally, the potential impact of aging on the cellular volume of CB+ neurons in the DLG has not been fully elucidated, albeit an age-dependent neuronal hypertrophy of this region has been reported. To address these questions, we investigated CB+ neurons in the DLG of six marmosets (Callithrix jacchus), aged between 29-143 months. Using design-based stereological techniques, we estimated the total number and somal volume of CB+ neurons in DLG layers. Our results revealed no signs of CB+ neuronal number loss and somal volumetric changes in aged DLG, particularly within the koniocellular layers, a stratum that primarily expresses CB and play a critical role in blue/yellow color vision. Altogether, our findings suggest a preserved neuronal number and cellular volume of the CB+ population during aging process in the marmoset DLG. Moreover, they provide a valuable basis for future investigations into the neuroprotective role of CB in visual processing during aging and open avenues for strategies designed to preserve vulnerable neuronal populations in age-related neurodegenerative conditions.
确凿的证据将与年龄相关的脑功能障碍和神经退行性过程与细胞内钙(Ca2+)信号的持续紊乱联系起来,这是衰老的Ca2+理论中的一个核心假设。钙结合蛋白(CB)是一种经典的Ca2+缓冲蛋白,与衰老相关效应的区域特异性易感性有关。具体而言,CB免疫阳性(CB+)神经元在各个皮质和皮质下区域均表现出神经元数量的年龄依赖性下降。然而,目前尚不清楚这种减少是否发生在背侧外侧膝状核(DLG),这是视觉处理的一个关键中继和调节中心。此外,尽管有报道称该区域存在年龄依赖性神经元肥大,但衰老对DLG中CB+神经元细胞体积的潜在影响尚未完全阐明。为了解决这些问题,我们研究了6只年龄在29至143个月之间的狨猴(Callithrix jacchus)DLG中的CB+神经元。使用基于设计的体视学技术,我们估计了DLG各层中CB+神经元的总数和体细胞体积。我们的结果显示,在老年DLG中,尤其是在主要表达CB并在蓝/黄颜色视觉中起关键作用的小细胞层内,没有CB+神经元数量减少和体细胞体积变化的迹象。总之,我们的研究结果表明,在狨猴DLG的衰老过程中,CB+群体的神经元数量和细胞体积得以保留。此外,它们为未来研究CB在衰老过程中的视觉处理中的神经保护作用提供了有价值的基础,并为旨在保护与年龄相关的神经退行性疾病中易损神经元群体的策略开辟了道路。