Ma Lina, Li Yun, Wang Rong
Department of Geriatrics, Xuan Wu Hospital, Capital Medical University, Beijing 100053, China.
Department of Geriatrics, Xuan Wu Hospital, Capital Medical University, Beijing 100053, China.
Clin Chim Acta. 2015 Dec 7;451(Pt B):121-4. doi: 10.1016/j.cca.2015.06.021. Epub 2015 Jun 26.
The kinetics of cytoskeletal networks, with actin as a key factor, play a key role in regulating the morphology and function of dendritic spines. Drebrin is a neuron growth and brain development-related actin-binding protein and is present in 70% of the dendritic spines of excitatory synapses. It regulates the development and formation of dendritic spines and well-developed dendritic spines pave the way for presynaptic elements. Well-developed and mature synapses are prerequisite for maintaining nervous system physiology. Abnormal morphology of dendritic spines and loss of synapses are seen in many neurologic diseases associated with cognitive decline. However, the mechanisms governing these pathologic changes and their correlation with drebrin remain unclear. Exploring the relationship between drebrin and cognitive function may provide insight into the early prevention of cognitive impairment and in the diagnosis and treatment of Alzheimer's disease.
以肌动蛋白为关键因素的细胞骨架网络动力学,在调节树突棘的形态和功能方面发挥着关键作用。Drebrin是一种与神经元生长和大脑发育相关的肌动蛋白结合蛋白,存在于70%的兴奋性突触的树突棘中。它调节树突棘的发育和形成,而发育良好的树突棘为突触前元件铺平了道路。发育良好且成熟的突触是维持神经系统生理功能的先决条件。在许多与认知衰退相关的神经疾病中,都可见树突棘形态异常和突触丧失。然而,控制这些病理变化的机制及其与Drebrin的相关性仍不清楚。探索Drebrin与认知功能之间的关系,可能为认知障碍的早期预防以及阿尔茨海默病的诊断和治疗提供思路。