Dendritic Spine Density and Dynamics of Layer 5 Pyramidal Neurons of the Primary Motor Cortex Are Elevated With Aging

被引:16
作者
Davidson, A. M. [1 ,3 ]
Mejia-Gomez, H. [2 ,3 ]
Jacobowitz, M. [3 ]
Mostany, R. [3 ,4 ]
机构
[1] Tulane Univ, Dept Cell & Mol Biol, New Orleans, LA 70118 USA
[2] Tulane Univ, Brain Inst, Neurosci Program, New Orleans, LA 70118 USA
[3] Tulane Univ, Sch Med, Dept Pharmacol, 1430 Tulane Ave,Mail Code 8683, New Orleans, LA 70112 USA
[4] Tulane Univ, Brain Inst, New Orleans, LA 70118 USA
基金
美国国家卫生研究院;
关键词
apical dendrite; cognitive impairment; in vivo imaging; spine clustering; structural plasticity; LONG-TERM; PREFRONTAL CORTEX; VISUAL-CORTEX; MICE; MONKEY; ORGANIZATION; PLASTICITY; STABILITY; MEMORY; MORPHOLOGY;
D O I
10.1093/cercor/bhz124
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is well established that motor impairment often occurs alongside healthy aging, leading to problems with fine motor skills and coordination. Although previously thought to be caused by neuronal death accumulating across the lifespan, it is now believed that the source of this impairment instead stems from more subtle changes in neural connectivity. The dendritic spine is a prime target for exploration of this problem because it is the postsynaptic partner of most excitatory synapses received by the pyramidal neuron, a cortical cell that carries much of the information processing load in the cerebral cortex. We repeatedly imaged the same dendrites in young adult and aged mouse motor cortex over the course of 1 month to look for differences in the baseline state of the dendritic spine population. These experiments reveal increased dendritic spine density, without obvious changes in spine clustering, occurring at the aged dendrite. Additionally, aged dendrites exhibit elevated spine turnover and stabilization alongside decreased long-term spine survival. These results suggest that at baseline the aged motor cortex may exist in a perpetual state of relative instability and attempts at compensation. This phenotype of aging may provide clues for future targets of aging-related motor impairment remediation.
引用
收藏
页码:767 / 777
页数:11
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