Cytoskeletal changes during development and aging in the cortex of neurofilament light protein knockout mice

神经丝 生物 细胞骨架 钙黄绿素 中间灯丝 蛋白质亚单位 基因剔除小鼠 细胞生物学 τ蛋白 内分泌学 内科学 分子生物学 免疫组织化学 免疫学 细胞 受体 生物化学 阿尔茨海默病 基因 疾病 医学
作者
Yao Liu,Jerome Staal,AJ Canty,Matthew Kirkcaldie,Anna E. King,Olivier Bibari,Stanislaw Mitew,Tracey C. Dickson,James C. Vickers
出处
期刊:Journal of comparative neurology [Wiley]
卷期号:521 (8): 1817-1827 被引量:15
标识
DOI:10.1002/cne.23261
摘要

Abstract The neurofilament light (NFL) subunit is considered as an obligate subunit polymer for neuronal intermediate filaments comprising the neurofilament (NF) triplet proteins. We examined cytoskeletal protein levels in the cerebral cortex of NFL knockout (KO) mice at postnatal day 4 (P4), 5 months, and 12 months of age compared with age‐matched wild‐type (WT) mice of a similar genetic background (C57BL/6). The absence of NFL protein resulted in a significant reduction of phosphorylated and dephosphorylated NFs (NF‐P, NF‐DP), the medium NF subunit (NFM), and the intermediate filament α‐internexin (INT) at P4. At 5 months, NF‐DP, NFM, and INT remained significantly lower in knockouts. At 12 months, NF‐P was again significantly decreased, and INT significantly increased, in KOs compared with wild type. In addition, protein levels of class III neuron‐specific β‐tubulin and microtubule‐associated protein 2 were significantly increased in NFL KO mice at P4, 5 months, and 12 months, whereas β‐actin levels were significantly decreased at P4. Immunocytochemical studies demonstrated that NF‐DP accumulated abnormally in the perikarya of cortical neurons by 5 months of age in NFL KO mice. Neurons that lacked NF triplet proteins, such as calretinin‐immunolabeled nonpyramidal cells, showed no alterations in density or cytoarchitectural distribution in NFL KO mice at 5 months relative to WT mice, although calretinin protein levels were decreased significantly after 12 months in NFL KO mice. These findings suggest that a lack of NFL protein alters the expression of cytoskeletal proteins and disrupts other NF subunits, causing intracellular aggregation but not gross structural changes in cortical neurons or cytoarchitecture. The data also indicate that changes in expression of other cytoskeletal proteins may compensate for decreased NFs. J. Comp. Neurol. 521:1817–1827, 2013. © 2012 Wiley Periodicals, Inc.
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