| Literature DB >> 26232646 |
Ruiyan Niu1, Xingchen Xue1, Yuhong Zhao2, Zilong Sun1, Xiaoyan Yan3, Xuying Li1, Cuiping Feng4, Jundong Wang5.
Abstract
Axonal and dendrictic degenerations were observed in non-skeleton fluorosis as the neurological manifestations. Microtubules, composed of the assembled tubulin dimers, are the essential cytoskeleton of axon and dendron. However, the effect of fluoride (F) on microtubules status and tubulin dimer expression in central nerves system remains largely unknown. In this study, the ultrastructure of microtubules and expression of Tubα1a and Tubβ2a were detected in hippocampus of mice orally administrated with 25, 50, or 100mgL(-1) NaF for 60d. Results showed that in F treatment groups, microtubules were broken into discrete fragments and bended, which were no longer stretched and went along the axon well. In addition, the expression of Tubα1a and Tubβ2a on both gene and protein levels were significantly reduced in high F group. The visual results of immunocytochemistry also confirmed the decreased protein expressions of Tubα1a and Tubβ2a. These findings suggested that microtubule lesions could be an important cause for neurodegeneration observed in fluorosis, and F may threaten the microtubule stability by affecting the expression of tubulin dimers.Entities:
Keywords: Fluoride; Hippocampus; Microtubule; Tubα1a; Tubβ2a
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Year: 2015 PMID: 26232646 DOI: 10.1016/j.chemosphere.2015.07.011
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086