Liu Yao, Atkinson Rachel A K, Fernandez-Martos Carmen M, Kirkcaldie Matthew T K, Cui Hao, Vickers James C, King Anna E
Wicking Dementia Research and Education Centre, Faculty of Health, University of Tasmania, Hobart, Tasmania, Australia.
Department of Medical Biochemistry and Microbiology, Uppsala University, Biomedical Center, Uppsala, Sweden.
Neurobiol Aging. 2015 Feb;36(2):1151-9. doi: 10.1016/j.neurobiolaging.2014.10.001. Epub 2014 Oct 13.
The transactive response DNA-binding protein 43 (TDP-43) has been identified as a neurofilament light (NF-L) messenger RNA (mRNA)-binding protein. Abnormally increased levels of TDP-43 are detected in patients with amyotrophic lateral sclerosis and a downregulation of NF-L mRNA. However, links between NF-L and TDP-43 expressions are unclear. In this study, we investigated whether the deficiency of NF-L protein can result in alterations in TDP-43 localization or protein expression and whether this is altered with aging. There was a significant increase in TDP-43 protein levels in the cortex and lumbar spinal cord in 12-month-old NF-L knockout (NF-L KO) mice, compared with wild-type (WT) C57BL/6 mice. However, there was no difference in either the phosphorylation of TDP-43 between WT and NF-L KO mice or the abnormal mislocalization of TDP-43 to the cytoplasm in NF-L KO animals. Our findings suggest that NF-L protein or mRNA may negatively affect the expression of TDP-43 in the central nervous system. However, altered phosphorylation of TDP-43 may be more highly associated with aging than the levels of TDP-43 expression.
反式激活反应DNA结合蛋白43(TDP-43)已被鉴定为一种神经丝轻链(NF-L)信使核糖核酸(mRNA)结合蛋白。在肌萎缩侧索硬化症患者中检测到TDP-43水平异常升高,且NF-L mRNA下调。然而,NF-L与TDP-43表达之间的联系尚不清楚。在本研究中,我们调查了NF-L蛋白的缺乏是否会导致TDP-43定位或蛋白表达的改变,以及这是否会随衰老而改变。与野生型(WT)C57BL/6小鼠相比,12月龄NF-L基因敲除(NF-L KO)小鼠的皮质和腰脊髓中TDP-43蛋白水平显著升高。然而,WT小鼠和NF-L KO小鼠之间TDP-43的磷酸化水平或NF-L KO动物中TDP-43向细胞质的异常错误定位均无差异。我们的研究结果表明NF-L蛋白或mRNA可能对中枢神经系统中TDP-43的表达产生负面影响。然而,TDP-43磷酸化的改变可能比TDP-43表达水平与衰老的相关性更高。