Department of Biological Sciences, Southern Methodist University, Dallas, TX 75275, USA.
Exp Biol Med (Maywood). 2018 Apr;243(7):627-638. doi: 10.1177/1535370218761149. Epub 2018 Feb 27.
A defining feature of neurodegenerative diseases is the abnormal and excessive loss of neurons. One molecule that is particularly important in promoting neuronal death in a variety of cell culture and in vivo models of neurodegeneration is histone deacetylase-3 (HDAC3), a member of the histone deacetylase family of proteins. As a step towards understanding how HDAC3 promotes neuronal death, we conducted a proteomic screen aimed at identifying proteins that were regulated by HDAC3. HDAC3 was overexpressed in cultured rat cerebellar granule neurons (CGNs) and protein lysates were analyzed by mass spectrometry. Of over 3000 proteins identified in the screen, only 21 proteins displayed a significant alteration in expression. Of these, 12 proteins were downregulated whereas 9 proteins were upregulated. The altered expression of five of these proteins, TEX10, NPTX1, TFG, TSC1, and NFL, along with another protein that was downregulated in the proteomic screen, HIP1R, was confirmed using Western blots and commercially available antibodies. Because antibodies were not available for some of the proteins and since HDAC3 is a transcriptional regulator of gene expression, we conducted RT-PCR analysis to confirm expression changes. In separate analyses, we also included other proteins that are known to regulate neurodegeneration, including HDAC9, HSF1, huntingtin, GAPDH, FUS, and p65/RELA. Based on our proteomic screen and candidate protein approach, we identify three genes, Nptx1, Hip1r, and Hdac9, all known to regulate neurodegeneration that are robustly regulated by HDAC3. Given their suggested roles in regulating neuronal death, these genes are likely to be involved in regulating HDAC3-mediated neurotoxicity. Impact statement Neurodegenerative diseases are a major medical, social, and economic problem. Recent studies by several laboratories have indicated that histone deacetylase-3 (HDAC3) plays a key role in promoting neuronal death. But the downstream mediators of HDAC3 neurotoxicity have yet to be identified. We conducted a proteomic screen to identify HDAC3 targets the results of which have been described in this report. Briefly, we identify Nptx1, Hip1r, and Hdac9 as genes whose expression is altered by HDAC3. Investigating how these genes are involved in HDAC3 neurotoxicity could shed valuable insight into neurodegenerative disease and identify molecules that can be targeted to treat these devastating disorders.
神经退行性疾病的一个定义特征是神经元的异常和过度丧失。在各种细胞培养和神经退行性变的体内模型中,促进神经元死亡的一种特别重要的分子是组蛋白去乙酰化酶-3(HDAC3),它是组蛋白去乙酰化酶家族蛋白的成员。为了深入了解 HDAC3 如何促进神经元死亡,我们进行了蛋白质组学筛选,旨在鉴定受 HDAC3 调节的蛋白质。在培养的大鼠小脑颗粒神经元(CGN)中过表达 HDAC3,并通过质谱分析法分析蛋白质裂解物。在筛选出的 3000 多种蛋白质中,只有 21 种蛋白质的表达发生了显著变化。其中,12 种蛋白质下调,9 种蛋白质上调。使用 Western blot 和市售抗体证实了其中 5 种蛋白质(TEX10、NPTX1、TFG、TSC1 和 NFL)以及蛋白质组学筛选中下调的另一种蛋白质 HIP1R 的改变表达。由于一些蛋白质没有可用的抗体,并且由于 HDAC3 是基因表达的转录调节剂,我们进行了 RT-PCR 分析以确认表达变化。在单独的分析中,我们还包括了其他已知调节神经退行性变的蛋白质,包括 HDAC9、HSF1、亨廷顿蛋白、GAPDH、FUS 和 p65/RELA。基于我们的蛋白质组学筛选和候选蛋白质方法,我们确定了三个基因,即 Nptx1、Hip1r 和 Hdac9,它们都已知调节神经退行性变,并且受到 HDAC3 的强烈调节。鉴于它们在调节神经元死亡中的作用,这些基因可能参与调节 HDAC3 介导的神经毒性。影响说明神经退行性疾病是一个主要的医学、社会和经济问题。最近几家实验室的研究表明,组蛋白去乙酰化酶-3(HDAC3)在促进神经元死亡中起着关键作用。但是,HDAC3 神经毒性的下游介质尚未确定。我们进行了蛋白质组学筛选以鉴定 HDAC3 的靶标,本报告中描述了筛选结果。简而言之,我们确定 Nptx1、Hip1r 和 Hdac9 是 HDAC3 表达改变的基因。研究这些基因如何参与 HDAC3 神经毒性可以为神经退行性疾病提供有价值的见解,并确定可以靶向治疗这些毁灭性疾病的分子。