Heidari M, Johnstone D M, Bassett B, Graham R M, Chua A C G, House M J, Collingwood J F, Bettencourt C, Houlden H, Ryten M, Olynyk J K, Trinder D, Milward E A
School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia.
Bosch Institute and Discipline of Physiology, University of Sydney, Sydney, NSW, Australia.
Mol Psychiatry. 2016 Nov;21(11):1599-1607. doi: 10.1038/mp.2015.192. Epub 2016 Jan 5.
The 'neurodegeneration with brain iron accumulation' (NBIA) disease family entails movement or cognitive impairment, often with psychiatric features. To understand how iron loading affects the brain, we studied mice with disruption of two iron regulatory genes, hemochromatosis (Hfe) and transferrin receptor 2 (Tfr2). Inductively coupled plasma atomic emission spectroscopy demonstrated increased iron in the Hfe × Tfr2 brain (P=0.002, n ≥5/group), primarily localized by Perls' staining to myelinated structures. Western immunoblotting showed increases of the iron storage protein ferritin light polypeptide and microarray and real-time reverse transcription-PCR revealed decreased transcript levels (P<0.04, n ≥5/group) for five other NBIA genes, phospholipase A2 group VI, fatty acid 2-hydroxylase, ceruloplasmin, chromosome 19 open reading frame 12 and ATPase type 13A2. Apart from the ferroxidase ceruloplasmin, all are involved in myelin homeostasis; 16 other myelin-related genes also showed reduced expression (P<0.05), although gross myelin structure and integrity appear unaffected (P>0.05). Overlap (P<0.0001) of differentially expressed genes in Hfe × Tfr2 brain with human gene co-expression networks suggests iron loading influences expression of NBIA-related and myelin-related genes co-expressed in normal human basal ganglia. There was overlap (P<0.0001) of genes differentially expressed in Hfe × Tfr2 brain and post-mortem NBIA basal ganglia. Hfe × Tfr2 mice were hyperactive (P<0.0112) without apparent cognitive impairment by IntelliCage testing (P>0.05). These results implicate myelin-related systems involved in NBIA neuropathogenesis in early responses to iron loading. This may contribute to behavioral symptoms in NBIA and hemochromatosis and is relevant to patients with abnormal iron status and psychiatric disorders involving myelin abnormalities or resistant to conventional treatments.
“脑铁沉积神经退行性疾病”(NBIA)家族会导致运动或认知障碍,常伴有精神症状。为了解铁负荷如何影响大脑,我们研究了两种铁调节基因(血色素沉着症基因(Hfe)和转铁蛋白受体2基因(Tfr2))缺失的小鼠。电感耦合等离子体原子发射光谱法显示,Hfe×Tfr2小鼠大脑中的铁含量增加(P = 0.002,每组n≥5),通过普鲁士蓝染色主要定位于髓鞘结构。蛋白质免疫印迹法显示铁储存蛋白铁蛋白轻链多肽增加,基因芯片和实时逆转录聚合酶链反应显示其他五个NBIA相关基因(磷脂酶A2第VI组、脂肪酸2 - 羟化酶、铜蓝蛋白、19号染色体开放阅读框12和ATP酶13A2型)的转录水平降低(P<0.04,每组n≥5)。除了铁氧化酶铜蓝蛋白外,所有这些基因都参与髓鞘稳态;其他16个与髓鞘相关的基因也显示表达降低(P<0.05),尽管总体髓鞘结构和完整性似乎未受影响(P>0.05)。Hfe×Tfr2小鼠大脑中差异表达基因与人类基因共表达网络的重叠(P<0.0001)表明,铁负荷会影响在正常人类基底神经节中共表达的NBIA相关基因和髓鞘相关基因的表达。Hfe×Tfr2小鼠大脑中差异表达的基因与死后NBIA基底神经节中的基因存在重叠(P<0.0001)。通过智能笼测试,Hfe×Tfr2小鼠表现为多动(P<0.0112),但无明显认知障碍(P>0.05)。这些结果表明,在对铁负荷的早期反应中,与髓鞘相关的系统参与了NBIA神经发病机制。这可能导致NBIA和血色素沉着症的行为症状,并且与铁状态异常以及涉及髓鞘异常或对传统治疗耐药的精神疾病患者相关。