Department of Neuroscience, Mayo Clinic Florida, Jacksonville, Florida, USA.
Nat Genet. 2011 Dec 25;44(2):200-5. doi: 10.1038/ng.1027.
Hereditary diffuse leukoencephalopathy with spheroids (HDLS) is an autosomal-dominant central nervous system white-matter disease with variable clinical presentations, including personality and behavioral changes, dementia, depression, parkinsonism, seizures and other phenotypes. We combined genome-wide linkage analysis with exome sequencing and identified 14 different mutations affecting the tyrosine kinase domain of the colony stimulating factor 1 receptor (encoded by CSF1R) in 14 families with HDLS. In one kindred, we confirmed the de novo occurrence of the mutation. Follow-up sequencing identified an additional CSF1R mutation in an individual diagnosed with corticobasal syndrome. In vitro, CSF-1 stimulation resulted in rapid autophosphorylation of selected tyrosine residues in the kinase domain of wild-type but not mutant CSF1R, suggesting that HDLS may result from partial loss of CSF1R function. As CSF1R is a crucial mediator of microglial proliferation and differentiation in the brain, our findings suggest an important role for microglial dysfunction in HDLS pathogenesis.
遗传性弥漫性脑白质病伴轴索性球体(HDLS)是一种常染色体显性遗传的中枢神经系统白质疾病,具有多种临床表现,包括人格和行为改变、痴呆、抑郁、帕金森病、癫痫发作和其他表型。我们结合全基因组连锁分析和外显子组测序,在 14 个 HDLS 家系中发现了 14 种不同的突变,这些突变影响集落刺激因子 1 受体(CSF1R 编码)的酪氨酸激酶结构域。在一个家族中,我们证实了该突变的新生发生。后续测序在被诊断为皮质基底节综合征的个体中鉴定出另一个 CSF1R 突变。体外研究表明,CSF-1 刺激导致野生型 CSF1R 激酶结构域中某些酪氨酸残基的快速自身磷酸化,但突变型 CSF1R 则不然,这表明 HDLS 可能是 CSF1R 部分功能丧失的结果。由于 CSF1R 是大脑中小胶质细胞增殖和分化的关键介质,我们的研究结果表明微胶质功能障碍在 HDLS 发病机制中起重要作用。