Shirley Thomas L, Lewers J Chris, Egami Kiyoshi, Majumdar Alokes, Kelly Mairead, Ceballos-Picot Irene, Seidman Michael M, Jinnah H A
Department of Neurology, Johns Hopkins University, Baltimore, Maryland, USA, and Department of Biology, Necker-Enfants Malades Hospital, Paris, France.
J Neurochem. 2007 May;101(3):841-53. doi: 10.1111/j.1471-4159.2007.04472.x.
Mutations in the gene encoding the purine salvage enzyme, hypoxanthine-guanine phosphoribosyltransferase (HPRT) cause Lesch-Nyhan disease, a neurodevelopmental disorder characterized by cognitive, neurological, and behavioral abnormalities. Despite detailed knowledge of the enzyme's function, the key pathophysiological changes that accompany loss of purine recycling are unclear. To facilitate delineating the consequences of HPRT deficiency, four independent HPRT-deficient sublines of the human dopaminergic neuroblastoma, SK-N-BE(2) M17, were isolated by targeted mutagenesis with triple helix-forming oligonucleotides. As a group, these HPRT-deficient cells showed several significant abnormalities: (i) impaired purine recycling with accumulation of hypoxanthine, guanine, and xanthine, (ii) reduced guanylate energy charge and GTP:GDP ratio, but normal adenylate energy charge and no changes in any adenine nucleotide ratios, (iii) increased levels of UTP and NADP+, (iv) reduced DOPA decarboxylase, but normal monoamines, and (v) reduction in cell soma size. These cells combine the analytical power of multiple lines and a human, neuronal origin to provide an important tool to investigate the pathophysiology of HPRT deficiency.
编码嘌呤补救酶次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HPRT)的基因突变会导致莱施 - 奈恩病,这是一种神经发育障碍,其特征为认知、神经和行为异常。尽管对该酶的功能有详细了解,但嘌呤再循环丧失所伴随的关键病理生理变化仍不清楚。为了便于阐明HPRT缺乏的后果,通过用三链形成寡核苷酸进行靶向诱变,分离出了人多巴胺能神经母细胞瘤SK - N - BE(2) M17的四个独立的HPRT缺陷亚系。总体而言,这些HPRT缺陷细胞表现出几个显著异常:(i)嘌呤再循环受损,次黄嘌呤、鸟嘌呤和黄嘌呤积累;(ii)鸟苷酸能荷和GTP:GDP比值降低,但腺苷酸能荷正常,且任何腺嘌呤核苷酸比值均无变化;(iii)UTP和NADP+水平升高;(iv)多巴脱羧酶减少,但单胺正常;(v)细胞体大小减小。这些细胞结合了多个细胞系的分析能力以及人类神经元来源,为研究HPRT缺乏的病理生理学提供了一个重要工具。