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GNAS1基因的突变、基质细胞功能障碍以及非McCune-Albright骨纤维发育不良中的骨软化改变。

Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of bone.

作者信息

Bianco P, Riminucci M, Majolagbe A, Kuznetsov S A, Collins M T, Mankani M H, Corsi A, Bone H G, Wientroub S, Spiegel A M, Fisher L W, Robey P G

机构信息

Dipartimento di Medicina Sperimentale, Università dell'Aquila, Italy.

出版信息

J Bone Miner Res. 2000 Jan;15(1):120-8. doi: 10.1359/jbmr.2000.15.1.120.

Abstract

Activating missense mutations of the GNAS1 gene, encoding the alpha subunit of the stimulatory G protein (Gs), have been identified in patients with the McCune-Albright syndrome (MAS; characterized by polyostotic fibrous dysplasia, café au lait skin pigmentation, and endocrine disorders). Because fibrous dysplasia (FD) of bone also commonly occurs outside of the context of typical MAS, we asked whether the same mutations could be identified routinely in non-MAS FD lesions. We analyzed a series of 8 randomly obtained, consecutive cases of non-MAS FD and identified R201 mutations in the GNAS1 gene in all of them by sequencing cDNA generated by amplification of genomic DNA using a standard primer set and by using a novel, highly sensitive method that uses a protein nucleic acid (PNA) primer to block amplification of the normal allele. Histologic findings were not distinguishable from those observed in MAS-related FD and included subtle changes in cell shape and collagen texture putatively ascribed to excess endogenous cyclic adenosine monophosphate (cAMP). Osteomalacic changes (unmineralized osteoid) were prominent in lesional FD bone. In an in vivo transplantation assay, stromal cells isolated from FD failed to recapitulate a normal ossicle; instead, they generated a miniature replica of fibrous dysplasia. These data provide evidence that occurrence of GNAS1 mutations, previously noted in individual cases of FD, is a common and perhaps constant finding in non-MAS FD. These findings support the view that FD, MAS, and nonskeletal isolated endocrine lesions associated with GNAS1 mutations represent a spectrum of phenotypic expressions (likely reflecting different patterns of somatic mosaicism) of the same basic disorder. We conclude that mechanisms underlying the development of the FD lesions, and hopefully mechanism-targeted therapeutic approaches to be developed, must also be the same in MAS and non-MAS FD.

摘要

在患有McCune - Albright综合征(MAS;其特征为多骨纤维发育不良、咖啡牛奶斑皮肤色素沉着和内分泌紊乱)的患者中,已鉴定出编码刺激性G蛋白(Gs)α亚基的GNAS1基因的激活错义突变。由于骨纤维发育不良(FD)也常见于典型MAS之外的情况,我们询问在非MAS的FD病变中是否能常规鉴定出相同的突变。我们分析了一系列8例随机获取的连续非MAS FD病例,并通过使用标准引物组扩增基因组DNA生成的cDNA测序,以及使用一种新型的、高度灵敏的方法(该方法使用蛋白质核酸(PNA)引物来阻断正常等位基因的扩增),在所有病例中均鉴定出GNAS1基因的R201突变。组织学发现与MAS相关的FD中观察到的无异,包括细胞形状和胶原质地的细微变化,推测归因于内源性环磷酸腺苷(cAMP)过多。病变的FD骨中骨软化改变(未矿化的类骨质)很突出。在一项体内移植试验中,从FD分离的基质细胞未能重现正常小骨;相反,它们产生了纤维发育不良的微型复制品。这些数据证明,先前在个别FD病例中发现的GNAS1突变的发生,在非MAS FD中是一个常见且可能持续存在的发现。这些发现支持这样一种观点,即FD、MAS以及与GNAS1突变相关的非骨骼孤立性内分泌病变代表了同一基本疾病的一系列表型表达(可能反映了体细胞镶嵌的不同模式)。我们得出结论,FD病变发展的潜在机制,以及有望开发的针对机制的治疗方法,在MAS和非MAS FD中也必定相同。

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