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膜型 1 基质金属蛋白酶,MT1-MMP 的突变导致多发性溶骨性骨病和关节炎病温彻斯特综合征。

Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome.

机构信息

Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, NY, USA.

出版信息

Am J Hum Genet. 2012 Sep 7;91(3):572-6. doi: 10.1016/j.ajhg.2012.07.022. Epub 2012 Aug 23.

DOI:10.1016/j.ajhg.2012.07.022
PMID:22922033
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3512002/
Abstract

The "vanishing bone" syndromes represent a group of rare skeletal disorders characterized by osteolysis and joint destruction, which can mimic severe rheumatoid arthritis. Winchester syndrome was one of the first recognized autosomal-recessive, multicentric forms of the disorder. It was originally described nearly 50 years ago in two sisters with a severe crippling osteolysis. Using cultured fibroblasts from the proband, we have now identified homozygous mutations in membrane type-1 metalloproteinase (MT1-MMP or MMP14). We demonstrate that the resulting hydrophobic-region signal-peptide substitution (p.Thr17Arg) decreases MT1-MMP membrane localization with consequent impairment of pro-MMP2 activation, and we propose a structure-based mechanism for this effect.

摘要

“消失的骨头”综合征代表了一组罕见的骨骼疾病,其特征是溶骨和关节破坏,可模拟严重的类风湿关节炎。温彻斯特综合征是最早被识别的常染色体隐性、多中心形式的疾病之一。它最初是在近 50 年前在两名患有严重致残性溶骨的姐妹中描述的。使用来自先证者的培养成纤维细胞,我们现在已经鉴定出膜型 1 金属蛋白酶 (MT1-MMP 或 MMP14) 的纯合突变。我们证明,由此产生的疏水区域信号肽取代 (p.Thr17Arg) 会降低 MT1-MMP 的膜定位,从而导致前 MMP2 的激活受损,我们提出了这种作用的基于结构的机制。

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Am J Hum Genet. 2012 Sep 7;91(3):572-6. doi: 10.1016/j.ajhg.2012.07.022. Epub 2012 Aug 23.
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Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome.基质金属蛋白酶2基因(MMP2)的突变会导致多中心性骨质溶解和关节炎综合征。
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