Osteoclast morphology in autosomal recessive malignant osteopetrosis due to a TCIRG1 gene mutation.

E. Bruder, T. Stallmach, Karin Peier, A. Superti-Furga, P. Vezzoni
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引用次数: 10

Abstract

Bone biopsies were performed before and 7 weeks after transplantation of HLA-compatible bone marrow from the sister of a 3-month-old male infant with malignant autosomal recessive osteopetrosis due to a mutation in the TCIRG1 (ATP6i) gene. The first biopsy showed broad, immature bony trabeculae and no medullary hematopoiesis. Only few osteoclasts were present and electron microscopy showed absence of ruffled borders. The post transplant biopsy revealed donor osteoclasts with ruffled borders and intracytoplasmic mineral crystals as proof of active bone resorption that had not yet been detectable radiographically. Osteopetrosis is a genetically heterogeneous disease. Definition at the DNA-level will enable comparison of treatment strategies and prenatal diagnosis. As shown in this patient, the autosomal recessive form caused by a TCIRG1 gene mutation may be amenable to bone marrow transplantation. Activity of donor osteoclasts can be demonstrated morphologically on biopsy, before bone remodeling becomes evident radiologically.
TCIRG1基因突变引起的常染色体隐性恶性骨质疏松症的破骨细胞形态。
在移植hla相容骨髓前和移植后7周,对一例因TCIRG1 (ATP6i)基因突变而患有恶性常染色体隐性骨质疏松症的3个月大男婴的妹妹进行骨活检。第一次活检显示骨小梁宽,未成熟,无髓质造血。只有少量破骨细胞存在,电镜显示没有褶皱边界。移植后活检显示,供体破骨细胞边界皱褶,胞浆内矿物晶体为骨吸收活跃的证据,而x线摄影尚未检测到。骨质疏松症是一种遗传异质性疾病。在dna水平的定义将使治疗策略和产前诊断的比较。正如本例患者所示,由TCIRG1基因突变引起的常染色体隐性形式可能适合骨髓移植。供体破骨细胞的活性可以在活检形态学上证实,在骨重塑影像学上变得明显之前。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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