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HMGA2 的表达失调与阵发性睡眠性血红蛋白尿症中 PIGA 缺陷细胞的克隆扩增有关。

Deregulated expression of HMGA2 is implicated in clonal expansion of PIGA deficient cells in paroxysmal nocturnal haemoglobinuria.

机构信息

Department of Immunoregulation, Research Institute for Microbial Diseases Department of Immunoglycobiology, WPI Immunology Frontier Research Centre, Osaka, Japan.

出版信息

Br J Haematol. 2012 Feb;156(3):383-7. doi: 10.1111/j.1365-2141.2011.08914.x. Epub 2011 Oct 24.

Abstract

Patients with paroxysmal nocturnal haemoglobinuria (PNH) have expanded clonal cells bearing a somatic mutation in the PIGA gene. Our previous study on two PNH patients with chromosome 12 rearrangements demonstrated the involvement of HMGA2 expression in clonal expansion. The present study investigated HMGA2 expression in PNH patients without chromosomal abnormalities. The expression of short HMGA2 with latent exon was significantly high in peripheral blood cells from 18 of 24 patients. Over-expression of truncated HMGA2 in mouse bone marrow cells caused expansion in recipient mice. These results support the idea that deregulated expression of HMGA2 causes expansion of PNH cells.

摘要

阵发性睡眠性血红蛋白尿症(PNH)患者具有携带 PIGA 基因突变的克隆性扩展细胞。我们之前对 2 例存在 12 号染色体重排的 PNH 患者的研究表明,HMGA2 表达参与了克隆性扩展。本研究调查了无染色体异常的 PNH 患者中 HMGA2 的表达情况。在 24 例患者中的 18 例外周血细胞中,短 HMGA2 与潜伏外显子的表达显著升高。截断的 HMGA2 在小鼠骨髓细胞中的过表达导致受者小鼠的扩增。这些结果支持 HMGA2 表达失调导致 PNH 细胞扩增的观点。

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