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唐氏综合征中短暂异常骨髓造血的单克隆性质。

Monoclonal nature of transient abnormal myelopoiesis in Down's syndrome.

作者信息

Kurahashi H, Hara J, Yumura-Yagi K, Murayama N, Inoue M, Ishihara S, Tawa A, Okada S, Kawa-Ha K

机构信息

Department of Pediatrics, Osaka University Hospital, Japan.

出版信息

Blood. 1991 Mar 15;77(6):1161-3.

PMID:1672097
Abstract

Neonates with Down's syndrome occasionally show an excess of blasts in their peripheral blood. This disorder spontaneously resolves within several months and is called transient abnormal myelopoiesis (TAM) or transient myeloproliferative disorder. It has been uncertain whether the excess of blasts in TAM is a result of a clonal proliferation or a polyclonal reactive condition. The clonality of cells in females can be examined by analysis of the methylation patterns of the X chromosomes of proliferating cells using restriction fragment length polymorphism (RFLP). Using this strategy, we studied three females with Down's syndrome accompanied by TAM who showed heterozygosity in RFLP of either the hypoxanthine phosphoribosyltransferase or phosphoglycerate kinase gene. Analysis of the methylation patterns of these genes demonstrated a clonal nature for blasts in three patients. Thus, TAM is a clonal proliferative disorder. In addition, lymphocytes with a normal appearance contained in analyzed samples from these patients also showed a monoclonal pattern, suggesting that TAM may be a disorder of multipotent stem cells.

摘要

患有唐氏综合征的新生儿外周血中偶尔会出现大量原始细胞。这种病症会在几个月内自行缓解,被称为暂时性异常骨髓造血(TAM)或暂时性骨髓增殖性疾病。目前尚不确定TAM中原始细胞增多是克隆性增殖还是多克隆反应性状态的结果。女性细胞的克隆性可通过使用限制性片段长度多态性(RFLP)分析增殖细胞X染色体的甲基化模式来检测。运用这一策略,我们研究了三名患有唐氏综合征并伴有TAM的女性,她们在次黄嘌呤磷酸核糖转移酶或磷酸甘油酸激酶基因的RFLP中表现出杂合性。对这些基因甲基化模式的分析表明,三名患者的原始细胞具有克隆性质。因此,TAM是一种克隆性增殖性疾病。此外,这些患者分析样本中外观正常的淋巴细胞也显示出单克隆模式,这表明TAM可能是一种多能干细胞疾病。

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