Suppr超能文献

细胞死亡作为帕利斯特-基利安综合征中组织局限性镶嵌现象的一种可能机制。

Cell death as a possible mechanism for tissue limited mosaicism in Pallister-Killian syndrome.

作者信息

Tang Wozhan, Wenger Sharon L

机构信息

Department of Pathology, West Virginia University, Morgantown, WV 26506-9203, USA.

出版信息

J Assoc Genet Technol. 2005;31(4):168-9.

Abstract

Pallister-Killian syndrome is a chromosomal mosaic syndrome with a normal and an isochromosome 12p cell line, the latter rarely seen in peripheral blood. The isochromosome 12p cell line decreases with serial passages of fibroblasts in vitro and with age of patient in vivo. To evaluate cell death as a possible mechanism for loss of the abnormal cell line, amniocytes from a fetus with Pallister-Killian syndrome were identified as normal or aneuploid using a chromosome 12 alpha-satellite DNA probe by fluorescent in situ hybridization (FISH) and then subsequently stained with Annexin V, which stains the cytoplasm of cells that are dying. Although not conclusive, our preliminary results suggest that the abnormal cell line is going through apoptosis or necrosis at a higher rate than normal cells. Cell death may be a possible mechanism for decrease of the aneuploid cell line in patients with Pallister-Killian syndrome.

摘要

帕利斯特-基利安综合征是一种染色体嵌合综合征,具有正常细胞系和12p等臂染色体细胞系,后者在外周血中罕见。12p等臂染色体细胞系在体外随着成纤维细胞的传代以及在体内随着患者年龄增长而减少。为了评估细胞死亡是否是异常细胞系丢失的一种可能机制,通过荧光原位杂交(FISH)使用12号染色体α卫星DNA探针将一名患有帕利斯特-基利安综合征胎儿的羊膜细胞鉴定为正常或非整倍体,随后用膜联蛋白V染色,膜联蛋白V可对正在死亡的细胞的细胞质进行染色。尽管结果尚无定论,但我们的初步结果表明,异常细胞系正在经历比正常细胞更高比率的凋亡或坏死。细胞死亡可能是帕利斯特-基利安综合征患者非整倍体细胞系减少的一种可能机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验