胎母微嵌合和遗传诊断:关于孕妇胎儿细胞和无细胞胎儿DNA的起源

IF 6.4 2区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Margit Rosner , Thomas Kolbe , Markus Hengstschläger
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引用次数: 5

摘要

在怀孕期间,几种类型的胎儿细胞和胎儿干细胞,包括妊娠相关祖细胞(妊娠相关祖细胞),进入母体循环。尽管它们也迁移到母体的各个器官,并采用目标组织的表型来促进再生过程,但胎儿细胞也在母体疾病的发病机制中发挥作用。此外,在孕妇血浆中可检测到无细胞胎儿DNA (cffDNA)。它们共同构成了众所周知的胎母微嵌合现象,激发了使用母体血液进行无创产前检测(NIPT)的概念。深入了解这些胎儿细胞和cffDNA的起源,可以更全面地了解胎母微嵌合的生物学相关性,并对临床应用的持续扩展产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetomaternal microchimerism and genetic diagnosis: On the origins of fetal cells and cell-free fetal DNA in the pregnant woman

During pregnancy several types of fetal cells and fetal stem cells, including pregnancy-associated progenitor cells (PAPCs), traffic into the maternal circulation. Whereas they also migrate to various maternal organs and adopt the phenotype of the target tissues to contribute to regenerative processes, fetal cells also play a role in the pathogenesis of maternal diseases. In addition, cell-free fetal DNA (cffDNA) is detectable in the plasma of pregnant women. Together they constitute the well-known phenomenon of fetomaternal microchimerism, which inspired the concept of non-invasive prenatal testing (NIPT) using maternal blood. An in-depth knowledge concerning the origins of these fetal cells and cffDNA allows a more comprehensive understanding of the biological relevance of fetomaternal microchimerism and has implications for the ongoing expansion of resultant clinical applications.

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来源期刊
CiteScore
12.20
自引率
1.90%
发文量
22
审稿时长
15.7 weeks
期刊介绍: The subject areas of Reviews in Mutation Research encompass the entire spectrum of the science of mutation research and its applications, with particular emphasis on the relationship between mutation and disease. Thus this section will cover advances in human genome research (including evolving technologies for mutation detection and functional genomics) with applications in clinical genetics, gene therapy and health risk assessment for environmental agents of concern.
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