Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
Integr Biol (Camb). 2010 Oct;2(10):510-6. doi: 10.1039/c0ib00068j. Epub 2010 Sep 20.
Embryonic stem (ES) cells are derived from blastocysts. They can differentiate into the three embryonic germ layers and essentially any type of somatic cells. They therefore hold great potential in tissue regeneration therapy. The ethical issues associated with the use of human embryonic stem cells are resolved by the technical break-through of generating induced pluripotent stem (iPS) cells from various types of somatic cells. However, how ES and iPS cells self-renew and maintain their pluripotency is still largely unknown in spite of the great progress that has been made in the last two decades. Integrative genome-wide approaches, such as the gene expression microarray, chromatin immunoprecipitation based microarray (ChIP-chip) and chromatin immunoprecipitation followed by massive parallel sequencing (ChIP-seq) offer unprecedented opportunities to elucidate the mechanism of the pluripotency, reprogramming and DNA damage response of ES and iPS cells. This frontier article summarizes the fundamental biological questions about ES and iPS cells and reviews the recent advances in ES and iPS cell research using genome-wide technologies. To this end, we offer our perspectives on the future of genome-wide studies on stem cells.
胚胎干细胞(ES 细胞)来源于囊胚。它们可以分化为三个胚胎生殖层,并基本上分化为任何类型的体细胞。因此,它们在组织再生治疗方面具有巨大的潜力。通过从各种类型的体细胞中生成诱导多能干细胞(iPS 细胞)的技术突破,解决了与使用人类胚胎干细胞相关的伦理问题。然而,尽管在过去二十年中取得了巨大的进展,但 ES 和 iPS 细胞如何自我更新并维持其多能性在很大程度上仍不清楚。全基因组整合方法,如基因表达微阵列、基于染色质免疫沉淀的微阵列(ChIP-chip)和染色质免疫沉淀后大规模平行测序(ChIP-seq),为阐明 ES 和 iPS 细胞的多能性、重编程和 DNA 损伤反应机制提供了前所未有的机会。本文总结了关于 ES 和 iPS 细胞的基本生物学问题,并综述了使用全基因组技术的 ES 和 iPS 细胞研究的最新进展。为此,我们对干细胞全基因组研究的未来提出了我们的看法。