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DNA damage by X-rays and their impact on replication processes.X 射线对 DNA 的损伤及其对复制过程的影响。
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DNA-SCARS: distinct nuclear structures that sustain damage-induced senescence growth arrest and inflammatory cytokine secretion.DNA-SCARS:维持损伤诱导衰老生长停滞和炎性细胞因子分泌的独特核结构。
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人类胚胎干细胞及其分化后代对电离辐射的反应。

Responses of human embryonic stem cells and their differentiated progeny to ionizing radiation.

机构信息

Buck Institute for Research on Aging, Novato, CA 94945, USA.

出版信息

Biochem Biophys Res Commun. 2012 Sep 14;426(1):100-5. doi: 10.1016/j.bbrc.2012.08.043. Epub 2012 Aug 14.

DOI:10.1016/j.bbrc.2012.08.043
PMID:22917535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3498829/
Abstract

Human embryonic stem cells (hESCs) hold promise for the treatment of many human pathologies. For example, hESCs and the neuronal stem cells (NSCs) and neurons derived from them have significant potential as transplantation therapies for a variety of neurodegenerative diseases. Two concerns about the use of hESCs and their differentiated derivatives are their ability to function and their ability to resist neoplastic transformation in response to stresses that inevitably arise during their preparation for transplantation. To begin to understand how these cells handle genotoxic stress, we examined the responses of hESCs and derived NSCs and neurons to ionizing radiation (IR). Undifferentiated hESCs were extremely sensitive to IR, with nearly all the cells undergoing cell death within 5-7 h. NSCs and neurons were substantially more resistant to IR, with neurons showing the most resistant. Of interest, NSCs that survived IR underwent cellular senescence and acquired astrocytic characteristics. Unlike IR-treated astrocytes, however, the NSC-derived astrocytic cells that survived IR did not display the typical pro-inflammatory, pro-carcinogenic senescence-associated secretory phenotype. These findings suggest distinct genotoxic stress-responses of hESCs and derived NSC and neuronal populations, and suggest that damaged NSCs, while failing to function, may not cause local inflammation.

摘要

人类胚胎干细胞(hESCs)在治疗许多人类病理方面具有广阔的应用前景。例如,hESCs 及其衍生的神经干细胞(NSCs)和神经元在各种神经退行性疾病的移植治疗中具有巨大的潜力。使用 hESCs 及其分化衍生物存在两个顾虑,一是它们的功能能力,二是在准备移植过程中,它们抵抗肿瘤转化的能力。为了开始了解这些细胞如何应对遗传毒性应激,我们研究了 hESCs 及其衍生的 NSCs 和神经元对电离辐射(IR)的反应。未分化的 hESCs 对 IR 极其敏感,几乎所有细胞在 5-7 小时内都会死亡。NSCs 和神经元对 IR 的抵抗力要强得多,其中神经元的抵抗力最强。有趣的是,存活下来的 NSCs 经历了细胞衰老并获得了星形胶质细胞的特征。然而,与 IR 处理的星形胶质细胞不同,存活下来的 IR 处理的 NSC 衍生的星形胶质细胞并没有表现出典型的促炎、促癌的衰老相关分泌表型。这些发现表明 hESCs 及其衍生的 NSCs 和神经元群体具有不同的遗传毒性应激反应,并表明受损的 NSCs 虽然无法发挥功能,但可能不会引起局部炎症。