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首页> 外文期刊>Stem Cell Reviews and Reports >Unravelling the Pluripotency Paradox in Fetal and Placental Mesenchymal Stem Cells: Oct-4 Expression and the Case of the Emperor’s New Clothes
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Unravelling the Pluripotency Paradox in Fetal and Placental Mesenchymal Stem Cells: Oct-4 Expression and the Case of the Emperor’s New Clothes

机译:揭示胎儿和胎盘间充质干细胞的多能性悖论:Oct-4表达和皇帝的新衣着

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摘要

Mesenchymal stem cells (MSC) from fetal-placental tissues have translational advantages over their adult counterparts, and have variably been reported to express pluripotency markers. OCT- 4 expression in fetal-placental MSC has been documented in some studies, paradoxically without tumourogenicity in vivo. It is possible that OCT- 4 expression is insufficient to induce true “stemness”, but this issue is important for the translational safety of fetal-derived MSC. To clarify this, we undertook a systematic literature review on OCT- 4 in fetal or adnexal MSC to show that most studies report OCT- 4 message or protein expression, but no study provides definitive evidence of true OCT- 4A expression. Discrepant findings were attributable not to different culture conditions, tissue sources, or gestational ages but instead to techniques used. In assessing OCT- 4 as a pluripotency marker, we highlight the challenges in detecting the correct OCT- 4 isoform (OCT- 4A) associated with pluripotency. Although specific detection of OCT- 4A mRNA is achievable, it appears unlikely that any antibody can reliably distinguish between OCT- 4A and the pseudogene OCT- 4B. Finally, using five robust techniques we demonstrate that fetal derived-MSC do not express OCT- 4A (or by default OCT- 4B). Reports suggesting OCT- 4 expression in fetal-derived MSC warrant reassessment, paying attention to gene and protein isoforms, pseudogenes, and antibody choice as well as primer design. Critical examination of the OCT- 4 literature leads us to suggest that OCT- 4 expression in fetal MSC may be a case of “The Emperor’s New Clothes” with early reports of (false) positive expression amplified in subsequent studies without critical attention to emerging refinements in knowledge and methodology.
机译:胎儿-胎盘组织的间充质干细胞(MSC)较其成年的同种细胞具有翻译优势,并且据报道有多种表达多能性标志物的报道。在一些研究中已经证明了胎儿-胎盘MSC中的OCT- 4表达,但自相矛盾的是在体内没有致瘤性。 OCT- 4的表达可能不足以诱导真正的“干性”,但是这个问题对于胎儿来源的MSC的翻译安全性很重要。为了澄清这一点,我们对胎儿或附件MSC中的OCT- 4进行了系统的文献综述,以显示大多数研究报告了OCT- 4信息或蛋白质表达,但没有研究提供确凿的OCT- 4A表达的证据。不一致的发现并非归因于不同的培养条件,组织来源或胎龄,而是归因于所使用的技术。在评估OCT- 4作为多能性标志物时,我们重点介绍了检测与多能性相关的正确OCT- 4同工型(OCT- 4A)的挑战。尽管可以实现OCT- 4A mRNA的特异性检测,但似乎没有任何抗体能够可靠地区分OCT- 4A和假基因OCT- 4B。最后,使用五种可靠的技术,我们证明胎儿衍生的MSC不表达OCT- 4A(或默认情况下为OCT- 4B)。报道提示胎儿来源的MSC中OCT- expression4表达需要重新评估,注意基因和蛋白质同工型,假基因,抗体选择以及引物设计。对OCT- 4文献的严格检查使我们认为,胎儿MSC中的OCT- 4表达可能是“皇帝的新衣”的例子,早期报道(假)阳性表达在随后的研究中得到了放大,而没有对新出现的改进给予严格的关注。在知识和方法论上。

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  • 来源
    《Stem Cell Reviews and Reports》 |2013年第4期|408-421|共14页
  • 作者单位

    UQ Centre for Clinical Research University of Queensland Herston campus">(1);

    UQ Centre for Clinical Research University of Queensland Herston campus">(1);

    Fetal Stem Cell Therapy Group Institute of Reproductive Developmental Biology">(2);

    UQ Centre for Clinical Research University of Queensland Herston campus">(1);

    Experimental Fetal Medicine Group Department of Obstetrics Gynaecology Yong Loo Lin School of Medicine National University of Singapore">(3);

    Department of Reproductive Medicine KK Women’s and Children’s Hospital">(4);

    UQ Centre for Clinical Research University of Queensland Herston campus">(1);

    Experimental Fetal Medicine Group Department of Obstetrics Gynaecology Yong Loo Lin School of Medicine National University of Singapore">(3);

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