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用于干细胞衍生移植物的高灵敏度生物安全模型。

Highly sensitive biosafety model for stem-cell-derived grafts.

作者信息

Lawrenz B, Schiller H, Willbold E, Ruediger M, Muhs A, Esser S

机构信息

CARDION AG, Erkrath, Germany.

出版信息

Cytotherapy. 2004;6(3):212-22. doi: 10.1080/14653240410006031.

Abstract

BACKGROUND

The recent success in the derivation of differentiated cell types from stem cells has raised prospects for the application of regenerative cell therapy. In particular, embryonic stem cells are attractive sources for cell transplantation, due to their immortality and rapid growth. These cells, however, also possess tumorigenic properties, which raises serious safety concerns and makes biosafety testing mandatory. Our goal was to establish a highly sensitive animal model for testing the proliferative potential of stem-cell grafts.

METHODS

BALB/c nude mice received cell grafts of non-neoplastic MRC-5 cells containing defined numbers of mouse embryonic stem cells. We either injected 1 million viable cells into the kidney capsule, or mixed 2 million cells with Matrigel for s.c. transplantation. To analyze the possible impact of an intact immune response on tumor development, we also transplanted the cells into immunocompetent mice. Animals were sacrificed when the tumors became >1 cm and were analyzed in detail.

RESULTS

The nude mouse model reproducibly allowed detection of 20 tumorigenic cells, and even as few as 2 ES cells were found to form teratoma. Interestingly, the administration of cell grafts at two different application sites resulted in different growth kinetics and tumor phenotypes. The highest level of sensitivity (100% detection of 20 tumorigenic ES cells) was achieved by s.c. injection of cells mixed with Matrigel. The influence of the immune system on tumor-cell development was demonstrated by a higher tumor rate of transplants in immunodeficient nude mice compared with immunocompetent mice.

DISCUSSION

We have established a reliable animal model for routine assessment of the biosafety profile of stem-cell-derived cell transplants. This model will facilitate the generation of homogenous non-tumorigenic cell populations, and will help to integrate standardized safety systems into the application of stem-cell-derived grafts for clinical purposes.

摘要

背景

近期从干细胞中成功诱导分化出不同细胞类型,这为再生细胞疗法的应用带来了希望。特别是胚胎干细胞,因其永生性和快速增殖能力,成为细胞移植的理想来源。然而,这些细胞也具有致瘤特性,这引发了严重的安全担忧,使得生物安全性检测成为必需。我们的目标是建立一个高度敏感的动物模型,用于测试干细胞移植的增殖潜力。

方法

将含有特定数量小鼠胚胎干细胞的非肿瘤性MRC - 5细胞移植到BALB/c裸鼠体内。我们要么将100万个活细胞注射到肾包膜内,要么将200万个细胞与基质胶混合进行皮下移植。为了分析完整免疫反应对肿瘤发生的可能影响,我们还将细胞移植到具有免疫能力的小鼠体内。当肿瘤直径超过1厘米时处死动物,并进行详细分析。

结果

裸鼠模型能够可靠地检测到20个致瘤细胞,甚至发现仅2个胚胎干细胞就能形成畸胎瘤。有趣的是,在两个不同的移植部位进行细胞移植,其生长动力学和肿瘤表型有所不同。通过皮下注射与基质胶混合的细胞,实现了最高的灵敏度(100%检测到20个致瘤胚胎干细胞)。与具有免疫能力的小鼠相比,免疫缺陷裸鼠移植后的肿瘤发生率更高,这证明了免疫系统对肿瘤细胞发育的影响。

讨论

我们建立了一个可靠的动物模型,用于常规评估干细胞衍生细胞移植的生物安全性。该模型将有助于生成均匀的非致瘤细胞群体,并有助于将标准化安全系统纳入干细胞衍生移植物的临床应用中。

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