Suppr超能文献

利用piggyBac系统在能够进行T细胞谱系分化的恒河猴诱导多能干细胞中实现有效且稳定的基因转导。

Effective and stable gene transduction in rhesus macaque iPSCs capable of T-lineage differentiation utilizing the piggyBac system.

作者信息

Tanaka Masahiro, Iwamoto Yoshihiro, Wang Bo, Imai Eri, Yoshida Munehiro, Iriguchi Shoichi, Kaneko Shin

机构信息

Shin Kaneko Laboratory, Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.

Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

出版信息

Regen Ther. 2024 Mar 18;27:104-111. doi: 10.1016/j.reth.2024.03.002. eCollection 2024 Dec.

Abstract

INTRODUCTION

Genetically modified human induced pluripotent stem cell (iPSC)-based regenerative medicine has substantial potential in the treatment of refractory human diseases. Thus, preclinical studies on the safety and efficacy of these products are essential. Non-human primate (NHP) models such as the rhesus macaque are highly similar to humans in terms of size, lifespan, and immune system, rendering them superior models. However, effective gene transduction in rhesus macaque iPSCs (Rh-iPSCs) remains challenging. In this study, we investigated the effective gene transduction into Rh-iPSCs and its effect on differentiation efficiency.

METHODS

We established a gene transduction method using the piggyBac transposon vector system. Gene transduced Rh-iPSCs were analyzed for undifferentiated markers. We did teratoma assay to check pluripotency. Gene transduced Rh-iPSCs were differentiated into hematopoietic stem and progenitor cells (HSPCs) and T-cell lineage cells. Additionally, gene transduced Rh-iPSCs were compared the differentiation efficiency with parental Rh-iPSCs.

RESULTS

We could establish a gene transduction method using the piggyBac transposon vector system, demonstrating high efficiency and stable transgene expression in Rh-iPSCs. These Rh-iPSCs maintained long-term gene expression while expressing undifferentiated markers. Teratoma assay indicated that these Rh-iPSCs had pluripotency. These Rh-iPSCs could differentiate into HPSCs and T cells that express transgenes. These Rh-iPSCs can differentiate into hematopoietic stem cells and T cells that express transgenes. No significant differences in efficiency of differentiation were observed between parental Rh-iPSCs and these Rh-iPSCs.

CONCLUSIONS

These results indicate that the piggyBac transposon vector is an excellent gene transfer tool for rhesus macaque iPSCs and could contribute to the advancement of preclinical studies using rhesus macaque iPSCs.

摘要

引言

基于基因编辑的人类诱导多能干细胞(iPSC)的再生医学在治疗难治性人类疾病方面具有巨大潜力。因此,对这些产品的安全性和有效性进行临床前研究至关重要。恒河猴等非人灵长类动物(NHP)模型在大小、寿命和免疫系统方面与人类高度相似,使其成为更优的模型。然而,在恒河猴iPSC(Rh-iPSC)中进行有效的基因转导仍然具有挑战性。在本研究中,我们研究了向Rh-iPSC中进行有效基因转导及其对分化效率的影响。

方法

我们建立了一种使用piggyBac转座子载体系统的基因转导方法。对基因转导的Rh-iPSC进行未分化标志物分析。我们进行了畸胎瘤试验以检查多能性。将基因转导的Rh-iPSC分化为造血干细胞和祖细胞(HSPC)以及T细胞谱系细胞。此外,将基因转导的Rh-iPSC与亲代Rh-iPSC的分化效率进行比较。

结果

我们可以使用piggyBac转座子载体系统建立一种基因转导方法,证明在Rh-iPSC中具有高效且稳定的转基因表达。这些Rh-iPSC在表达未分化标志物的同时保持长期基因表达。畸胎瘤试验表明这些Rh-iPSC具有多能性。这些Rh-iPSC可以分化为表达转基因的HPSC和T细胞。这些Rh-iPSC可以分化为表达转基因的造血干细胞和T细胞。在亲代Rh-iPSC和这些Rh-iPSC之间未观察到分化效率的显著差异。

结论

这些结果表明,piggyBac转座子载体是用于恒河猴iPSC的优秀基因转移工具,并且可以促进使用恒河猴iPSC的临床前研究的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/10966093/309e1ed26d0a/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验