Derivation of induced pluripotent stem cells from human peripheral blood T lymphocytes.

Derivation of induced pluripotent stem cells from human peripheral blood T lymphocytes.
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DOI:
10.1371/journal.pone.0011373
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发表时间:
2010-06-29
期刊:
影响因子:
3.7
通讯作者:
Nuwaysir EF
Nuwaysir EF
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Brown ME;Rondon E;Rajesh D;Mack A;Lewis R;Feng X;Zitur LJ;Learish RD;Nuwaysir EF

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Induced pluripotent stem cells (iPSCs) hold enormous potential for the development of personalized in vitro disease models, genomic health analyses, and autologous cell therapy. Here we describe the generation of T lymphocyte-derived iPSCs from small, clinically advantageous volumes of non-mobilized peripheral blood. These T-cell derived iPSCs (“TiPS”) retain a normal karyotype and genetic identity to the donor. They share common characteristics with human embryonic stem cells (hESCs) with respect to morphology, pluripotency-associated marker expression and capacity to generate neurons, cardiomyocytes, and hematopoietic progenitor cells. Additionally, they retain their characteristic T-cell receptor (TCR) gene rearrangements, a property which could be exploited for iPSC clone tracking and T-cell development studies. Reprogramming T-cells procured in a minimally invasive manner can be used to characterize and expand donor specific iPSCs, and control their differentiation into specific lineages.
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