Cell type of origin influences the molecular and functional properties of mouse induced pluripotent stem cells

被引:889
作者
Polo, Jose M. [1 ,2 ,3 ,4 ,5 ,6 ]
Liu, Susanna [7 ]
Figueroa, Maria Eugenia [8 ]
Kulalert, Warakorn [1 ,2 ,3 ,4 ,5 ,6 ]
Eminli, Sarah [1 ,2 ,3 ,4 ,5 ,6 ]
Tan, Kah Yong [1 ,2 ,3 ,6 ,9 ]
Apostolou, Effie [1 ,2 ,3 ,4 ,5 ,6 ]
Stadtfeld, Matthias [1 ,2 ,3 ,4 ,5 ,6 ]
Li, Yushan [8 ]
Shioda, Toshi [4 ]
Natesan, Sridaran [10 ]
Wagers, Amy J. [1 ,2 ,3 ,6 ,9 ]
Melnick, Ari [8 ]
Evans, Todd [7 ]
Hochedlinger, Konrad [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
[4] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA USA
[5] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[6] Harvard Stem Cell Inst, Cambridge, MA USA
[7] Weill Cornell Med Coll, Dept Surg, New York, NY USA
[8] Weill Cornell Med Coll, Dept Med, Div Hematol Oncol, New York, NY USA
[9] Joslin Diabet Ctr, Boston, MA 02215 USA
[10] Sanofi Aventis Cambridge Genom Ctr, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; EPIGENETIC MEMORY; DNA METHYLATION; GENERATION; DIFFERENTIATION; INDUCTION; EFFICIENT; CHROMATIN; ABSENCE; SYSTEM;
D O I
10.1038/nbt.1667
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Induced pluripotent stem cells (iPSCs) have been derived from various somatic cell populations through ectopic expression of defined factors. It remains unclear whether iPSCs generated from different cell types are molecularly and functionally similar. Here we show that iPSCs obtained from mouse fibroblasts, hematopoietic and myogenic cells exhibit distinct transcriptional and epigenetic patterns. Moreover, we demonstrate that cellular origin influences the in vitro differentiation potentials of iPSCs into embryoid bodies and different hematopoietic cell types. Notably, continuous passaging of iPSCs largely attenuates these differences. Our results suggest that early-passage iPSCs retain a transient epigenetic memory of their somatic cells of origin, which manifests as differential gene expression and altered differentiation capacity. These observations may influence ongoing attempts to use iPSCs for disease modeling and could also be exploited in potential therapeutic applications to enhance differentiation into desired cell lineages.
引用
收藏
页码:848 / U130
页数:10
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