A Medium-Throughput Analysis of Signaling Pathways Involved in Early Stages of Stem Cell Reprogramming

被引:5
|
作者
Fritz, Ashley L. [1 ]
Mao, Sunnie R. [1 ]
West, Mary G. [2 ]
Schaffer, David V. [1 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Berkeley Stem Cell Ctr, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
induced pluripotent stem cells; reprogramming; signal transduction; SELF-RENEWAL; TUMOR-SUPPRESSOR; PROGENITOR PROLIFERATION; SOMATIC-CELLS; IN-VITRO; STAT3; DIFFERENTIATION; PLURIPOTENCY; PROTEIN; ACTIVATION;
D O I
10.1002/bit.25336
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
The induction of pluripotency from adult cells has enormous potential in regenerative medicine. While initial efforts to study mechanisms and improve efficiency of induced pluripotent stem cell (iPSC) reprogramming focused on the direct roles of transcriptional regulators, increasing evidence indicates that cellular signal transduction pathways can modulate this process. Here, we present a medium-throughput system to study the effect of signaling pathways on the early stages of reprogramming. We generated a set of lentiviral vectors encoding 38 genes that upregulate or downregulate major signal transduction pathways and quantified each signaling factor's effect on reprogramming. This approach confirmed the role of several factors previously implicated in reprogramming, as well as identified several GTPases-factors that to date have not been largely studied in reprogramming-that improve or hinder iPSC reprogramming. In addition, this methodology is useful in determining new targets for enhancing pluripotency reprogramming, lineage reprogramming, and/or cell differentiation. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:209 / 219
页数:11
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