Gene Expression Profile and Functionality of ESC-Derived Lin-ckit+Sca-1+Cells Are Distinct from Lin-ckit+Sca-1+Cells Isolated from Fetal Liver or Bone Marrow

被引:1
|
作者
Fernandez, Irina [1 ]
Fridley, Krista M. [1 ]
Arasappan, Dhivya [4 ]
Ambler, Rosalind V. [1 ]
Tucker, Philip W. [2 ,3 ]
Roy, Krishnendu [1 ,3 ]
机构
[1] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mol Genet & Microbiol, Austin, TX 78712 USA
[3] Univ Texas Austin, Inst Cell & Mol Biol, Austin, TX 78712 USA
[4] Univ Texas Austin, Genome Sequencing & Anal Facil, Austin, TX 78712 USA
来源
PLOS ONE | 2012年 / 7卷 / 12期
基金
美国国家卫生研究院;
关键词
HEMATOPOIETIC STEM-CELLS; DEFINITIVE HEMATOPOIESIS; DIFFERENTIATION; PROGENITORS; CULTURE; IDENTIFICATION; PURIFICATION; EXPANSION; SCAFFOLD; ORIGINS;
D O I
10.1371/journal.pone.0051944
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In vitro bioreactor-based cultures are being extensively investigated for large-scale production of differentiated cells from embryonic stem cells (ESCs). However, it is unclear whether in vitro ESC-derived progenitors have similar gene expression profiles and functionalities as their in vivo counterparts. This is crucial in establishing the validity of ESC-derived cells as replacements for adult-isolated cells for clinical therapies. In this study, we compared the gene expression profiles of Lin-ckit+Sca-1+ (LKS) cells generated in vitro from mouse ESCs using either static or bioreactor-based cultures, with that of native LKS cells isolated from mouse fetal liver (FL) or bone marrow (BM). We found that in vitro-generated LKS cells were more similar to FL-than to BM LKS cells in gene expression. Further, when compared to cells derived from bioreactor cultures, static culture-derived LKS cells showed fewer differentially expressed genes relative to both in vivo LKS populations. Overall, the expression of hematopoietic genes was lower in ESC-derived LKS cells compared to cells from BM and FL, while the levels of non-hematopoietic genes were up-regulated. In order to determine if these molecular profiles correlated with functionality, we evaluated ESC-derived LKS cells for in vitro hematopoietic-differentiation and colony formation (CFU assay). Although static culture-generated cells failed to form any colonies, they did differentiate into CD11c+ and B220+ cells indicating some hematopoietic potential. In contrast, bioreactor-derived LKS cells, when differentiated under the same conditions failed to produce any B220+ or CD11c+ cells and did not form colonies, indicating that these cells are not hematopoietic progenitors. We conclude that in vitro culture conditions significantly affect the transcriptome and functionality of ESC-derived LKS cells and although in vitro differentiated LKS cells were lineage negative and expressed both ckit and Sca-1, these cells, especially those obtained from dynamic cultures, are significantly different from native cells of the same phenotype.
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页数:11
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