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Stem Cells International
Volume 2016 (2016), Article ID 9586751, 13 pages
http://dx.doi.org/10.1155/2016/9586751
Research Article

Differentiation-Associated MicroRNA Alterations in Mouse Heart-Derived Sca-1+CD31 and Sca-1+CD31+ Cells

Qiong Wu,1,2,3 Jinxi Zhan,1,2,3 Yun Li,1,2,3 Xiaoxia Wang,1,2,3 Lu Xu,4 Juan Yu,1,2,3 Shiming Pu,1,2,3 and Zuping Zhou1,2,3

1School of Life Sciences, Guangxi Normal University, Guilin 541004, China
2Guangxi Universities Key Laboratory of Stem Cell and Biopharmaceutical Technology, Guangxi Normal University, Guilin 541004, China
3Research Center for Biomedical Sciences, Guangxi Normal University, Guilin 541004, China
4Jilin Medical College, Jilin 132013, China

Received 22 November 2015; Revised 2 March 2016; Accepted 20 March 2016

Academic Editor: Tobias Cantz

Copyright © 2016 Qiong Wu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplementary Material

Figure S1. Differentiation potential of Sca-1+CD31+cells by FACS into cardiomyocyte, smooth muscle, and endothelial cells in vitro.

Table S1. The differently expressed miRNAs between Sca1+CD31−and Sca1+CD31+ cells.

Table S2. KEGG pathway analyses of predicted miRNA targets.

Table S3. Pathway of the differently expressed miRNAs (the top 20 pathway) and their corresponding target genes.

Table S4. Cluster of the differently expressed miRNAs (the top 20 GO terms) and their corresponding target genes.

Table S5. The differently expressed mRNAs between Sca1+CD31−and Sca1+CD31+ cells.

Table S6. Pathway of the differently expressed mRNAs (the top 20 pathway) and their corresponding genes.

Table S7. Cluster of the differently expressed mRNAs (the top 20 GO terms) and their corresponding genes.

  1. Supplementary Material