Comparison of long noncoding RNA and mRNA expression profiles in mesenchymal stem cells derived from human periodontal ligament and bone marrow.
Comparison of long noncoding RNA and mRNA expression profiles in mesenchymal stem cells derived from human periodontal ligament and bone marrow.
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人牙周膜和骨髓来源的间充质干细胞中长非编码 RNA 和 mRNA 表达谱的比较
DOI:
10.1155/2014/317853
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发表时间:
2014
影响因子:
--
通讯作者:
Fan Z
中科院分区:
文献类型:
--
作者:
Dong R;Du J;Wang L;Wang J;Ding G;Wang S;Fan Z
Mesenchymal stem cells (MSCs) in different anatomic locations possess diverse biological activities. Maintaining the pluripotent state and differentiation depend on the expression and regulation of thousands of genes, but it remains unclear which molecular mechanisms underlie MSC diversity. Thus, potential MSC applications are restricted. Long noncoding RNAs (lncRNAs) are implicated in the complex molecular circuitry of cellular processes. We investigated differences in lncRNA and mRNA expression profiles between bone marrow stem cells (BMSCs) and periodontal ligament stem cells (PDLSCs) with lncRNA microarray assays and bioinformatics analysis. In PDLSCs, numerous lncRNAs were significantly upregulated (n = 457) or downregulated (n = 513) compared to BMSCs. Furthermore, 1,578 mRNAs were differentially expressed. These genes implicated cellular pathways that may be associated with MSC characteristics, including apoptosis, MAPK, cell cycle, and Wnt signaling pathway. Signal-net analysis indicated that phospholipase C beta 4, filamin B beta, calcium/calmodulin-dependent protein kinase II gamma, and the ionotropic glutamate receptor, AMPA 1, had the highest betweenness centrality among significant genes in the differential gene profile network. A comparison between the coding-noncoding gene coexpression networks of PDLSCs and BMSCs identified chemokine (C-X-C motif) ligand 12 as a core regulatory factor in MSC biology. These results provided insight into the mechanisms underlying MSC biology.
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影响因子:
4.3
作者:
Kim, Su-Hwan;Kim, Kyoung-Hwa;Lee, Yong-Moo
通讯作者:
Lee, Yong-Moo
影响因子:
4.2
作者:
Hayashi, Ousuke;Katsube, Yoshihiro;Ito, Hiromoto
通讯作者:
Ito, Hiromoto
影响因子:
12.4
作者:
d'Aquino, R.;Graziano, A.;Papaccio, G.
通讯作者:
Papaccio, G.
影响因子:
4.3
作者:
Kawaguchi, H;Hirachi, A;Kurihara, H
通讯作者:
Kurihara, H
影响因子:
--
作者:
Caplan, AI
通讯作者:
Caplan, AI