miR-15b and miR-16 are implicated in activation of the rat hepatic stellate cell: An essential role for apoptosis

被引:257
作者
Guo, Can-Jie
Pan, Qin [1 ]
Li, Ding-Guo
Sun, Hua
Liu, Bo-Wei
机构
[1] Shanghai Jiao Tong Univ, Digest Dis Lab, Xinhua Hosp, Sch Med, Shanghai 200092, Peoples R China
关键词
Hepatic stellate cells; Activation; miR-16; miR-15b; Gene ontology; Bcl-2; Caspase; Apoptosis; GENE-EXPRESSION; GROWTH-FACTOR; MICRORNAS; QUANTIFICATION; FIBROGENESIS; RESISTANCE; FIBROSIS;
D O I
10.1016/j.jhep.2008.11.025
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: To reveal the microRNA (miRNA) expression profile and related roles in rat HSCs during activation. Methods: miRNA expression profiling was analyzed in quiescent and in culture-activated HSCs by microarray. The differentially expressed miRNAs, as verified by RT-PCR, were subjected to gene ontology (GO) analysis. Furthermore, the effects of miR-16 and miR-15b on the apoptosis of activated HSCs were investigated by Hoechst 33258, TUNEL staining and annexin-V/PI labeling flow cytometry. The underlying mechanism related to Bcl-2 and caspases was assessed. Results: The upregulated and downregulated miRNAs in activated HSCs were 12 miRNAs and 9 miRNAs, respectively. The differential expression of miR-16, -15b, -122, -138, -143, and -140 was validated. High-enrichment GOs containing apoptosis-related targeted genes and miRNA-gene networks characterized by Bcl-2, which was targeted by the miR-15/16 family, uncovered the critical role of miR-16 and miR-15b in apoptosis. Restoring the intracellular miRNAs by miR-16 and miR-15b administration greatly reduced Bcl-2, and increased the expression of caspases 3, 8, and 9. Significantly elevated rates of apoptosis were then induced in activated HSCs. Conclusions:The activation of HSCs relate to 21 miRNAs. Among these, mir-15b and miR-16 may be essential for apoptosis by targeting Bcl-2 and the caspase signaling pathway. (c) 2009 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:766 / 778
页数:13
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