4.5 Article

MicroRNA let-7i regulates dendritic cells maturation targeting interleukin-10 via the Janus kinase 1-signal transducer and activator of transcription 3 signal pathway subsequently induces prolonged cardiac allograft survival in rats

期刊

JOURNAL OF HEART AND LUNG TRANSPLANTATION
卷 35, 期 3, 页码 378-388

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.healun.2015.10.041

关键词

MicroRNA let-7i; IL-10; JAK1-STAT3; dendritic cell; heart transplantation; tolerance; rat

资金

  1. National Natural Science Foundation-Youth Foundation of China [81200240]
  2. New Century Excellent Talents in University Foundation, Heilongliang Province [1254NCET014]
  3. National Science Foundation for Post-doctoral Scientists of China [2013T60391]
  4. Key Laboratory of Myocardial Ischemia
  5. Chinese Ministry of Education, Harbin, Heilongjiang Province, China [KF201208, KF201405, KF201406]
  6. Natural Science Foundation of Heilongjiang Province of China [H2015048]

向作者/读者索取更多资源

BACKGROUND: In this study, we investiglated whether microRNA let-7i regulates dendric cell maturation targeting interleukin-10 (IL-10) via the Janus kinase 1 signal transducer and activator of transcription 3 (JAK1-STAT3) signal pathway subsequently prolongs rat cardiac allograft survival. METHODS: Quantitative real-time reverse transcriptase polymerase chain reaction, enzyme linked immunosorbent assay, and dual-luciferase assay were performed to verify whether IL-10 was the target of let-7i, and regulatory T cells were assessed by flow cytometry and immunohistochemical study. Western blot was performed to detect JAK1, STAT3, and phosphorylated STAT3 expression. Lewis recipients of Dark Agouti hearts were transfused with phosphate-buffered saline, lipopolysaccharide (LPS)-mature dendritic cells (mDCs), or let-7i-inhibitor-mDCs. Allograft survival times were recorded, and histologic studies were performed. RESULTS: Expression of IL-10 messenger RNA level and production of IL-10 were increased in let-7i inhibitor-mDCs compared with LPS-mDCs. Luciferase activity showed that the translational level of the IL-10 luciferase reporter was decreased by let-7i mimic but increased by let-7i-inhibitor. MicroRNA let 7i inhibitor suppressed DC maturation; however, pretreatment of IL-10 small interfering RNA attenuated the suppression. Expression of JAK1, STAT3, and phosphorylated STAT3 in mDCs were suppressed by let-7i mimic, and pre-treatment of IL-10 small interfering RNA, however, were upregulated by let-7i inhibitor. Lewis recipients transfused with let-7i inhibitor-mDCs significantly prolonged Dark Agouti cardiac allograft survival. The allografts transfused with let-7i inhibitor-mDCs showed slight cell infiltration and significantly preserved graft structure. Inhibition of let-7i increased CD4(+)CD25(+)forIchead box P3(+) regulatory T cells and modulated cytokine profiles in vivo and in vitro. CONCLUSIONS: MicroRNA let-7i regulated DC maturation and function targeting IL-10 through the JAK1-STAT3 pathway. Moreover, transfusion of LPS-induced mDCs transfected with let-7i inhibitor induced prolonged cardiac allograft s'urvival and generated regulatory T cells. (C) 2016 International Society for Heart and Lung Transplantation. All rights reserved.

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