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STAT3 结合的长非编码 RNA lnc-DC 控制人类树突状细胞分化。

The STAT3-binding long noncoding RNA lnc-DC controls human dendritic cell differentiation.

机构信息

National Key Laboratory of Medical Immunology and Institute of Immunology, Second Military Medical University, Shanghai 200433, China.

出版信息

Science. 2014 Apr 18;344(6181):310-3. doi: 10.1126/science.1251456.

Abstract

Long noncoding RNAs (lncRNAs) play important roles in diverse biological processes; however, few have been identified that regulate immune cell differentiation and function. Here, we identified lnc-DC, which was exclusively expressed in human conventional dendritic cells (DCs). Knockdown of lnc-DC impaired DC differentiation from human monocytes in vitro and from mouse bone marrow cells in vivo and reduced capacity of DCs to stimulate T cell activation. lnc-DC mediated these effects by activating the transcription factor STAT3 (signal transducer and activator of transcription 3). lnc-DC bound directly to STAT3 in the cytoplasm, which promoted STAT3 phosphorylation on tyrosine-705 by preventing STAT3 binding to and dephosphorylation by SHP1. Our work identifies a lncRNA that regulates DC differentiation and also broadens the known mechanisms of lncRNA action.

摘要

长链非编码 RNA(lncRNA)在多种生物过程中发挥重要作用;然而,鉴定出能够调节免疫细胞分化和功能的 lncRNA 却很少。在这里,我们鉴定出了 lnc-DC,它仅在人类常规树突状细胞(DC)中表达。lnc-DC 的敲低会损害体外人类单核细胞和体内小鼠骨髓细胞向 DC 的分化,并降低 DC 刺激 T 细胞活化的能力。lnc-DC 通过激活转录因子 STAT3(信号转导和转录激活因子 3)来介导这些效应。lnc-DC 在细胞质中直接与 STAT3 结合,通过阻止 STAT3 与 SHP1 结合和去磷酸化来促进 STAT3 酪氨酸-705 的磷酸化。我们的工作鉴定出一种调节 DC 分化的 lncRNA,也拓宽了 lncRNA 作用的已知机制。

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