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小鼠树突状细胞发育的微小RNA表达图谱。

A microRNA expression atlas of mouse dendritic cell development.

作者信息

Johanson Timothy M, Cmero Marek, Wettenhall James, Lew Andrew M, Zhan Yifan, Chong Mark M W

机构信息

1] Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia [2] Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia [3] Immunology and Diabetes, St Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.

Immunology and Diabetes, St Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.

出版信息

Immunol Cell Biol. 2015 May-Jun;93(5):480-5. doi: 10.1038/icb.2014.109. Epub 2014 Dec 23.

Abstract

Dendritic cells (DCs) are sentinel cells of the immune system and are essential for inducing a proper immune response. The mechanisms driving the development of DCs are not fully understood. Although the roles of cytokines and transcription factors have been a major focus, there is now substantial interest in the role of microRNAs (miRNAs). miRNAs are small RNAs that regulate gene expression by targeting messenger RNAs for translational repression and ultimately degradation. By means of deep sequencing, we have assembled a comprehensive and quantitative resource of miRNA expression during DC development. We show that mature DCs and their hematopoietic progenitors can be distinguished based on miRNA expression profiles. On the other hand, we show that functionally distinct conventional and plasmacytoid DC subsets are indistinguishable based on miRNA profile. In addition, we identify differences between ex vivo purified conventional DCs and their in vitro Flt3L-generated counterparts. This miRNA expression atlas will provide a valuable resource for the study of miRNAs in DC development and function.

摘要

树突状细胞(DCs)是免疫系统的哨兵细胞,对于诱导适当的免疫反应至关重要。驱动DCs发育的机制尚未完全了解。尽管细胞因子和转录因子的作用一直是主要研究重点,但现在人们对微小RNA(miRNAs)的作用也产生了浓厚兴趣。miRNAs是一类小RNA,通过靶向信使RNA进行翻译抑制并最终降解来调节基因表达。通过深度测序,我们构建了DCs发育过程中miRNA表达的全面定量资源。我们表明,成熟DCs及其造血祖细胞可以根据miRNA表达谱进行区分。另一方面,我们表明,基于miRNA谱,功能不同的传统DC亚群和浆细胞样DC亚群无法区分。此外,我们确定了体外纯化的传统DCs与其体外Flt3L诱导生成的对应细胞之间的差异。这个miRNA表达图谱将为研究miRNAs在DCs发育和功能中的作用提供宝贵资源。

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