PI3K/AKT/mTOR通路
生物
先天免疫系统
糖酵解
蛋白激酶B
厌氧糖酵解
免疫
碳水化合物代谢
细胞生物学
单核细胞
新陈代谢
葡萄糖摄取
免疫系统
生物化学
免疫学
信号转导
胰岛素
内分泌学
作者
Shih‐Chin Cheng,Jessica Quintin,Robert A. Cramer,Kelly M. Shepardson,Sadia Saeed,Vinod Kumar,Evangelos J. Giamarellos‐Bourboulis,Joost H.A. Martens,Nagesha Rao,Ali Aghajanirefah,Ganesh R. Manjeri,Li Yang,Daniela C. Ifrim,Rob J.W. Arts,Brian M. J. W. van der Veer,Peter M.T. Deen,Colin Logie,Luke O'neill,Peter H.G.M. Willems,Frank L. van de Veerdonk
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2014-09-25
卷期号:345 (6204): 1250684-1250684
被引量:2041
标识
DOI:10.1126/science.1250684
摘要
A BLUEPRINT of immune cell development To determine the epigenetic mechanisms that direct blood cells to develop into the many components of our immune system, the BLUEPRINT consortium examined the regulation of DNA and RNA transcription to dissect the molecular traits that govern blood cell differentiation. By inducing immune responses, Saeed et al. document the epigenetic changes in the genome that underlie immune cell differentiation. Cheng et al. demonstrate that trained monocytes are highly dependent on the breakdown of sugars in the presence of oxygen, which allows cells to produce the energy needed to mount an immune response. Chen et al. examine RNA transcripts and find that specific cell lineages use RNA transcripts of different length and composition (isoforms) to form proteins. Together, the studies reveal how epigenetic effects can drive the development of blood cells involved in the immune system. Science , this issue 10.1126/science.1251086 , 10.1126/science.1250684 , 10.1126/science.1251033
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