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    题名 作者 年代 出处 被引量
1Serine metabolism orchestrates macrophage polarization by regulating the IGF1–p38 axis显示文摘Serine metabolism is reportedly involved in immune cell functions, but whether and how serine metabolism regulates macrophage polarization remain largely unknown. Here, we show that suppressing serine metabolism, either by inhibiting the activity of the key enzyme phosphoglycerate dehydrogenase in the serine biosynthesis pathway or by exogenous serine and glycine restriction, robustly enhances the polarization of interferon-γ-activated macrophages (M(IFN-γ)) but suppresses that of interleukin-4-activated macrophages (M(IL-4)) both in vitro and in vivo. Mechanistically, serine metabolism deficiency increases the expression of IGF1 by reducing the promoter abundance of S-adenosyl methionine-dependent histone H3 lysine 27 trimethylation. IGF1 then activates the p38-dependent JAK–STAT1 axis to promote M(IFN-γ) polarization and suppress STAT6-mediated M(IL-4) activation. This study reveals a new mechanism by which serine metabolism orchestrates macrophage polarization and suggests the manipulation of serine metabolism as a therapeutic strategy for macrophage-mediated immune diseases.Xiao Shan Penghui Hu Lina Ni Long Shen Yanan Zhang Zemin Ji Yan Cui Meihua Guo Haoan Wang Liyuan Ran Kun Yang Ting Wang Lei Wang Bin Chen Zhi Yao Vingjie Wu Qiujing Yu 2022Cellular & Molecular Immunology2022,19,11:5
2The DFF-PSP Iterative Separation and Theoretical Bound for PCMA with Long Memory显示文摘This paper proposes the Decision feedbackfeedforward per-survivor processing(DFF-PSP) iterative separation algorithm and the Monte Carlo integrationbased method to compute the theoretical bound for Paired carrier multiple access(PCMA) Single channel blind separation(SCBS) which is highly complex with long memory. The truncated PSP is employed while the pre- and post- cursors are disregarded to control the complexity.The delayed decisions feedforward and local decisions feedback filters are designed to process the pre- and postcursors. The Bit-interleaved code modulation iterative decoder(BICM-ID) is combined with the second soft decision of the truncated PSP to obtain a better performance.The mixture signal model is regarded as a Multiple-access channel(MAC) with memory, and the theoretical performance bound is obtained via entropy inequality, Monte Carlo integration and Fano inequality. Simulation results show that the DFF-PSP iterative separation provides the good tradeoff between complexity and performance.CUI Penghui JIANG Hua CAO Kai LI Taozhu 2016Chinese Journal of Electronics2016,25,5:3
3Dressing Technology on the Diamond Abrasive Grinding Wheels Using the Rotary Diamond Dresser 显示文摘Zhongming Cui Penghui Deng Lei Du 2009Key Engineering Materials2009,,416:1
4Bibliometric analysis on scientific productivity of NIMTE,CAS显示文摘LV Penghui QIU Huabing CUI Ping 2010Geomatics and In- formation Science of Wuhan University2010,35,11:1
5Whole‑genome transcriptome and DNA methylation dynamics of pre‑implantation embryos reveal progression of embryonic genome activation in buffaloes显示文摘Background During mammalian pre-implantation embryonic development(PED),the process of maternal-to-zygote transition(MZT)is well orchestrated by epigenetic modification and gene sequential expression,and it is related to the embryonic genome activation(EGA).During MZT,the embryos are sensitive to the environment and easy to arrest at this stage in vitro.However,the timing and regulation mechanism of EGA in buffaloes remain obscure.Results Buffalo pre-implantation embryos were subjected to trace cell based RNA-seq and whole-genome bisulfite sequencing(WGBS)to draw landscapes of transcription and DNA-methylation.Four typical developmental steps were classified during buffalo PED.Buffalo major EGA was identified at the 16-cell stage by the comprehensive analy-sis of gene expression and DNA methylation dynamics.By weighted gene co-expression network analysis,stage-spe-cific modules were identified during buffalo maternal-to-zygotic transition,and key signaling pathways and biological process events were further revealed.Programmed and continuous activation of these pathways was necessary for success of buffalo EGA.In addition,the hub gene,CDK1,was identified to play a critical role in buffalo EGA.Conclusions Our study provides a landscape of transcription and DNA methylation in buffalo PED and reveals deeply the molecular mechanism of the buffalo EGA and genetic programming during buffalo MZT.It will lay a foundation for improving the in vitro development of buffalo embryos.Penghui Fu Du Zhang Chunyan Yang Xiang Yuan Xier Luo Haiying Zheng Yanfei Deng Qingyou Liu Kuiqing Cui Fei Gao Deshun Shi 2023Journal of Animal Science and Biotechnology2023,14,6:0
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