炎症
牙周炎
巨噬细胞
吞噬作用
基因剔除小鼠
细胞生物学
化学
生物
巨噬细胞集落刺激因子
免疫学
癌症研究
受体
医学
生物化学
内科学
体外
作者
Wenqiang Song,Linfeng Liu,Liang Hao,Hao Cheng,Weiyang He,Qianqian Yin,Qian Zhang,Weimin Lin,Hailiang Li,Qijie Li,Wei Liu,Dong Zhang,Dongying Chen,Quan Yuan
标识
DOI:10.1177/00220345241271078
摘要
N6,2′-O-dimethyladenosine (m 6 Am), a common mRNA modification in eukaryotic capped mRNAs, plays a pivotal role in cellular functions and disease progression. However, its involvement in host inflammation remains elusive. Here, we demonstrate that loss of m 6 Am methyltransferase phosphorylated CTD interacting factor 1 (PCIF1) attenuates periodontal inflammation in whole-body and myeloid lineage–specific knockout mouse models. Pcif1 deletion inhibits macrophage phagocytosis and migration through m 6 Am-Csf1r signaling. In addition, colony-stimulating factor-1 receptor (CSF1R) is identified as a potential target for the treatment of periodontitis. We thus reveal a previously unrecognized role for PCIF1-mediated m 6 Am modification in governing macrophage responses and periodontal inflammation.
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