转录组
生物
免疫学
流式细胞术
背景(考古学)
人口
电池类型
疾病
基因
医学
细胞
病理
基因表达
遗传学
古生物学
环境卫生
作者
Xiaolin Zhang,Guiqin He,Yixuan Hu,Boren Liu,Xu Yuliang,Xia Li,Xinyou Lv,Jin Li
标识
DOI:10.1186/s12979-024-00448-x
摘要
Abstract Background Neutrophils play an essential role in Alzheimer’s disease (AD) pathology. However, the extent of their heterogeneity remains poorly explored, particularly in the context of developing novel therapies targeting these cells. Results We investigate the population structure of neutrophils purified from peripheral blood samples of AD mice. Utilizing single cell RNA sequencing, we comprehensively map neutrophil populations into six distinct clusters and find that the Neu-5 subset is specially enriched in AD mice. This subset exhibits fewer specific granules and a lower mature score. Gene ontology (GO) analysis reveals that genes involved in cytokine-mediated signaling are downregulated in the Neu-5 cluster. Furthermore, we identify the Ccrl2 gene is specifically upregulated in this subgroup, which is confirmed by flow cytometry in AD mice. Finally, immunohistochemical staining indicates that CCRL2 protein is increased in the brains of AD mice. Conclusions We identify a unique CCRL2 positive neutrophil cluster, that is specifically enriched in the peripheral blood of AD mice.
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