吞噬细胞
吞噬作用
生物
免疫学
细胞生物学
单核吞噬细胞系统
巨噬细胞
炎症
免疫系统
先天免疫系统
作者
James J. Phelan,Frederick J. Sheedy
标识
DOI:10.1016/j.it.2021.08.011
摘要
Selectively targeting facets of neutrophil function could benefit infectious and inflammatory diseases. Amara et al. report on a compound which blocks human neutrophil activation by activating the glycolytic enzyme phosphofructokinase, liver-type (PFKL). Altering glucose fate by modulating this key enzymatic step could dramatically alter the function and fate of phagocytes.
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