Dowdell Alexander S, Colgan Sean P
Mucosal Inflammation Program and Division of Gastroenterology and Hepatology, Department of Medicine, University of Colorado, Aurora, CO, USA.
Department of Medicine, Rocky Mountain Veterans Regional VA Medical Center, Aurora, CO, USA.
Immunometabolism (Cobham). 2025 Jul 21;7(3):e00067. doi: 10.1097/IN9.0000000000000067. eCollection 2025 Jul.
In a recent publication, Lesbats et al uncover the molecular fate of phagocytosed bacterial contents. The authors observed incorporation of bacterial biomolecules (amino acids, metabolites) into those of the host macrophage through stable isotope labeling and mass spectrometry. Further, the authors found that the state of the phagocytosed bacteria, living or dead, dramatically alters the macrophage's metabolic program toward either a pro-inflammatory or a "recycling" direction, respectively. This commentary summarizes these findings and further discusses the implications of this work in a broader sense.
在最近的一篇出版物中,莱斯巴茨等人揭示了被吞噬细菌内容物的分子命运。作者通过稳定同位素标记和质谱法观察到细菌生物分子(氨基酸、代谢物)掺入宿主巨噬细胞的生物分子中。此外,作者发现被吞噬细菌的状态,即活的或死的,会分别使巨噬细胞的代谢程序朝着促炎或“回收利用”方向发生显著改变。本评论总结了这些发现,并从更广泛的意义上进一步讨论了这项工作的意义。