Garg Sanjay K, Volpe Elisabetta, Palmieri Graziana, Mattei Maurizio, Galati Domenico, Martino Angelo, Piccioni Maria S, Valente Emanuela, Bonanno Elena, De Vito Paolo, Baldini Patrizia M, Spagnoli Luigi G, Colizzi Vittorio, Fraziano Maurizio
Department of Biology, University of Tor Vergata, Rome, Italy.
J Infect Dis. 2004 Jun 1;189(11):2129-38. doi: 10.1086/386286. Epub 2004 May 10.
Sphingosine 1-phosphate (S1P), a polar sphingolipid metabolite, is involved in a wide spectrum of biological processes, including Ca(++) mobilization, cell growth, differentiation, motility, and cytoskeleton organization. Here, we show a novel role of S1P in the induction of antimicrobial activity in human macrophages that leads to the intracellular killing of nonpathogenic Mycobacterium smegmatis and pathogenic M. tuberculosis. Such activity is mediated by host phospholipase D, which favors the acidification of mycobacteria-containing phagosomes. Moreover, when it was intravenously injected in mycobacteria-infected mice, S1P reduced mycobacterial growth and pulmonary tissue damage. These results identify S1P as a novel regulator of the host antimicrobial effector pathways.
鞘氨醇-1-磷酸(S1P)是一种极性鞘脂代谢产物,参与多种生物学过程,包括钙离子动员、细胞生长、分化、运动及细胞骨架组织。在此,我们展示了S1P在诱导人类巨噬细胞抗菌活性中的新作用,该活性导致对非致病性耻垢分枝杆菌和致病性结核分枝杆菌的细胞内杀伤。这种活性由宿主磷脂酶D介导,其有利于含分枝杆菌吞噬体的酸化。此外,当将S1P静脉注射到分枝杆菌感染的小鼠体内时,它可减少分枝杆菌生长及肺组织损伤。这些结果表明S1P是宿主抗菌效应途径的新型调节因子。