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.
Garg, S., Volpe, E., Palmieri, G., Mattei, M., Galati, D., Martino, A.m., et al. (2004). Sphingosine 1-phosphate induces antimicrobial activity both in vitro and in vivo. THE JOURNAL OF INFECTIOUS DISEASES, 189(11), 2129-2138 [10.1086/386286].
Sphingosine 1-phosphate induces antimicrobial activity both in vitro and in vivo
PALMIERI, GIAMPIERO;MATTEI, MAURIZIO;BONANNO, ELENA;DE VITO, PAOLO;SPAGNOLI, LUIGI GIUSTO;COLIZZI, VITTORIO;FRAZIANO, MAURIZIO
2004-06-01
Abstract
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.