作者: Javier Pizarro-Cerda , Jean-Pierre Gorvel , Edgardo Moreno , Claire Forestier
DOI:
关键词: In vivo 、 Internalization 、 Cell biology 、 Extracellular 、 Biology 、 In vitro 、 Intracellular 、 Peritoneal cavity 、 Endosome 、 Lipopolysaccharide
摘要: In this study, we detailed in a time-dependent manner the trafficking, recycling, and structural fate of Brucella abortus LPS murine peritoneal macrophages by immunofluorescence, ELISA, biochemical analyses. The intracellular pathway B. LPS, nonclassical endotoxin, was investigated both vivo after injection cavity mice vitro incubation with macrophages. We also followed trafficking infection strain 19. After binding to cell surface internalization, is routed from early endosomes lysosomes unusual slow kinetics. It accumulates there for at least 24 h. Later, leaves reaches macrophage surface. This recycling observed released S19 following infection. Indeed, 72 h postinfection, bacteria are degraded located inside dispersed periphery. From onward, gradually detected plasma membrane. each case, present found large clusters O-chain facing extracellular medium. Both antigenicity heterogenicity moiety preserved during trafficking. demonstrate that not cleared either or 3 mo, exposing its immunogenic toward