Pron B, Boumaila C, Jaubert F, Berche P, Milon G, Geissmann F, Gaillard J L
Institut National de la Santé et de la Recherche Médicale U 411, 75015 Paris, France.
Cell Microbiol. 2001 May;3(5):331-40. doi: 10.1046/j.1462-5822.2001.00120.x.
We studied the sequence of cellular events leading to the dissemination of Listeria monocytogenes from the gut to draining mesenteric lymph nodes (MLNs) by confocal microscopy of immunostained tissue sections from a rat ligated ileal loop system. OX-62-positive cells beneath the epithelial lining of Peyer's patches (PPs) were the first Listeria targets identified after intestinal inoculation. These cells had other features typical of dendritic cells (DCs): they were large, pleiomorphic and major histocompatibility complex class II(hi). Listeria were detected by microscopy in draining MLNs as early as 6 h after inoculation. Some 80-90% of bacteria were located in the deep paracortical regions, and 100% of the bacteria were present in OX-62-positive cells. Most infected cells contained more than five bacteria each, suggesting that they had arrived already loaded with bacteria. At later stages, the bacteria in these areas were mostly present in ED1-positive mononuclear phagocytes. These cells were also infected by an actA mutant defective in cell-to-cell spreading. This suggests that Listeria are transported by DCs from PPs to the deep paracortical regions of draining MLNs and are then transmitted to other cell populations by mechanisms independent of ActA. Another pathway of dissemination to MLNs was identified, probably involving free Listeria and leading to the infection of ED3-positive mononuclear phagocytes in the subcapsular sinus and adjacent paracortical areas. This study provides evidence that DCs are major cellular targets of L. monocytogenes in PPs and that DCs may be involved in the early dissemination of this pathogen. DCs were not sites of active bacterial replication, making these cells ideal vectors of infection.
我们通过对大鼠结扎回肠袢系统免疫染色组织切片进行共聚焦显微镜检查,研究了导致单核细胞增生李斯特菌从肠道扩散至引流肠系膜淋巴结(MLN)的细胞事件序列。接种肠道后,派尔集合淋巴结(PP)上皮衬里下方的OX-62阳性细胞是首个被鉴定出的李斯特菌靶细胞。这些细胞具有树突状细胞(DC)的其他典型特征:它们体积大、形态多样且主要组织相容性复合体II类呈高表达。接种后6小时,通过显微镜在引流的MLN中检测到李斯特菌。约80%-90%的细菌位于深层副皮质区,且100%的细菌存在于OX-62阳性细胞中。大多数受感染细胞每个都含有超过5个细菌,这表明它们在到达时就已携带细菌。在后期,这些区域的细菌大多存在于ED1阳性单核吞噬细胞中。这些细胞也被细胞间传播缺陷的actA突变体感染。这表明李斯特菌由DC从PP转运至引流MLN的深层副皮质区,然后通过独立于ActA的机制传播至其他细胞群体。还确定了另一条扩散至MLN的途径,可能涉及游离的李斯特菌,并导致被膜下窦和相邻副皮质区的ED3阳性单核吞噬细胞感染。本研究提供了证据,表明DC是PP中单核细胞增生李斯特菌的主要细胞靶标,且DC可能参与该病原体的早期扩散。DC不是活跃细菌复制的场所,使这些细胞成为理想的感染载体。