Persat F, Diana J, Benadiba C, Ferrandiz J, Péguet-Navarro J, Peyron F, Picot S, Schmitt D, Vincent C
Laboratoire de Parasitologie, Mycologie Médicale et Pathologie Exotique, Université Claude Bernard, Lyon 1, EA 37-32, 8 Avenue Rockefeller, 69373 Lyon Cedex 08, France.
Exp Parasitol. 2007 Jan;115(1):103-6. doi: 10.1016/j.exppara.2006.06.003. Epub 2006 Aug 4.
Human dendritic cells (DC) obtained in vitro from CD34(+) progenitors (CD34-DC) or blood monocytes (mo-DC) are different DC which may be used in a model of T. gondii infection. We compared the survival, infection rate and cell surface receptor expression of both DC types after living T. gondii tachyzoite infection. CD34-DC appeared less resistant to the parasite than mo-DC. At 48h post-infection, chemokine receptors responsible for DC homing and migration were absent in mo-DC, while down regulation of CCR6 and up regulation of CCR7 was observed in CD34-DC. This result, suggesting migration ability of CD34-DC, was confirmed by in vitro migration experiments against different chemokines. Tachyzoite supernatant, used as chemokine, attracted immature CD34-DC as observed by MIP3alpha, while MIP3beta, as expected, attracted mature CD34-DC. Under similar conditions, no significant difference was noticed between mature or immature mo-DC. These data indicated that CD34-DC represent an alternative model that allows migration assay of infected DC by T. gondii.
从CD34(+)祖细胞(CD34-DC)或血液单核细胞(mo-DC)体外获得的人树突状细胞(DC)是不同的DC类型,可用于弓形虫感染模型。我们比较了活的弓形虫速殖子感染后两种DC类型的存活率、感染率和细胞表面受体表达。CD34-DC对寄生虫的抵抗力似乎比mo-DC弱。感染后48小时,mo-DC中负责DC归巢和迁移的趋化因子受体缺失,而在CD34-DC中观察到CCR6下调和CCR7上调。这一表明CD34-DC迁移能力的结果通过针对不同趋化因子的体外迁移实验得到了证实。作为趋化因子使用的速殖子上清液,如MIP3α所示,吸引未成熟的CD34-DC,而正如预期的那样,MIP3β吸引成熟的CD34-DC。在类似条件下,成熟或未成熟的mo-DC之间未发现显著差异。这些数据表明,CD34-DC代表了一种替代模型,可用于对弓形虫感染的DC进行迁移分析。