Sampaio Weverton M, Moura Eliane P, Arruda Felipe C S, Ribeiro Raul R, Alves Cíntia F, Melo Ferdinan A, Fernandes Ana Paula S M, Michalick Marilene S M, Melo Maria N, Tafuri Washington L, Tafuri Wagner L
Departamento de Patologia Geral, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
BMC Vet Res. 2007 May 30;3:11. doi: 10.1186/1746-6148-3-11.
There are a few works considering the characterization of canine monocyte-derived macrophages as well as a standardized procedure for isolation, culture, and infection of these cells with Leishmania. We have performed several modifications in order to improve the canine monocyte-derived macrophage cultures. In addition, we have done a comparative study between monocytes and monocyte-derived macrophages from dogs naturally and experimentally infected with L. chagasi.
In the presence of exogenous serum, opsonized Leishmania promastigotes binds better to monocytes/macrophages than without serum. Otherwise, this binding occurs due to the strict correlation between the opsonized biologic particles with the third receptor of the complement (CR3-CD11b/CD18). In fact, our assays with CD11b confirmed the importance of this receptor for canine cells and the L. chagasi experimental system. Moreover, monocytes obtained from naturally infected dogs have shown a higher number of monocytes bounded to promastigotes. The experimental results regarding survival have shown that promastigote forms of opsonized L. chagasi were more infective, because we found higher numbers of promastigotes bound to the different cells. As a consequence, after forty-eight hours of binding, higher numbers of amastigotes appeared inside monocyte-macrophages.
These studies have given support to continue comparative studies involving canine monocytes, monocyte-derived macrophages and peritoneal macrophages. Since we have standardized the canine cell culture, we are looking forward to determining the phenotypic properties of these cells before and after L. chagasi infection using flow cytometry.
有一些研究考虑了犬单核细胞衍生巨噬细胞的特性以及这些细胞与利什曼原虫分离、培养和感染的标准化程序。我们进行了一些改进,以优化犬单核细胞衍生巨噬细胞的培养。此外,我们对自然感染和实验感染恰加斯利什曼原虫的犬的单核细胞和单核细胞衍生巨噬细胞进行了比较研究。
在外源血清存在的情况下,调理过的利什曼原虫前鞭毛体比无血清时更易与单核细胞/巨噬细胞结合。此外,这种结合是由于调理过的生物颗粒与补体的第三受体(CR3-CD11b/CD18)之间的严格相关性。事实上,我们用CD11b进行的试验证实了该受体对犬细胞和恰加斯利什曼原虫实验系统的重要性。此外,从自然感染犬获得的单核细胞显示出与前鞭毛体结合的单核细胞数量更多。关于存活的实验结果表明,调理过的恰加斯利什曼原虫前鞭毛体形式更具感染性,因为我们发现与不同细胞结合的前鞭毛体数量更多。因此,结合48小时后,单核细胞-巨噬细胞内出现了更多的无鞭毛体。
这些研究为继续开展涉及犬单核细胞、单核细胞衍生巨噬细胞和腹膜巨噬细胞的比较研究提供了支持。由于我们已经对犬细胞培养进行了标准化,我们期待使用流式细胞术确定恰加斯利什曼原虫感染前后这些细胞的表型特性。