Desjardins M, Descoteaux A
Département de Pathologie et Biologie cellulaire, Université de Montréal, Canada.
Res Immunol. 1998 Sep-Oct;149(7-8):689-92. doi: 10.1016/s0923-2494(99)80040-6.
Microbes have evolved a variety of strategies to survive inside their host cells. Some have the molecular machinery to survive in the hostile environment of phagolysosomes; others escape the phagosome to the more cozy environment of the cell cytoplasm; others inhibit the phagosome fusion with hydrolase-enriched endocytic organelles. This is the case for the promastigote form of the protozoan parasite Leishmania donovani which resides in a phagosome displaying poor fusogenic properties towards endosomes and lysosomes. Recent results indicate that the lipophosphoglycan (LPG), the major cell surface molecule of Leishmania, is involved in the inhibition of phagosome maturation. Further studies in our laboratories are addressing the molecular mechanisms of action of LPG to modulate phagosome fusion properties and its effect on the biogenesis of phagolysosomes.
微生物已经进化出多种策略以在宿主细胞内生存。一些微生物拥有在吞噬溶酶体的恶劣环境中生存的分子机制;另一些则从吞噬体逃逸到细胞质这个更适宜的环境中;还有一些会抑制吞噬体与富含水解酶的内吞细胞器融合。原生动物寄生虫杜氏利什曼原虫的前鞭毛体形式就是如此,它存在于一个对内涵体和溶酶体显示出较差融合特性的吞噬体内。最近的研究结果表明,利什曼原虫的主要细胞表面分子脂磷壁酸(LPG)参与了对吞噬体成熟的抑制作用。我们实验室的进一步研究正在探讨LPG调节吞噬体融合特性的作用分子机制及其对吞噬溶酶体生物发生的影响。