Andrews N W
Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510-8056, USA.
Biol Res. 1993;26(1-2):65-7.
Trypanosoma cruzi invades a wide variety of vertebrate cells by a mechanism distinct from phagocytosis, that involves recruitment and fusion of lysosomes at the site of invasion. A trans-sialidase present on the surface of the trypomastigote forms is capable of removing sialic acid from lgps, major glycoproteins from host cell lysosomes. Lack of sialic acid on lgps facilitates membrane lysis by a parasite-secreted molecule, Tc-TOX, which has membrane pore-forming activity at acidic pH. We propose a sequential model in which these trypanosome products would promote parasite entry into host cells and their subsequent liberation into the cytosol.
克氏锥虫通过一种不同于吞噬作用的机制侵入多种脊椎动物细胞,该机制涉及溶酶体在入侵部位的募集和融合。存在于锥鞭毛体形式表面的转唾液酸酶能够从lgps(宿主细胞溶酶体中的主要糖蛋白)中去除唾液酸。lgps上缺乏唾液酸有利于寄生虫分泌的分子Tc-TOX引起膜裂解,Tc-TOX在酸性pH下具有形成膜孔的活性。我们提出了一个顺序模型,其中这些锥虫产物将促进寄生虫进入宿主细胞并随后释放到细胞质中。