Berasaín P, Goñi F, McGonigle S, Dowd A, Dalton J P, Frangione B, Carmona C
Unidad de Biologia Parasitaria, Instituto de Higiene, Montevideo, Uruguay.
J Parasitol. 1997 Feb;83(1):1-5.
The invasive stages of the parasitic trematode Fasciola hepatica release proteinases into the medium in which they are maintained. In this study, we investigated the interaction of F. hepatica excretory/secretory (E/S) products and 2 cysteine proteinases (CL1 and CL2) purified from these products with extracellular matrix and basement membrane macromolecules. Fasciola hepatica E/S products contained collagenolytic activity on fibrillar types I and III collagen as well as basement membrane type IV collagen. CL1 and CL2 were capable of degrading acid-soluble type III and type IV collagen but not insoluble type I collagen. In contrast, neither the E/S products nor the purified CL1 and CL2 showed elastinolytic activity. Fibronectin and laminin were degraded by E/S products and by CL1 and CL2. Sequence analysis of fibronectin degradation products showed that the fragments obtained corresponded to complete biologically active domains. These results indicate that the cysteine proteinases secreted by F. hepatica may be involved in the process of tissue invasion by the parasite.
寄生吸虫肝片吸虫的侵入阶段会向其生存的培养基中释放蛋白酶。在本研究中,我们调查了肝片吸虫排泄/分泌(E/S)产物以及从这些产物中纯化出的两种半胱氨酸蛋白酶(CL1和CL2)与细胞外基质和基底膜大分子之间的相互作用。肝片吸虫E/S产物对I型和III型纤维状胶原蛋白以及基底膜IV型胶原蛋白具有胶原olytic活性。CL1和CL2能够降解酸溶性III型和IV型胶原蛋白,但不能降解不溶性I型胶原蛋白。相比之下,E/S产物以及纯化的CL1和CL2均未表现出弹性蛋白分解活性。纤连蛋白和层粘连蛋白被E/S产物以及CL1和CL2降解。纤连蛋白降解产物的序列分析表明,获得的片段对应于完整的生物活性结构域。这些结果表明,肝片吸虫分泌的半胱氨酸蛋白酶可能参与了该寄生虫的组织侵入过程。