Enzymology of the nematode cuticle: A potential drug target?

被引:90
作者
Page, Antony P. [1 ]
Stepek, Gillian [1 ]
Winter, Alan D. [1 ]
Pertab, David [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Inst Biodivers Anim Hlth & Comparat Med, Glasgow G61 1QH, Lanark, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Nematode; Cuticle; Collagen; Moulting; Ecdysis; Protease; C; elegans; PLANT CYSTEINE PROTEINASES; RODENT GASTROINTESTINAL NEMATODE; CAENORHABDITIS-ELEGANS CUTICLE; CROSS-LINKING ACTIVITY; IN-VITRO DEVELOPMENT; EXTRACELLULAR-MATRIX; PROLYL; 4-HYDROXYLASE; ANCYLOSTOMA-CANINUM; DIROFILARIA-IMMITIS; ONCHOCERCA-VOLVULUS;
D O I
10.1016/j.ijpddr.2014.05.003
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
All nematodes possess an external structure known as the cuticle, which is crucial for their development and survival. This structure is composed primarily of collagen, which is secreted from the underlying hypodermal cells. Extensive studies using the free-living nematode Caenorhabditis elegans demonstrate that formation of the cuticle requires the activity of an extensive range of enzymes. Enzymes are required both pre-secretion, for synthesis of component proteins such as collagen, and post-secretion, for removal of the previous developmental stage cuticle, in a process known as moulting or exsheathment. The excretion/secretion products of numerous parasitic nematodes contain metallo-, serine and cysteine proteases, and these proteases are conserved across the nematode phylum and many are involved in the moulting/exsheathment process. This review highlights the enzymes required for cuticle formation, with a focus on the post-secretion moulting events. Where orthologues of the C. elegans enzymes have been identified in parasitic nematodes these may represent novel candidate targets for future drug/vaccine development. (C) 2014 Published by Elsevier Ltd. on behalf of Australian Society for Parasitology Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
引用
收藏
页码:133 / 141
页数:9
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