Galectin-1 蛋白對小菜蛾毒性機制之研究;Characterization of the insecticidal activity of galectin-1 on Plutella xylostella

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题名:	Galectin-1 蛋白對小菜蛾毒性機制之研究;Characterization of the insecticidal activity of galectin-1 on Plutella xylostella
作者:	陳念廷;Nien-Ting Chen
贡献者:	生命科學研究所
关键词:	小菜蛾;幾丁質;蛋白質;protein(galectin-1);Plutella xylostella;chitin
日期:	2005-07-11
上传时间:	2009-09-22 10:19:00 (UTC+8)
出版者:	國立中央大學圖書館
摘要:	摘要 GAL1是ㄧ種動物性半乳糖結合蛋白( Glaectin)，具有多重功能，包括細胞貼附、增生、分化及免疫調節之功能。GAL1 蛋白於細胞質合成後，分泌至細胞外，再與細胞膜上含 β-galactosyl 之蛋白進行結合，進而引發細胞內之訊息傳遞。實驗室先前的研究已證實GAL1蛋白可吸附在幾丁質聚醣膜上，而造成3T3細胞之增生。此外實驗也證實GAL1蛋白能與幾丁聚醣做結合。幾丁質是自然界中最重要的天然聚合物之一，也是昆蟲外胚層衍生構造之胞外基質, 如：外骨骼及腸道外基質(matrix)主要成分。因此本研究擬探討GAL1蛋白對昆蟲生長發育之影響及其毒性作用之機制。結果顯示以GAL1蛋白萃取液或純化之GAL1蛋白餵食三到四齡小菜蛾，可以干擾其正常生長發育；組織切片結果顯示，隨著GAL1劑量增加或處理時間延長，小菜蛾之腸道結構破壞越深。此一結果顯示，GAL1蛋白對小菜蛾之毒性作用可能與腸道組織之破壞有關。實驗結果也顯示幾丁質分解酵素(chitinase)之活性及幾丁質合成酵素(chitin synthase)之表現可被GAL1蛋白所抑制。GAL1與哺乳動物細胞膜蛋白結合的 motif 主要具有Galβ1-4GlcNAc 結構，與幾丁質(β-1,4 N-acetyl-D-glucosamine) 結構相似。因此推測，GAL1對小菜蛾之毒性機制可能與幾丁質產生結合作用，而造成昆蟲幾丁質代謝干擾，進而影響其正常發育。由本實驗結果顯示，GAL1蛋白可以抑制小菜蛾幼蟲正常發育，並具有發展成為生物性殺蟲劑之潛力。 Abstract Galectin-1 (GAL1), a β-galactosyl lectins, has been shown to modulate cell adhesion, cell-matrix interaction, cell proliferation and some immune functions. GAL1 is an extracellular protein acted to cross-linking cell surface and substrate glycoconjugate. Previous work in this laboratory have showed that GAL1-coated chitosan membrane support 3T3 cell proliferation and GAL1 could dose-dependently bind with chitosan (a partial de-acetylated chitin) in vitro. These results suggested that chitosan and chitin could be a natural ligand of GAL1. Chitin is one of the most important biopolymer in nature. In insect, it functions as scaffold materials, supporting the cuticles of the epidermis and trachea as well as peritrophic matrices lining the gut epithelium. In this study, we investigated the effect of GAL1 on insect larval development and the mechanism of its insecticidal activity. The results showed that GAL1 is toxic to the Lepidoptera of Plutella xylostella. The development of third to fourth instar of P. xylostella were significantly disturbed after feeding with GAL1 extract and/or recombinant proteins purified from E.coli-over-expressed GAL1. Histological study showed that midgut of P. xylostella larva was dose-, and time-dependently destroyed after feeding with GAL1. Moreover, the expressions of chitinase activity and PxCS (P. xylostella chitin synthase) were down-regulated by the treatment of GAL1. These results suggested that insecticidal activity of GAL1 toward P. xylostella results from the disruption of midgut integrity. In view of GAL1 having a single carbohydrate-recognition domain recognized the structural motif Galβ1-4GlcNAc that is similar to that of chitosan membrane (?-1,4 N-acetyl-D-glucosamine). We proposed that insecticidal mechanism of GAL1 involves direct binding with chitin. The present study also indicated that GAL1 could be a candidate for bio-insecticide due to its high insecticidal activity.
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