Peroxinectin, a cell adhesive protein associated with the proPO system from the black tiger shrimp, Penaeus monodon

被引:130
作者
Sritunyalucksana, K
Wongsuebsantati, K
Johansson, MW
Söderhäll, K
机构
[1] Uppsala Univ, Evolut Biol Ctr, Dept Comparat Physiol, SE-75236 Uppsala, Sweden
[2] Mahidol Univ, Fac Sci, Dept Biotechnol, Bangkok 10400, Thailand
[3] Univ Wisconsin, Dept Med, Med Sci Ctr 4285A, Madison, WI 53706 USA
基金
瑞典研究理事会;
关键词
peroxinectin; cell adhesion; peroxidase; Penaeus monodon; the proPO system; integrin binding motif; fungal infection; bacterial infection;
D O I
10.1016/S0145-305X(01)00009-X
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Upon activation of the prophenoloxidase activating system in the shrimp, Penaeus monodon, a cell adhesion activity in the haemolymph is generated. A cell adhesion assay showed that a high number of granular cells (60%) adhered to coverslips coated with a shrimp haemocyte lysate supernatant, whereas a very low number of cells adhered to coverslips coated with bovine serum albumin. Inhibition of adhesion by an antiserum against crayfish peroxinectin, a cell adhesion protein, revealed that the cell adhesion activity detected in shrimp haemocyte lysate supernatant might result from a peroxinectin-like molecule in shrimp. A cDNA clone encoding shrimp peroxinectin was isolated, which had an open reading frame of 2337 nucleotides, with a polyadenylation sequence and a poly A tail. II encodes a protein of 778 amino acids including a 20 amino acid signal peptide. The mature protein (758 amino acids) has a predicted molecular mass of 84.8 kDa and an estimated pi of 9.0. Two putative integrin binding motifs, RGD (Arg-Gly-Asp) and KGD (Lys-Gly-Asp), were found in shrimp peroxinectin. Sequence comparison shows that the shrimp protein is similar to crayfish peroxinectin (69%) and to various peroxidases and putative peroxidases from invertebrates and vertebrates. The shrimp peroxinectin cDNA also shows similarity (51%) to both Drosophila peroxinectin-related protein (AAF78217) and peroxidasin (S46224), an extracellular matrix protein combining an active peroxidase domain as well as immunoglobulin domains, leucine rich repeats and procollagen-like motif. However, the sequence similarity to both Drosophila molecules are mostly within the peroxidase domain. Northern blot analysis, using a non-peroxidase region in peroxinectin as: a probe. revealed that peroxinectin is constitutively expressed in shrimp haemocyte and was reduced significantly in shrimp injected with a beta -1,3-glucan,laminarin, to mimic an infection with a fungus. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:353 / 363
页数:11
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