{"title":"类似 Galectin-8 的异构体 X1 通过积极调节促炎细胞因子、趋化因子和酶的抗氧化活性,介导红唇鲻鱼(Planiliza haematocheilus)的抗菌、抗病毒和抗氧化反应","authors":"W.A.D.L.R. Warnakula , H.M.V. Udayantha , D.S. Liyanage , E.M.T. Tharanga , W.K.M. Omeka , M.A.H. Dilshan , H.A.C.R. Hanchapola , J.D.H.E. Jayasinghe , Taehyug Jeong , Qiang Wan , Jehee Lee","doi":"10.1016/j.dci.2024.105182","DOIUrl":null,"url":null,"abstract":"<div><p>Galectin 8 belongs to the tandem repeat subclass of the galectin superfamily. It possesses two homologous carbohydrate recognition domains linked by a short peptide and preferentially binds to β-galactoside-containing glycol-conjugates in a calcium-independent manner. This study identified Galectin-8-like isoform X1 (<em>PhGal8X1</em>) from red-lip mullet (<em>Planiliza haematocheilus</em>) and investigated its role in regulating fish immunity. The open reading frame of <em>PhGal8X1</em> was 918bp, encoding a soluble protein of 305 amino acids. The protein had a theoretical isoelectric (pI) point of 7.7 and an estimated molecular weight of 34.078 kDa. <em>PhGal8X1</em> was expressed in various tissues of the fish, with prominent levels in the brain, stomach, and intestine. <em>PhGal8X1</em> expression was significantly (<em>p</em> < 0.05) induced in the blood and spleen upon challenge with different immune stimuli, including polyinosinic:polycytidylic acid, lipopolysaccharide, and <em>Lactococcus garvieae</em>. The recombinant PhGal8X1 protein demonstrated agglutination activity towards various bacterial pathogens at a minimum effective concentration of 50 μg/mL or 100 μg/mL. Subcellular localization observations revealed that PhGal8X1 was primarily localized in the cytoplasm. <em>PhGal8X1</em> overexpression in fathead minnow cells significantly (<em>p</em> < 0.05) inhibited viral hemorrhagic septicemia virus (VHSV) replication. The expression levels of four proinflammatory cytokines and two chemokines were significantly (<em>p</em> < 0.05) upregulated in <em>PhGal8X1</em> overexpressing cells in response to VHSV infection. Furthermore, overexpression of <em>PhGal8X1</em> exhibited protective effects against oxidative stress induced by H<sub>2</sub>O<sub>2</sub> through the upregulation of antioxidant enzymes. Taken together, these findings provide compelling evidence that <em>PhGal8X1</em> plays a crucial role in enhancing innate immunity and promoting cell survival through effective regulation of antibacterial, antiviral, and antioxidant defense mechanisms in red-lip mullet.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Galectin-8-like isoform X1 mediates antibacterial, antiviral, and antioxidant responses in red-lip mullet (Planiliza haematocheilus) through positive modulation of pro-inflammatory cytokine, chemokine, and enzymatic antioxidant activity\",\"authors\":\"W.A.D.L.R. Warnakula , H.M.V. Udayantha , D.S. Liyanage , E.M.T. Tharanga , W.K.M. Omeka , M.A.H. Dilshan , H.A.C.R. Hanchapola , J.D.H.E. Jayasinghe , Taehyug Jeong , Qiang Wan , Jehee Lee\",\"doi\":\"10.1016/j.dci.2024.105182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Galectin 8 belongs to the tandem repeat subclass of the galectin superfamily. It possesses two homologous carbohydrate recognition domains linked by a short peptide and preferentially binds to β-galactoside-containing glycol-conjugates in a calcium-independent manner. This study identified Galectin-8-like isoform X1 (<em>PhGal8X1</em>) from red-lip mullet (<em>Planiliza haematocheilus</em>) and investigated its role in regulating fish immunity. The open reading frame of <em>PhGal8X1</em> was 918bp, encoding a soluble protein of 305 amino acids. The protein had a theoretical isoelectric (pI) point of 7.7 and an estimated molecular weight of 34.078 kDa. <em>PhGal8X1</em> was expressed in various tissues of the fish, with prominent levels in the brain, stomach, and intestine. <em>PhGal8X1</em> expression was significantly (<em>p</em> < 0.05) induced in the blood and spleen upon challenge with different immune stimuli, including polyinosinic:polycytidylic acid, lipopolysaccharide, and <em>Lactococcus garvieae</em>. The recombinant PhGal8X1 protein demonstrated agglutination activity towards various bacterial pathogens at a minimum effective concentration of 50 μg/mL or 100 μg/mL. Subcellular localization observations revealed that PhGal8X1 was primarily localized in the cytoplasm. <em>PhGal8X1</em> overexpression in fathead minnow cells significantly (<em>p</em> < 0.05) inhibited viral hemorrhagic septicemia virus (VHSV) replication. The expression levels of four proinflammatory cytokines and two chemokines were significantly (<em>p</em> < 0.05) upregulated in <em>PhGal8X1</em> overexpressing cells in response to VHSV infection. Furthermore, overexpression of <em>PhGal8X1</em> exhibited protective effects against oxidative stress induced by H<sub>2</sub>O<sub>2</sub> through the upregulation of antioxidant enzymes. Taken together, these findings provide compelling evidence that <em>PhGal8X1</em> plays a crucial role in enhancing innate immunity and promoting cell survival through effective regulation of antibacterial, antiviral, and antioxidant defense mechanisms in red-lip mullet.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-04-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0145305X24000545\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0145305X24000545","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Galectin-8-like isoform X1 mediates antibacterial, antiviral, and antioxidant responses in red-lip mullet (Planiliza haematocheilus) through positive modulation of pro-inflammatory cytokine, chemokine, and enzymatic antioxidant activity
Galectin 8 belongs to the tandem repeat subclass of the galectin superfamily. It possesses two homologous carbohydrate recognition domains linked by a short peptide and preferentially binds to β-galactoside-containing glycol-conjugates in a calcium-independent manner. This study identified Galectin-8-like isoform X1 (PhGal8X1) from red-lip mullet (Planiliza haematocheilus) and investigated its role in regulating fish immunity. The open reading frame of PhGal8X1 was 918bp, encoding a soluble protein of 305 amino acids. The protein had a theoretical isoelectric (pI) point of 7.7 and an estimated molecular weight of 34.078 kDa. PhGal8X1 was expressed in various tissues of the fish, with prominent levels in the brain, stomach, and intestine. PhGal8X1 expression was significantly (p < 0.05) induced in the blood and spleen upon challenge with different immune stimuli, including polyinosinic:polycytidylic acid, lipopolysaccharide, and Lactococcus garvieae. The recombinant PhGal8X1 protein demonstrated agglutination activity towards various bacterial pathogens at a minimum effective concentration of 50 μg/mL or 100 μg/mL. Subcellular localization observations revealed that PhGal8X1 was primarily localized in the cytoplasm. PhGal8X1 overexpression in fathead minnow cells significantly (p < 0.05) inhibited viral hemorrhagic septicemia virus (VHSV) replication. The expression levels of four proinflammatory cytokines and two chemokines were significantly (p < 0.05) upregulated in PhGal8X1 overexpressing cells in response to VHSV infection. Furthermore, overexpression of PhGal8X1 exhibited protective effects against oxidative stress induced by H2O2 through the upregulation of antioxidant enzymes. Taken together, these findings provide compelling evidence that PhGal8X1 plays a crucial role in enhancing innate immunity and promoting cell survival through effective regulation of antibacterial, antiviral, and antioxidant defense mechanisms in red-lip mullet.