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Molecular characterization, immune functions and DNA protective effects of peroxiredoxin-1 gene in Antheraea pernyi.
Abbas, Muhammad Nadeem; Gul, Isma; Khosravi, Zahra; Amarchi, Jemirade Ifejola; Ye, Xiang; Yu, Lang; Siyuan, Wu; Cui, Hongjuan.
Afiliação
  • Abbas MN; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Gul I; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Khosravi Z; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Amarchi JI; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Ye X; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Yu L; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Siyuan W; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China.
  • Cui H; State Key Laboratory of Resource insects, Southwest University, Chongqing 400716, China; Jinfeng Laboratory, Chongqing 401329, China; Chongqing engineering and Technology Research Center for Silk Biomaterials and Regenerative medicine, Chongqing 400716, China. Electronic address: hcui@swu.edu.cn.
Mol Immunol ; 170: 76-87, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38640818
ABSTRACT
Peroxiredoxins are antioxidant proteins that detoxify peroxynitrite, hydrogen peroxide, and organic hydroperoxides, impacting various physiological processes such as immune responses, apoptosis, cellular homeostasis, and so on. In the present study, we identified and characterized peroxiredoxin 1 from Antheraea pernyi (thereafter designated as ApPrx-1) that encodes a predicted 195 amino acid residue protein with a 21.8 kDa molecular weight. Quantitative real-time PCR analysis revealed that the mRNA level of ApPrx-1 was highest in the hemocyte, fat body, and midgut. Immune-challenged larval fat bodies and hemocytes showed increased ApPrx-1 transcript. Moreover, ApPrx-1 expression was induced in hemocytes and the whole body of A. pernyi following exogenous H2O2 administration. A DNA cleavage assay performed using recombinant ApPrx-1 protein showed that rApPrx-1 protein manifests the ability to protect supercoiled DNA damage from oxidative stress. To test the rApPrx-1 protein antioxidant activity, the ability of the rApPrx-1 protein to remove H2O2 was assessed in vitro using rApPrx-1 protein and DTT, while BSA + DDT served as a control group. The results revealed that ApPrx-1 can efficiently remove H2O2 in vitro. In the loss of function analysis, we found that ApPrx-1 significantly increased the levels of H2O2 in ApPrx-1-depleted larvae compared to the control group. We also found a significantly lower survival rate in the larvae in which ApPrx-1 was knocked down. Interestingly, the antibacterial activity was significantly higher in the ApPrx-1 depleted larvae, compared to the control. Collectively, evidence strongly suggests that ApPrx-1 may regulate physiological activities and provides a reference for further studies to validate the utility of the key genes involved in reliving oxidative stress conditions and regulating the immune responses of insects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Oxidativo / Peroxirredoxinas / Hemócitos / Mariposas Limite: Animals Idioma: En Revista: Mol Immunol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estresse Oxidativo / Peroxirredoxinas / Hemócitos / Mariposas Limite: Animals Idioma: En Revista: Mol Immunol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido