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Feng Ming Zou,이광식,김보연,김홍자,Zhong Zheng Gui,Guozheng Zhang,Xijie Guo,진병래 한국응용곤충학회 2015 Journal of Asia-Pacific Entomology Vol.18 No.4
Insect cuticular melanization is regulated by the prophenoloxidase (proPO)-activating system, which is also involved in the innate immune reaction. Here, we demonstrate how the differentiation of the proPO-activating system is regulated toward a cuticular melanization or innate immunity function in silkworm (Bombyx mori) pupae. Our results indicate that the differential and spatial regulation of key components, such as the proPOactivating enzyme and proPOs, primes the proPO-activating system for either cuticular melanization or innate immunity. This dual strategy for cuticular melanization in development and innate immunity upon infection demonstrates a two-pronged defense mechanism that is mediated by the priming of the proPO system.
Feng Ming Zou,이광식,Hu Wan,Zhong Zheng Gui,진병래 한국응용곤충학회 2014 Journal of Asia-Pacific Entomology Vol.17 No.1
Insect growth-blocking peptides (GBPs) exhibit growth-blocking and paralytic activity. Low concentrations ofGBP stimulate larval growth, whereas high concentrations of GBP significantly retard larval growth. Here, weshow that morphological abnormalities and lethality were induced in silkworm (Bombyx mori) larvae by highconcentrations of GBP. Active B. mori GBP (BmGBP) was produced by treating recombinant proBmGBP(expressed in baculovirus-infected insect cells) with bovine factor Xa. When silkworm larvae on day 1 of thefifth-instar stage were injected between the seventh and eight abdominal segments with BmGBP (100 or500 ng/larva), the larval–pupal and pupal–adult transformations of these silkworms were delayed in a dosedependentmanner. However, a high concentration (2000 ng/larva) of BmGBP or Spodoptera exigua GBP(SeGBP) acutely induced morphological abnormalities and death in silkworm larvae. In silkwormlarvae treatedwith high concentrations of GBPs, the ingested food excessively accumulated in the foregut, which caused extremeswelling in both the thorax and the foregut and resulted in larval death. Therefore, these results notonly provide insight into the effect of insect GBPs on gut physiology but also reveal a novel function of insectGBPs.
Prophenoloxidase-Activating Factor Involves in the Pupal Melanization of Bombyx mori
Kwang Sik Lee,Feng Ming Zou,Bo Yeon Kim,Byung Rae Jin 한국응용곤충학회 2012 한국응용곤충학회 학술대회논문집 Vol.2012 No.05
In arthropods, an immune challenge triggers a serine protease cascade that leads to the activation of prophenoloxidase (proPO)-activating factors (PPAFs), which are also called proPO-activating enzymes (PPAEs) or proteinases (PAPs). PPAFs are activated by cleavage between their clip and serine protease domains. Once activated, PPAFs convert proPO to phenoloxidase (PO), which then catalyzes the production of quinones to form melanin. In this study, we identified a Bombyx mori PPAF(BmPPAF) that involves in the pupal melanization. In the fat body, expression of BmPPAF was detected on day 1 to 3 of the pupal stage. RNA interference (RNAi)-mediated BmPPAF knock-down inhibited pupal melanization, resulting in the delay of pupal melanization. Based on these results, we concluded that BmPPAF is involved in the melanization of pupal stage in silkworm metamorphosis.
Kwang Sik Lee,Feng Ming Zou,Bo Yeon Kim,Hu Wan,Hyung Joo Yoon,Hong Ja Kim,Sook Jae Seo,Yeon Ho Je,Soo Dong Woo,Byung Rae Jin 한국응용곤충학회 2013 한국응용곤충학회 학술대회논문집 Vol.2013 No.10
Insect cuticular melanization is regulated by the prophenoloxidase (proPO)- activating system, which is also involved in the innate immune reaction. Here, we demonstrate how the differentiation of the proPO-activating system is regulated toward a cuticular melanization or innate immunity function in silkworm (Bombyx mori) pupae. Our results indicate that the differential and spatial regulation of key components, such as the proPO-activating factor, tyrosine hydroxylase, and porPOs, primes the proPO-activating system for either cuticular melanization or innate immunity. This dual strategy for cuticular melanization in development and innate immunity upon infection demonstrates a two-pronged defense mechanism that is mediated by the priming of the proPO system.
Antimicrobial Activity of a Honeybee (Apis cerana) Venom Kazal-Type Serine Protease Inhibitor
Bo Yeon Kim,Kwang Sik Lee,Feng Ming Zou,Hu Wan,Yong Soo Choi,Hyung Joo Yoon,Hyung Wook Kwon,Yeon Ho Je,Byung Rae Jin 한국응용곤충학회 2013 한국응용곤충학회 학술대회논문집 Vol.2013 No.10
Insect-derived Kazal-type serine protease inhibitors exhibit thrombin, elastase, plasmin, proteinase K, or subtilisin A inhibition activity, but so far, no functional roles for bee-derived Kazal-type serine protease inhibitors have been identified. In this study, a bee (Apis cerana) venom Kazal-type serine protease inhibitor (AcKTSPI) that acts as a microbial serine protease inhibitor was identified. AcKTSPI contained a single Kazal domain that displayed six conserved cysteine residues and a P1 threonine residue. AcKTSPI was expressed in the venom gland and was present as a 10-kDa peptide in bee venom. Recombinant AcKTSPI Kazal domain (AcKTSPI-Kd) expressed in baculovirus-infected insect cells demonstrated inhibitory activity against subtilisin A (Ki 67.03 nM) and proteinase K (Ki 91.53 nM), but not against α-chymotrypsin or typsin, which implies a role for AcKTSPI as a microbial serine protease inhibitor. However, AcKTSPI-Kd exhibited no detectable inhibitory effects on factor Xa, thrombin, tissue plasminogen activator, or elastase. Additionally, AcKTSPI-Kd bound directly to Bacillus subtilis, B. thuringiensis, Beauveria bassiana, and Fusarium graminearum but not to Escherichia coli. Consistent with these findings, AcKTSPI-Kd showed antibacterial activity against Gram-positive bacteria and antifungal activity against both plant-pathogenic and entomopathogenic fungi. These findings constitute molecular evidence that AcKTSPI acts as an inhibitor of microbial serine proteases. This paper provides a novel view of the antimicrobial functions of a bee venom Kazal-type serine protease inhibitor.
Zou, Jin-Feng,Xia, Ming-yao Techno-Press 2017 Geomechanics & engineering Vol.12 No.3
The problem of cylindrical cavity expansion incorporating deformation dependent of intermediate principal stress in rock or soil mass is investigated in the paper. Assumptions that the initial axial total strain is a non-zero constant and the axial plastic strain is not zero are defined to obtain the numerical solution of strain which incorporates deformation-dependent intermediate principal stress. The numerical solution of plastic strains are achieved by the 3-D plastic potential functions based on the M-C and generalized H-B failure criteria, respectively. The intermediate principal stress is derived with the Hook's law and plastic strains. Solution of limited expansion pressure, stress and strain during cylindrical cavity expanding are given and the corresponding calculation approaches are also presented, which the axial stress and strain are incorporated. Validation of the proposed approach is conducted by the published results.
( Feng Yao Wu ),( Feng Ming Zou ),( Jun Qiang Jia ),( Sheng Peng Wang ),( Guo Zheng Zhang ),( Xi Jie Guo ),( Zhong Zheng Gui ) 한국잠사학회 2011 International Journal of Industrial Entomology Vol.23 No.1
Cathepsins are well-characterized proteases that are ubiquitously expressed in lysosomes. Previous work revealed that Bombyx mori cathepsins B and D are expressed in the fat body and undergo decomposition during larval-pupal metamorphosis. Quantitative RTPCR was performed to detect cathepsin gene expression at the transcription level when challenged by B. mori nuclear polyhedrosis virus (BmNPV), temperature and hormones (20-hydroxyecdysone (20E) and juvenile hormone analogue (JHA)). mRNAs encoding cathepsins B and D were significantly enhanced after the larvae were infected with BmNPV, and the peak of the induction appeared at 1 day before spinning. This attenuated the inducing effect on cathepsin expression caused by infection. Temperature shock induced cathepsin expression at the later stage of the 5th instar, and transcription levels varied with development stage and temperature. Cathepsin B and D mRNA expression in the fat body were significantly induced by JHA at the day before spinning, and with 20E, the expression reached a peak at the last day of the 5th instar. Cathepsin B and D mRNA expression exhibited detectable changes post-treatment, without significant differences between or among the hormone concentrations.
( Ming Ke Wang ),( Hui Qin Sun ),( Fan Jiang ),( Jing Han ),( Feng Ye ),( Tao Wang ),( Yong Ping Su ),( Zhong Min Zou ) 생화학분자생물학회 (구 한국생화학분자생물학회) 2010 BMB Reports Vol.43 No.12
A novel gene, designated mgt-6, containing four splicing variants, was isolated from a gene trap clone library of C3H/10T1/ 2 cells transfected with retroviral promoterless gene-trap vector, ROSAFARY. The transcript variants were differentially expressed in murine tissues and cell lines and differentially responded to diverse stimuli including TGF-β1 and mitogen-activated protein kinase (MAPK) inhibitors. The mgt-6 gene encoded a protein of 37 or 11 amino acid residuals with cytoplasmic distribution. However, when C3H/10T1/2 cells were treated with 5-azacytidine, the protein translocated into cell nucleus as indicated by fused LacZ or C-terminally tagged EGFP. Our preliminary results suggest that further study on the role of mgt-6 gene in cell transformation and differentiation may be of significance. [BMB reports 2010; 43(12): 789-794]
The Influence of Challenge on Cathepsin B and D Expression Patterns in the Silkworm Bombyx mori L.
Wu, Feng-Yao,Zou, Feng-Ming,Jia, Jun-Qiang,Wang, Sheng-Peng,Zhang, Guo-Zheng,Guo, Xi-Jie,Gui, Zhong-Zheng Korean Society of Sericultural Science 2011 International Journal of Industrial Entomology Vol.23 No.1
Cathepsins are well-characterized proteases that are ubiquitously expressed in lysosomes. Previous work revealed that $Bombyx$ $mori$ cathepsins B and D are expressed in the fat body and undergo decomposition during larval-pupal metamorphosis. Quantitative RT-PCR was performed to detect cathepsin gene expression at the transcription level when challenged by $B.$ $mori$ nuclear polyhedrosis virus (BmNPV), temperature and hormones (20-hydroxyecdysone (20E) and juvenile hormone analogue (JHA)). mRNAs encoding cathepsins B and D were significantly enhanced after the larvae were infected with BmNPV, and the peak of the induction appeared at 1 day before spinning. This attenuated the inducing effect on cathepsin expression caused by infection. Temperature shock induced cathepsin expression at the later stage of the $5^{th}$ instar, and transcription levels varied with development stage and temperature. Cathepsin B and D mRNA expression in the fat body were significantly induced by JHA at the day before spinning, and with 20E, the expression reached a peak at the last day of the $5^{th}$ instar. Cathepsin B and D mRNA expression exhibited detectable changes post-treatment, without significant differences between or among the hormone concentrations.