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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Protective Function of Novel Fungal Immunomodulatory Proteins Fip-lti1 and Fip-lti2 from Lentinus tigrinus in Concanavalin A-Induced Liver Oxidative Injury
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Protective Function of Novel Fungal Immunomodulatory Proteins Fip-lti1 and Fip-lti2 from Lentinus tigrinus in Concanavalin A-Induced Liver Oxidative Injury

机译:新型真菌免疫调节蛋白的保护功能FIP-LTI1和甘氨酸曲素苷诱导肝氧化损伤的肝脂素的FIP-LTI2

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Fungal immunomodulatory proteins (FIPs) are a class of small proteins that have been extensively studied for their immunomodulatory activities. In this study, two novel FIPs from Lentinus tigrinus were identified and named Fip-lti1 and Fip-lti2. The bioactive characteristics of Fip-lti1 and Fip-lti2 were compared to a well-known FIP (LZ-8 from Ganoderma lucidum) to investigate the effect of Fip-lti1 and Fip-lti2 expression on concanavalin A- (Con A-) induced liver oxidative injury. Both Fip-lti1 and Fip-lti2 protected the livers from Con A-induced necrosis, as evidenced by decreased serum aminotransferase levels (AST, ALT) and relieved liver histology. Levels of proinflammatory cytokines (TNF-α, IL-1β, and IL-6) and oxidative stress (SOD, MDA) were shown to be reduced by expressing Fip-lti1 and Fip-lti2. In addition, the hepatoprotective effect of Fip-lti1, Fip-lti2, and LZ-8 correlated with ameliorating the imbalance of Th1/Th2 (IFN-γ/IL-4). The observed liver protection of Fip-lti1 and Fip-lti2 was mechanistically explored. Treatments with Fip-lti1 and Fip-lti2 regulated GATA3/T-bet expression, activated the decreased Nrf-2/HO-1 pathway, and countered the upregulated NLRP3/ASC/NF-κBp65 signaling in Con A-stimulated liver injury. Nrf2 activation was shown to be involved in the mechanisms underlying the protection of Fip-lti by RNA interference. In conclusion, we identified two new fungal proteins (Fip-lti1 and Fip-lti2) that can protect the liver from Con A-induced liver oxidative injury through the Nrf2/NF-κB/NLRP3/IL-1β pathway.
机译:真菌免疫调节蛋白(FIPS)是一类小型蛋白质,其已被广泛研究其免疫调节活动。在这项研究中,鉴定了来自Lentinus Tigrinus的两种新型FIPS并命名为FIP-LTI1和FIP-LTI2。将FIP-LTI1和FIP-LTI2的生物活性特性与众所周知的FIP(来自Ganoderma lucidum的LZ-8)进行比较,以研究FIP-LTI1和FIP-LTI2表达对诱导的康酰丙胺素A-(CON A-)的影响肝氧化损伤。 FIP-LTI1和FIP-LTI2都保护肝脏免受CON诱导的坏死,如下降的血清氨基转移酶水平(AST,ALT)和缓解肝脏组织学证明。通过表达FIP-LTI1和FIP-LTI2,显示了促炎细胞因子(TNF-α,IL-1β和IL-6)和氧化应激(SOD,MDA)的水平。此外,FIP-LTI1,FIP-LTI2和LZ-8的肝保护作用与改善Th1 / Th2(IFN-γ/ IL-4)的不平衡相关。机械探索了观察到的FIP-LTI1和FIP-LTI2的肝脏保护。用FIP-LTI1和FIP-LTI2调节的GATA3 / T-BET表达的治疗,激活降低的NRF-2 / HO-1途径,并反对CON刺激的肝损伤中的上调的NLRP3 / ASC / NF-κBP65信号传导。显示NRF2激活参与通过RNA干扰保护FIP-LTI的机制。总之,我们鉴定了两种新的真菌蛋白(FIP-LTI1和FIP-LTI2),其可以通过NRF2 / NF-κB/ NLRP3 / IL-1β途径保护肝脏免受CON A诱导的肝脏氧化损伤。

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