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1.
实验以大菱鲆(Scophthalmus maximus)幼鱼[(14.00±0.02)g]为研究对象,采用2×4双因素设计,设2个VE水平(0和75 mg/kg)和4个L-肌肽水平(0、50、100和200 mg/kg),研究VE和L-肌肽对其生长、抗氧化、非特异性免疫及血清生化指标的影响。实验共分8组,每组3个重复,每个重复46尾鱼,实验周期为8周。结果显示:(1)在饲料中添加75 mg/kg VE显著提高了大菱鲆幼鱼增重率(WGR)和特定生长率(SGR)(P < 0.05),L-肌肽添加量≤100 mg/kg对实验鱼生长性能无显著影响(P>0.05),添加量为200 mg/kg时鱼体WGR、SGR和蛋白质效率(PER)显著降低,饲料系数(FCR)显著升高(P < 0.05);(2)VE和L-肌肽对血清谷胱甘肽过氧化物酶(GSH-PX)、过氧化氢酶(CAT)活性和丙二醛(MDA)含量及肝脏总抗氧化能力(T-AOC)、超氧化物歧化酶(SOD)活性和MDA含量均具有显著的交互作用(P < 0.05),在VE 75 mg/kg水平下,L-肌肽添加量为50和100 mg/kg时血清GSH-PX活性最高,L-肌肽添加量为100和200 mg/kg时血清CAT活性最高且与添加量为50 mg/kg差异不显著(P>0.05),添加100 mg/kg肝脏T-AOC和SOD活性达到最高且50 mg/kg组的SOD与100 mg/kg组差异不显著(P>0.05),主效应结果显示,VE显著提高了血清T-AOC、SOD及肝脏CAT活性(P < 0.05),L-肌肽显著提高了血清T-AOC(P < 0.05);(3)VE和L-肌肽对血清补体C3和LZM活性交互作用显著,在75 mg/kg VE水平下,L-肌肽添加量为50 mg/kg时,补体C3水平最高(P < 0.05),主效应显示,VE和L-肌肽对血清总蛋白(TP)影响均不显著(P>0.05);(4)添加VE显著降低了血清总胆固醇(TCHO)和甘油三酯(TG)含量(P < 0.05),添加L-肌肽显著降低了血清TG含量,且在L-肌肽50 mg/kg时达到最低。综合考虑大菱鲆幼鱼[(14.00-39.43)g]的生长性能、抗氧化性能、非特异性免疫及血清生化指标得出,在实验配方条件下(鱼油70 g/kg,大豆卵磷脂10 g/kg),添加VE 75 mg/kg时,L-肌肽的适宜添加量为50 mg/kg。  相似文献   
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SPHK1 (sphingosine kinase 1), a regulator of sphingolipid metabolites, plays a causal role in the development of hepatocellular carcinoma (HCC) through augmenting HCC invasion and metastasis. However, the mechanism by which SPHK1 signaling promotes invasion and metastasis in HCC remains to be clarified. Here, we reported that SPHK1 induced the epithelial-mesenchymal transition (EMT) by accelerating CDH1/E-cadherin lysosomal degradation and facilitating the invasion and metastasis of HepG2 cells. Initially, we found that SPHK1 promoted cell migration and invasion and induced the EMT process through decreasing the expression of CDH1, which is an epithelial marker. Furthermore, SPHK1 accelerated the lysosomal degradation of CDH1 to induce EMT, which depended on TRAF2 (TNF receptor associated factor 2)-mediated macroautophagy/autophagy activation. In addition, the inhibition of autophagy recovered CDH1 expression and reduced cell migration and invasion through delaying the degradation of CDH1 in SPHK1-overexpressing cells. Moreover, the overexpression of SPHK1 produced intracellular sphingosine-1-phosphate (S1P). In response to S1P stimulation, TRAF2 bound to BECN1/Beclin 1 and catalyzed the lysine 63-linked ubiquitination of BECN1 for triggering autophagy. The deletion of the RING domain of TRAF2 inhibited autophagy and the interaction of BECN1 and TRAF2. Our findings define a novel mechanism responsible for the regulation of the EMT via SPHK1-TRAF2-BECN1-CDH1 signal cascades in HCC cells. Our work indicates that the blockage of SPHK1 activity to attenuate autophagy may be a promising strategy for the prevention and treatment of HCC.  相似文献   
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Based on central dogma of genetics, protein is the embodiment and executor of genetic function, post-translational modifications (PTMs) of protein are particularly important and involved in almost all aspects of cell biology and pathogenesis. Studies have shown that ionizing radiation (IR) alters gene expression much more profoundly and a broad variety of cell-process pathways, lots of proteins are modified and activated. Our understanding of the protein in response to ionizing radiation is steadily increasing. Among the various biological processes known to induce radioresistance, PTMs have attracted marked attention in recent years. The present review summarizes the latest knowledge about how PTMs response to ionizing radiation and pathway analysis were conducted. The data provided insights into biological effects of IR and contributing to the development of novel IR-based strategies.  相似文献   
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High-molecular-weight glutenin subunits (HMW-GS) in wheat grain are the major determinants of dough elasticity and viscosity and thus of bread-making quality. PCR-based molecular markers designed based on DNA polymorphisms were used to analyze HMW-GS genes in wheat. The loop-mediated isothermal amplification (LAMP) assay is a simple and rapid method for specific detection of genomic DNA target sequences. In the present study, we designed a set of LAMP markers by targeting the unique sequences of 1Dx2 and 1Dx5 genes. The primers could effectively distinguish the 1Dx2 and 1Dx5 genes from other genes at the Glu-1 locus. The results were confirmed by agarose gel electrophoresis. For visualization, ethidium bromide was used, and fluorescence only appeared in the positive samples. Under optimal conditions, the detection could be finished in 1 h. Thirty-eight wheat cultivars with known HMW-GS were used to validate LAMP markers for 1Dx2 and 1Dx5 genes. Only DNA samples with target genes could be amplified, and the results could be read easily using this method. The tests using LAMP were easy to perform, rapid, and sensitive. Thus, the current study results have the potential to be a powerful tool for the detection of HMW-GS genes in wheat.  相似文献   
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Here an all‐purpose fibrous electrode based on MoS2 is demonstrated, which can be employed for versatile energy harvesting and storage applications. In this coaxial electrode, ultrathin MoS2 nanofilms are grown on TiO2 nanoparticles coated carbon fiber. The high electrochemical activity of MoS2 and good conductivity of carbon fiber synergistically lead to the remarkable performances of this novel composite electrode in fibrous dye‐sensitized solar cells (showing a record‐breaking conversion efficiency of 9.5%) and high‐capacity fibrous supercapacitors. Furthermore, a self‐powering energy fiber is fabricated by combining a fibrous dye‐sensitized solar cell and a fibrous supercapacitor into a single device, showing very fast charging capability (charging in 7 s under AM1.5G solar illumination) and an overall photochemical‐electricity energy conversion efficiency as high as 1.8%. In addition, this wire‐shaped electrode can also be used for fibrous Li‐ion batteries and electrocatalytic hydrogen evolution reactions. These applications indicate that the MoS2‐based all‐purpose fibrous electrode has great potential for the construction of high‐performance flexible and wearable energy devices.  相似文献   
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