Notch1 promotes renal tubulointerstitial fibrosis in renal tissues of diabetic mice by inhibiting autophagy through Akt/mTOR signaling pathway

AIM: To observe the changes of Notch1 expression and autophagy in the renal tissues of diabetic mice, and to explore the regulatory effect of Notch1 on tubulointerstitial fibrosis by inhibiting autophagy in diabetic nephro-pathy. METHODS: The mice were randomly divided into normal control group (db/m mice) and diabetes group (db/db mice), with 8 rats in each group. After 12 weeks of feeding, the mice were sacrificed and the corresponding biochemical indexes were measured. The protein expression of Notch1 in the renal tubular epithelial cells was observed by immunohistochemical staining. The protein levels of Notch1, PTEN, p-Akt (Thr308), Akt, p-mTOR (Ser2448), mTOR, LC3, P62, collagen type Ⅰ (Col-Ⅰ) and collagen type Ⅲ (Col-Ⅲ) were determined by Western blot. RESULTS: Compared with the db/m mice, the blood glucose, glycosylated hemoglobin, serum creatinine, triglyceride and total cholesterol were increased in the db/db mice (P<0.01). Renal tubular epithelial cell vacuolar degeneration, renal tubular expansion and interstitial inflammatory cell infiltration in db/db mouse renal tissues with HE staining were observed. The images of Masson staining showed collagenous fiber-like substance deposition in the glomerular capillaries and renal interstitium, and disarrangement of tubular structure in the renal tissues of db/db mice. The protein expression levels of PTEN and LC3-Ⅱ were decreased (P<0.01 or P<0.05), while the protein levels of Notch1, P62, p-mTOR (Ser2448), p-Akt (Thr308), Col-I and Col-III were increased in the db/db mice as compared with the db/m mice (P<0.01). However, no significant change of total mTOR and Akt proteins between the 2 groups was found. CONCLUSION: Notch1 protein expression was increased, PTEN expression was significantly reduced, Akt/mTOR pathway was activated, autophagy was inhibited, and fibrosis was aggravated in the renal tissues of the diabetic mice.     

气吸式覆膜精量油菜播种机排种性能试验与优化设计

针对目前高寒地油菜播种机普遍存在的重播漏播率高、人工劳动强度大、生长期缺水等问题，研究设计了一种气吸式精量播种机，一次性完成膜上播种、施肥、滴水灌溉、覆膜。分析了播种机主要结构、工作原理，对其关键部件进行结构设计，以排种盘转速、气吸室负压、排种盘型孔直径为试验因素，利用软件优化分析获得合理参数组合。结果表明：播种机排种盘转速197 r·min^-1、气吸室负压2.5 kPa、排种盘型孔直径1.2 mm时，田间播种合格率为93%、重播率3%、漏播率1%，播种质量较好。田间试验表明上述参数组合下排种器工作性能满足油菜播种机工作性能要求，该研究为油菜精密播种机的研究和设计提供了理论和技术参数。     

黑龙江省农产品深加工产业发展现状与对策

黑龙江省的农产品加工体系已经初步形成，但农业发展主要依赖于“原”字号产品。阐述了黑龙省农产品深加工产业建设存在的问题，通过分析制约农产品深加工产业发展的主要原因，从优化种植结构、整合现有资源、拓宽农产品销路以及提高农产品附加值4个方面提出解决对策。旨在做强食品加工业，上调农产品利润空间，通过“大龙头、大链条、大产业、大品牌的高效农业全产业链”促进粗放农产品向高附加值产品的转变，努力实现从产粮大省到农业强省的新跨越。      

植物免疫诱导剂在草莓中的应用情况

为了助力实现草莓的安全生产,对一类能诱导植物产生免疫防御反应的植物免疫诱导剂在草莓中的应用情况进行综述。主要阐述了植物免疫诱导剂的种类、诱导机理及其在草莓栽培上的应用现状,发现:植物免疫诱导剂能促进草莓生长和发育、诱导抗病性、提高产量、改善果实品质、提高耐贮性等,从而减少了化学农药的使用,有利于草莓高质量生产,应用前景广阔。     

南海大顶苦瓜规范化栽培技术

为了发挥广东省佛山市的传统特色蔬菜——大顶苦瓜的产品优势,提高农户的规范化栽培技术水平,在改良南海大顶苦瓜品种的基础上,制定出配套的规范化栽培技术措施,内容包括品种特性、产地环境要求、育苗、田间管理措施和采收,旨在进一步提高南海大顶苦瓜的生产效益,大力推广这一传统特色蔬菜品种。     

利用酵母双杂交系统筛选与草莓镶脉病毒移动蛋白P1互作的寄主因子

 构建感染草莓镶脉病毒(SVBV)森林草莓的酵母cDNA文库,利用酵母双杂交系统,筛选出与SVBV P1蛋白互作的15种寄主因子。生物信息学分析发现,这15种寄主因子参与茉莉酸途径、泛素化、光合作用、抗病抗逆、蛋白修饰、蛋白运输和氧化还原等多种生物过程。另外,这些寄主因子还具有其他分子功能,包括氧化还原酶活性、蛋白二硫化物异构酶活性和金属离子结合活性等。本研究初步探讨了P1与寄主因子的互作机理,为揭示SVBV侵染森林草莓以及SVBV在寄主中扩展的分子机制提供理论依据。     

灌溉方式与基施磷素对设施黄瓜产量的影响

以黄瓜为试材,采用小区试验对比的方法,研究了滴灌和畦灌条件下不同磷素用量对秋季大棚黄瓜产量的影响,以期为提高秋季大棚黄瓜产量提供参考依据。结果表明:滴灌大棚的黄瓜生长状况明显好于畦灌大棚,商品黄瓜产量显著提高(P0.05),各阶段用水总量278.3 mm,节水达41%。畦灌条件下,不施磷肥处理黄瓜果实产量显著低于磷肥处理(P0.05);滴灌条件下,过量的磷肥施用(P2O5100 kg·hm~(-2))导致黄瓜果实产量和品质显著下降(P0.05)。由此可见,滴灌条件下合理施用磷肥能够降低水资源消耗,提高磷肥利用效率,有利于黄瓜品质和产量的提升。     

miR-204 inhibits proliferation of Hodgkin lymphoma cells by targeting Sirt1/p53 signaling pathway

AIM: To investigate the effect of microRNA-204 (miR-204) on the proliferation of Hodgkin lymphoma cells and the underlying mechanism. METHODS: The expression of miR-204 and Sirt1 mRNA in Hodgkin lymphoma tissues was detected by RT-qPCR. After transfection with miR-204 mimic, Sirt1 siRNA and miR-204 mimic+pcDNA3.1-Sirt1 into the L428 cells, the cell viability and BrdU incorporation were measured by CCK-8 assay and BrdU assay, respectively. The protein levels of Sirt1 and acetylated p53 (ac-p53) were determined by Western blot.The targeting relationship between miR-204 and Sirt1 was verified by double luciferase reporter assay. RESULTS: The low expression of miR-204 and the high mRNA expression of Sirt1 were found in the Hodgkin lymphoma tissues. Compared with control group, the cell viability, BrdU incorporation and the protein levels of Sirt1 and ac-p53 were significantly decreased after L428 cells were transfected with miR-204 mimic or Sirt1 siRNA (P<0.05). Compared with miR-204 mimic alone group, the cell viability, BrdU incorporation and the protein levels of Sirt1 and ac-p53 were increased after L428 cells were co-transfected with miR-204 mimic and pcDNA3.1-Sirt1 (P<0.05). The results of double luciferase reporter assay confiermed that Sirt1 was the target gene of miR-204. CONCLUSION: The inhibitory effect of miR-204 on the proliferation of L428 cells may be achieved by inhibiting the expression of Sirt1 and promoting the up-regulation of ac-p53.     

香蕉与B基因组相关的SCAR标记研究

香蕉(Musa L.)是由2个二倍体野生种Musa acuminata Colla(AA基因型)和Musa balbisiana Colla(BB基因型)种内或种间杂交进化而来,其B基因组中带有重要的优良基因。利用与香蕉B基因组相关的gypsy-IRAP分子标记,成功开发了一对SCAR引物,适用于鉴定尖叶蕉(AAw)、长梗蕉(BB)、香牙蕉(AAA)、贡蕉(AAcv)、大蕉、粉蕉(ABB)、粉大蕉(ABB)、龙牙蕉(AAB)以及四倍体香蕉(AAAB)等是否含有B基因组。     

Effect of proline-spirooxindole on viability and apoptosis of non-small-cell lung cancer A549 cells

AIM:To investigate the effect of proline-spirooxindole on the viability and apoptosis of human non-small-cell lung cancer A549 cells. METHODS:The effect of proline-spirooxindole on the viability of A549 cells was determined by CCK-8 assay. The apoptosis was analyzed by flow cytometry. The effects of proline-spirooxindole on the expression of PARP and p53 and the phosphorylation of mTOR were determined by Western blot. RESULTS:After A549 cells were treated with proline-spirooxindole (25, 50 and 100 mg/L), the cell viability was decreased (P<0.01) compared with DMSO control group. The apoptotic rate was increased compared with DMSO control group (P<0.01). The protein expression of p53 was up-regulated, the increased apoptotic protein cleaved PARP was observed, and the phosphorylation of mTOR was inhibited (P<0.01). CONCLUSION:Proline-spirooxindole inhibits the viability of A549 cells and induces apoptosis, which may be related to the phosphorylation of mTOR.