长期施肥对黄土旱塬农田土壤微生物量碳、氮、磷的影响

为研究长期不同施肥方式对土壤微生物量碳、氮、磷含量的影响,以国家黄土高原农业生态试验站长期定位施肥试验为研究对象,选取不施肥(CK)、单施氮肥(N)、单施磷肥(P)、施氮磷肥(NP)、单施有机肥(M)、氮肥配施有机肥(NM)、磷肥配施有机肥(PM)、氮磷肥配施有机肥(NPM)8个处理,应用氯仿熏蒸-浸提法和生态化学计量比,研究了30 a不同施肥方式下土壤微生物量碳、氮、磷含量变化及其与土壤基本理化性状的关系。结果表明:长期施肥较CK处理均能提高土壤微生物量氮、磷含量;与CK相比,施用化肥处理的微生物量碳含量均有所降低,而微生物量氮、磷含量显著提高;除NM处理外,施用有机肥处理的土壤微生物量碳、氮、磷含量较CK处理均显著提高。长期单施化肥、有机肥和化肥有机肥配施处理的微生物量C∶N显著低于CK处理,等量施磷处理(P、NP、PM、NPM)的微生物量C∶P、N∶P均低于CK和其余施肥处理,而NM处理的微生物量C∶P、N∶P显著高于其余处理。冗余分析显示,土壤全氮(F=13.9,P=0.002)对土壤微生物生物量影响最大,解释了微生物量变化的5.3%,各理化性质的影响顺序为全氮全磷pH有机质;相关性分析表明,土壤微生物量碳、磷分别与土壤有机质、全氮、全磷呈显著正相关,土壤微生物量氮与有机质、全氮呈显著正相关。长期单施化肥使土壤酸碱度发生改变,对微生物的生命活动产生抑制作用。而长期化肥配施有机肥能不同程度提高土壤养分含量,促进土壤微生物的生长繁殖,进而增强微生物对碳、氮、磷等元素的吸收利用,对于提高土壤肥力和肥料利用率具有重要意义。     

Advances on studies of miR-21 in vascular endothelial function and angiogenesis

MicroRNAs (miRNAs)are a class of non-coding, endogenous, single-stranded small RNA molecules composed of 19~25 nucleotides. miRNAs are widely involved in the process of human life activities. Recent studies have shown that part of miRNAs regulate the vascular endothelial function and angiogenesis. High expression of miRNA-21 is found to play important roles in the cell proliferation, cell apoptosis, cell growth and death of vascular endothelial cells. This review will focus on the recent progress related to miRNAs in vascular endothelial function and angiogenesis, providing a new insight in cardiovascular disease prevention, clinical diagnosis, prognosis and target therapeutics.     

放牧压力对草原砂质栗钙土微生物量C,N,P影响的研究

对不同放牧压力下草原砂质栗钙土微生物量C、N、P进行较为系统地研究。结果表明：就土壤原土来看,随着放牧压力的增大,土壤微生物量C,N先增加后减少;土壤微生物量C在放牧率2.67只羊/hm2时相对较高,微生物量P随着放牧压力的增大逐渐降低。     

Effect of xeroderma pigmentosum group D gene on proliferation of human umbilical arterial smooth muscle cells induced by Ox-LDL

AIM: To investigate the effects of xeroderma pigmentosum group D (XPD) gene on the proliferation of human umbilical arterial smooth muscle cells (HUASMCs) induced by oxidized low-density lipoprotein (Ox-LDL). METHODS: The recombinant plasmid pEGFP-N2/XPD was transfected into HUASMCs by liposome. The cells were divided into blank control group, pEGFP-N2 group, pEGFP-N2/XPD group, Ox-LDL group, Ox-LDL+pEGFP-N2 group and Ox-LDL+pEGFP-N2/XPD group. The proliferation rate of the cells was detected by MTT and EdU assays. The apoptotic rate and cell cycle distribution were analyzed by flow cytometry. The protein levels of XPD, caspase-3, Bcl-2 and Bax were determined by Western blot. RESULTS: Compared with blank control group, the expression of XPD was increased in pEGFP-N2/XPD group (P<0.05). According to the results of MTT and EdU assays, the cell proliferation in pEGFP-N2/XPD group was reduced compared with blank control group (P<0.05). Compared with Ox-LDL group, the cell proliferation in Ox-LDL+pEGFP-N2/XPD group was significantly inhibited (P<0.05). According to the results of flow cytometry, the cell proportion of S phase decreased and the G₀/G₁-phase cell proportion increased significantly in pEGFP-N2/XPD group and Ox-LDL+pEGFP-N2/XPD group compared with blank control group and Ox-LDL group, repectively (P<0.05). Compared with blank control group and Ox-LDL group, the protein level of Bcl-2 decreased and the protein levels of Bax and cleaved caspase-3 increased in pEGFP-N2/XPD group and Ox-LDL+pEGFP-N2/XPD group, respectively (P<0.05). CONCLUSION: XPD inhibits the proliferation of HUASMCs and promotes their apoptosis, and reduces the promoting effect of Ox-LDL on the proliferation of HUVSMCs. XPD may be the target for treatment of atherosclerosis.     

解淀粉芽孢杆菌GB58对水稻纹枯病的防效及菌剂载体筛选

旨在对解淀粉芽孢杆菌GB58在水稻纹枯病上的盆栽防治效果和最佳菌剂载体进行研究，明确其应用前景。采用盆栽试验测定GB58对水稻纹枯病的病斑高率和在水稻上的定殖能力，测定GB58在菌剂固定载体的吸附能力和吸附稳定性。盆栽试验结果表明，GB58在水稻病株上有良好的定殖效果，定殖数最大达到2.22×10⁷ cfu/g。与喷施井冈霉素处理相比，GB58对水稻纹枯病的防效在病害发生后20、40天分别显著提高了20%、24%。GB58在固体菌剂吸附载体的研究表明：结合菌体吸附量、存活率和抑菌活性进行分析，有机载体吸附效果好于无机载体；同时综合考虑应用价值，选择玉米粉、有机肥为菌剂吸附载体较好。GB58对水稻纹枯病具有较好的生防效果。采用玉米粉和有机肥作为固体菌剂吸附载体，具有经济、高效的特点，有较大的应用价值与开发潜力。     

激素对奶牛乳腺上皮细胞乳脂肪合成的调控作用

乳脂肪是高质量的天然脂肪，其可为人类提供营养和能量，在各种膳食脂肪和油类中，是最容易被消化吸收的。乳脂肪是在乳腺中由从头合成或外源摄取的脂肪酸与甘油酯化形成的一种脂类物质，其含量的高低关系着牛奶品质的优劣和乳制品的加工特性。在奶牛的泌乳周期中，乳腺泌乳功能受多种因素影响，其中内分泌腺分泌的多种激素对奶牛乳腺上皮细胞（BMECs）乳脂的合成具有积极的调控作用。综上所述，作者介绍了氢化可的松、催乳素、胰岛素和生长激素4种泌乳相关激素对BMECs乳脂肪合成的调控机理，即从乳脂合成适宜的激素添加量、激素对乳脂球形态的影响方面初步阐释其调控作用，并从乳脂合成的关键酶及转录因子、激素对乳脂合成相关基因表达量方面深入阐释其作用机理，旨在为研究泌乳相关激素对奶牛乳腺内乳脂肪合成的调控机理提供参考。     

Oxygen isotope ratios of plant available phosphate in lowland tropical forest soils

Phosphorus (P) cycles rapidly in lowland tropical forest soils, but the process have been proven difficult to quantify. Recently it was demonstrated that valuable data on soil P transformations can be derived from the natural abundance of stable oxygen isotopes in phosphate (δ¹⁸O_P). Here, we measured the δ¹⁸O_P of soils that had received long-term nutrient additions (P, nitrogen, and potassium) or litter manipulations in lowland tropical forest in Panama and performed controlled incubations of fresh soils amended with a single pulse of P. To detect whether δ¹⁸O_P values measured in the incubations apply also for soils in the field, we examined the δ¹⁸O_P values after rewetting dry soils. In the incubations, resin-P δ¹⁸O_P values converged to ∼3.5‰ above the expected isotopic equilibrium with soil water. This contrasts with extra-tropical soils in which the δ¹⁸O_P of resin-P matches the expected equilibrium with soil water. Identical above-equilibrium resin-P δ¹⁸O_P values were also found in field soils that did not receive P additions or extra litter. We suggest that the 3.5‰ above-equilibrium δ¹⁸O_P values reflect a steady state between microbial uptake of phosphate (which enriches the remaining phosphate with the heavier isotopologues) and the release of isotopically equilibrated cell internal phosphate back to the soil. We also found that soil nutrient status affected the microbial turnover rate because in soils that had received chronic P addition, the original δ¹⁸O_P signature of the fertilizer was preserved for at least eight weeks, indicating that the off-equilibrium δ¹⁸O_P values produced during microbial phosphate turnover was not imprinted in these soils. Overall, our results demonstrate that ongoing microbial turnover of phosphate mediates its biological availability in lowland tropical soils.     

Effect of CHOP expression knock-down on apoptosis of renal tubular epithelial cells

AIM:To study the effect of C/EBP homologous protein (CHOP) on the apoptosis of renal tubular epithelial HK2 cells. METHODS:The serum mRNA levels of CHOP in the patients with acute kidney injury and healthy controls were detected by qPCR. In vitro, renal tubular epithelial HK2 cells were divided into control group, negative group (transfected with negative control siRNA), si-CHOP group (transfected with CHOP siRNA), and induced by transforming growth factor-β1 (TGF-β1). The viability of the cells was measured by MTT assay, and the apoptotic rate was analyzed by flow cytometry. The protein levels of nuclear antigen Ki-67, proliferating cell nuclear antigen (PCNA), caspase-3 and cleaved caspase-3 were determined by Western blot. RESULTS:Compared with the healthy controls, the serum mRNA levels of CHOP in the patients with acute kidney injury were increased significantly (P<0.05). Transfection with CHOP siRNA significantly decreased the expression of CHOP in the renal tubular epithelial HK2 cells (P<0.05). Knock-down of CHOP expression by siRNA significantly increased the viability of renal tubular epithelial HK2 cells (P<0.05), decreased the apoptotic rate (P<0.05), increased the expression of Ki-67 and PCNA (P<0.05), and down-regulated the protein level of cleaved caspase-3 (P<0.05). CONCLUSION:The serum mRNA levels of CHOP were increased in the patients with acute kidney injury. Knock-down of CHOP expression inhibits the apoptosis of renal tubular epithelial cells by regulating the expression of proliferation-and apoptosis-related proteins.     

Role of miR-219 and TGFBR2 in pathogenesis of renal fibrosis

AIM:To study the role of microRNA-219 (miR-219) in regulation of transforming growth factor-β receptor type 2 (TGFBR2) in renal fibrosis. METHODS:The renal fibrosis patients (n=70) were selected in this stu-dy, and 20 cases of healthy people were selected as control group. RT-qPCR was used to detect the expression of miR-219 in the serum of the patients with renal fibrosis and control group, and the expression of miR-219 in NRK49F cells after stimulation with angiotensin Ⅱ(AngⅡ) was detected. The protein expression of α-smooth muscle actin (α-SMA) in the NRK49F cells transfected with miR-219 mimics after stimulation with AngⅡ was determined by Western blot. The potential target gene TGFBR2 of miR-219 was screened and verified by the method of luciferase reporter gene. RT-qPCR and Western blot were used to detected the effect of miR-219 mimics on the expression of TGFBR2 at mRNA and protein levels, and the mRNA expression of α-SMA, connective tissue growth factor (CTGF), type I collagen α1 (COL1A1) and COL3A1 in the NRK49F cells was also detected, respectively. The unilateral ureteral occlusion (UUO) mouse model was established and the expression of miR-219 in the renal tissue was monitored. The morphological change of renal fibrosis was observed in the UUO mice after injection of miR-219, and the mRNA expression levels of COL1A1 and COL3A1 were detected. RESULTS:The expression level of miR-219 in the patients with renal fibrosis was significantly lower than that in control group, and the expression of miR-219 in the UUO mice was decreased significantly (P<0.01). The expression level of miR-219 was significantly decreased in the NRK49F cells after AngⅡ stimulation, and miR-219 mimics inhibited the protein expression of α-SMA(P<0.01). miR-219 mimics had a targeted regulatory effect on TGFBR2 gene, which inhibited the mRNA and protein expression of TGFBR2. miR-219 mimics inhibited the mRNA expression of α-SMA, CTGF, COL1A1 and COL3A1. miR-219 also down-regulated the mRNA expression of COL1A1 and COL3A1 in the UUO mice and inhibited the process of renal fibrosis. CONCLUSION:miR-219 inhibits the development of renal fibrosis by inhibiting the expression of TGFBR2, which may become a new target for the diagnosis and treatment of renal fibrosis.