Regulation of MMP-2 and TIMP-3 expression by uPA signal transduction system in human bone giant cell tumor

AIM: To study effects of urokinase-type plasminogen activator (uPA) signal transduction on expression of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of matrix metalloproteinase-3 (TIMP-3) in giant cell tumor of bone (GCT). METHODS: Expression of uPAR, MMP-2 and TIMP-3 in GCT tissue was detected by immunohistochemistry. Phosphorylation level of mitogen-activated protein kinase (p44) in uPA/uPAR signal pathway in cultured GCT cells was detected by immunoprecipitation. The expression of MMP-2 and TIMP-3 in cultured cells after treatment with uPA-ATF or anti-uPAR antibody was also detected by Western blotting. RESULTS: 1) Urokinase-type plasminogen activator receptor (uPAR) was positive on the cell membrane and in cytoplasm of some mononuclear stromal cells (MSCs) and multinucleated giant cells (MGCs); 2) MMP-2 was positive in the cytoplasm and on the cell membrane of almost all of MSCs and some of MGCs. The polar distribution of MMP-2 in the cytoplasm of MGCs was especially obvious; 3) The expression of TIMP-3 of some MSCs and MGCs in GCT was much lower than MMP-2. The positive signal also showed a prominent polarity; 4) After treatment with uPA-ATF, the phosphorylation level of p44 in GCT cultured cells was much higher than the control. Addition of anti-uPAR antibody in the cells remarkably down-regulated the phosphorylation level of p44 as compared with the control group, suggesting that uPA-ATF participates cell signal transduction and this reaction can be inhibited by anti-uPAR antibody; 5) uPA-ATF cell signal pathway up-regulated expression of MMP-2 and TIMP-3, while anti-uPAR antibody down-regulated the expression of MMP-2 and TIMP-3. CONCLUSION: These results demonstrate for the first time that uPA-ATF directly regulates the expression of MMP-2 and TIMP-3 by signal transduction pathway, and the over-expression of MMP-2 and TIMP-3 may play an important role in local osteolysis of GCT.     

中国美利奴多胎细毛羊及杂交后代多胎性状基因型分析

首次在国内采用了多胎性状基因型诊断法对多胎性状进行选择。试验采集中国美利奴多胎细毛羊及其与Romilly·Hills杂交后代、横交一代样品数分别为 47份、3 8份、2 6份 ,提取DNA确定多胎主效基因FecB 位点 ,酶切检测纯合基因BB、杂合基因B 和非多胎基因 。通过检测 ,三种基因型占样品数百分比分别为 :多胎细毛羊为 2 5 5 3 %、48 94%、2 5 5 3 % ,基因型与产羔符合率为 85 3 7% ;杂交一代为 0、76 3 2 %、2 3 68% ,基因型与产羔符合率为 76 19% ;横交一代为3 0 77%、5 7 69%、11 5 4%。在多胎性状的选择中 ,要坚决剔除非多胎基因个体 ,以缩短选育时间。     

几种绿色饲料添加剂在肉鸡生产上的应用效果

选1日龄AA肉鸡390只,分成13组,分别添加不同种类和不同种类组合的绿色饲料添加剂。试验结果表明,益生素能显著(p<0.05)提高肉鸡的生产性能,改善肉品质。     

日粮维生素E水平对后备种母鸡生长发育的影响

研究日粮维生素E对后备种母鸡体形、肌肉和生殖器官生长发育的影响。发现日粮维生素E水平对20周龄后备种母鸡的体重、体重均匀度、胸骨长度、胫长度、屠宰率、半净膛率、全净膛率、胸肌率、腿肌率、翅重率、腹脂率、冠高度和卵巢重量没有显著影响(P>0 05 ), 但高剂量维生素E日粮显著增加输卵管的长度和重量(P<0 05)。结果表明日粮高维生素E水平(180mg/kg) 可加速20周龄后备种母鸡输卵管的生长发育。     

母牛一胎双犊技术的研究

选择9头母牛先行人工授精、7天后再移植冷冻胚胎以生产双犊。试验结果表明,母牛产双犊达44.44%(P<0.01)。提示:采用A(I人工授精)+ET(胚胎移植)是提高母牛双犊率的有效技术措施之一。     

混合比例和添加剂对菊苣与青贮玉米混合青贮品质的影响

探讨不同混合比例和添加剂对菊苣和青贮玉米混合青贮饲料品质的影响,为调制高质量的混合青贮饲料提供理论依据。以菊苣和青贮玉米为原料,按质量比0∶1、1∶3、1∶1、3∶1和1∶0 (分别用0C1M、1C3M、1C1M、3C1M、1C0M表示)进行混合青贮,并分别设置3个添加剂处理,即零添加、5 g·t^-1乳酸菌+5 g·t^-1纤维素酶(LX)和10 g·t^-1乳酸菌+5 g·t^-1纤维素酶(2LX),青贮60 d后测定混合青贮饲料的营养成分和发酵品质。结果显示,菊苣与青贮玉米混合比例为0∶1和1∶1时青贮饲料的感官评价优于其余3种混合比例的,而且添加剂处理感官评定优于零添加处理的。菊苣和青贮玉米混合青贮可以形成养分互补,有助于均衡青贮饲料整体营养,在青贮原料中添加添加剂则可以提高青贮饲料发酵品质。混合青贮饲料的营养价值随菊苣比例增加而显著提高,但是发酵品质在菊苣混合青贮比例高于1∶1时显著降低。综合判定菊苣和青贮玉米1∶1混合时其青贮饲料品质最佳,其中又以1C1M/2LX处理最好,纤维组分(NDF和ADF)和氨态氮/总氮含量较低而粗蛋白和乳酸含量较高。     

高寒区轮作模式对当归田土壤特性及药材产量的影响

连作重茬造成当归产量逐年下降。采用药用植物秦艽(QJ)、羌活(QH)轮作当归(DG),以当归连作为对照,通过测定土壤和药材产量指标,利用主成分分析确定各指标权重,并结合隶属综合因子分析和聚类分析,旨在揭示不同药用作物轮作当归对土壤环境与药材产量的影响,为筛选适宜当归栽培的轮作模式提供科学依据。结果表明,不同作物轮作对当归田土壤特性和药材产量均具有显著影响,秦艽轮作当归可有效改善土壤特性,使当归成药期土壤磷和钾含量处于较低水平,而有机质维持在较高水平,对土壤水分的季节调控作用更为显著,与当归连作相比较,当归成药率提高94.10%,药材单根鲜重和药材鲜产量分别提高53.46%和125.56%,而羌活轮作当归土壤pH最高,有机质含量最低,当归连作土壤有机质含量虽高,但土壤富集磷和钾,对土壤水分季节性调控作用最小,当归成药率和药材产量均低。不同轮作模式当归成药率和药材产量依次为秦艽-当归>当归-当归>羌活-当归,综合指数大小依次为秦艽-当归(0.8132)>羌活-当归(0.3315)>当归连作(0.2051)。聚类分析将3种轮作模式分为三大类,重复小区亚类间距离均小,说明不同作物轮作对土壤的调控作用不同,高寒产区秦艽轮作当归是优化调控土壤环境,提高当归产出性能的有效轮作模式。     

The IMPDH inhibitors,ribavirin and mycophenolic acid,inhibit peste des petits ruminants virus infection

Peste des petits ruminants virus (PPRV) causes highly contagious diseases in domestic and particular wild small ruminants, leading to substantial economic loss. The development of effective and cheap antiviral medications shall help to circumvent this emerging burden. In this study, we found that ribavirin, a competitive inosine-5’-monophosphate dehydrogenase (IMPDH) inhibitor, significantly inhibits the replication of PPRV. As IMPDH is a key enzyme in purine nucleotide synthesis, supplementation of exogenous guanosine attenuate the anti-PPRV effect of ribavirin. Interestingly, an uncompetitive IMPDH inhibitor, mycophenolic acid (MPA), exerted more potent antiviral effect again PPRV. Similarly, this effect was largely restored upon supplementation of guanosine. Thus, we have demonstrated that the IMPDH inhibitors ribavirin and MPA combat PPRV infection through purine nucleotide depletion. Because both regimens have been widely used in the clinic for treating viral infection or organ rejection in transplantation patients for decades, respectively, repurposing these existing safe and cheap medications may provide a new avenue for combating PPRV infection.     

Branched‐chain amino acid ratios in low‐protein diets regulate the free amino acid profile and the expression of hepatic fatty acid metabolism‐related genes in growing pigs

Liver metabolism is affected by nutrients. The aim of this study was to explore the effects of low‐protein diets (17% crude protein, CP) supplemented with branched‐chain amino acids (BCAAs), including leucine (Leu), isoleucine (Ile) and valine (Val), on hepatic amino acid profile and lipid metabolism in growing pigs. The ratio of Leu : Ile : Val in all groups was 1 : 0.51 : 0.63 (20% crude protein, CP), 1 : 1 : 1 (17% CP), 1 : 0.75 : 0.75 (17% CP), 1 : 0.51 : 0.63 (17% CP) and 1 : 0.25 : 0.25 (17% CP) respectively. Results revealed that compared to the positive control group (1 : 0.51 : 0.63, 20% CP), the low‐protein diets significantly augmented the concentrations of most essential amino acids and non‐essential amino acids (p < .05), with the greatest values observed in the 1 : 0.25 : 0.25 group. Moreover, relative to the control, the low‐protein diets with the Leu : Ile : Val ratio ranging from 1 : 0.75 : 0.75 to 1 : 0.25 : 0.25 markedly downregulated the mRNA abundance of acetyl‐CoA carboxylase (ACC), lipoprotein lipase (LPL) and fatty acid‐binding protein 4 (FABP‐4) (p < .05), and upregulated the mRNA expression of hormone‐sensitive lipase (HSL), peroxisome proliferator‐activated receptor‐g coactivator‐1α (PGC‐1α), uncoupling protein 3 (UCP3) and liver carnitine palmitoyltransferase 1 (L‐CPT‐1) (p < .05). Therefore, our data suggest that protein‐restricted diets supplemented with optimal BCAA ratio, that is, 1 : 0.75 : 0.75–1 : 0.25 : 0.25, induce a shift from fatty acid synthesis to fatty acid oxidation in the liver of growing pigs. These effects may be associated with increased mitochondrial biogenesis.