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.     

Acupuncture and traditional Chinese veterinary medicine for treatment of a mare with rectal paralysis

An 8‐year‐old Appaloosa mare with rectal paralysis due to a cosmetic ethanol ‘tail block’ was treated with traditional Chinese veterinary medicine treatments including acupuncture and herbal medicine. Her rectal and tail tone gradually improved after the treatment. At 4 months after initial presentation, the mare was able to produce faecal piles on a regular basis, and manual evacuations were no longer needed. Significant improvement was within 30 days of beginning treatment. At 8 months, the owner indicated that the mare had normal defaecation, was able to swish the tail from side to side and lift the tail to urinate, and had no evidence of straining to defaecate or colic.     

低温胁迫对细茎柱花草与TPRC2001-1柱花草抗寒生理指标的影响

为了探究柱花草的抗寒性,本研究以细茎柱花草(Stylosanthes guianensis var.intermedia)和TPRC2001-1柱花草(S.guianensis‘TPRC2001-1’)营养期叶片为材料,分别进行时长为0(对照)、24h和48h的低温处理,然后对其相对电导率、丙二醛、脯氨酸、可溶性糖以及可溶性蛋白的含量等指标进行测定与分析。结果表明,两种柱花草叶片的抗寒性生理指标随着低温处理时间的增加逐步上升。低温处理后,细茎柱花草的相对电导率和丙二醛含量显著低于TPRC2001-1柱花草(P0.05),而脯氨酸、可溶性糖和可溶性蛋白的含量显著高于TPRC2001-1柱花草(P0.05)。综合各项生理指标可得,两种柱花草的抗寒性强弱为细茎柱花草TPRC2001-1柱花草。     

试论我国“注水肉”监管技术体系建设

"注水肉"监管存在判定标准单一的问题,亟须建立畜禽肉监管技术体系。本文借鉴发达国家"消费理念引导"和"市场行为约束"理念,提出以"正常为主"为判定原则,从畜禽宰前管理、屠宰及市场监管多环节入手,通过畜禽行为学、组织形态学、正常肉敏感指标范围、近红外等特征图谱,以及畜禽肉水分限量等指标,提出了构建"注水肉"监管技术体系的新思路。     

2018年山东省诸城市小反刍兽疫免疫效果横断面调查

为掌握山东省诸城市小反刍兽疫的免疫效果,2018年6月采用横断面研究方法,对该市规模场和自然村（散养户）饲养羊只进行小反刍兽疫免疫效果评估。采用两阶段随机抽样方法,结合部分便利抽样,采集580份羊血清样品进行ELISA 抗体检测。结果显示：合格样品560份,合格率达96.5%;14个规模场均免疫合格,群体合格率达到100%;在抽检的16个自然村中,15个村免疫合格。结果表明,诸城市小反刍兽疫总体免疫效果良好。     

犊牛魏氏梭菌的分离鉴定及致病性研究

2017年1月,山东省某规模化奶牛场10～20日龄犊牛出现腹泻、拉血便、呼吸困难等症状,部分犊牛突然死亡。通过流行病学调查和尸体剖检,初步怀疑为魏氏梭菌感染。采集病料进行病理组织学检查、细菌分离鉴定、生化试验、16S及毒素基因检测等,证明疫情由A型魏氏梭菌所致。对死亡犊牛的肠内容物及分离菌株进行致病性研究,发现肠内容物及分离菌株具有较强的致病性。药敏试验结果显示,该菌对青霉素、头孢噻呋、恩诺沙星等表现极敏感。根据病原确诊情况及药敏试验结果,指导临床用药,及时控制了牛场疫情。     

农业科研院校科技档案信息化管理体系在科研绩效评价中的作用

简述农业科研院校科技档案的内涵及作用,分析农业科研院校科技档案管理存在的问题,提出构建农业科研院校科技档案信息化管理体系的建议。     

Dvl1及其突变体腺病毒载体的构建与在MSCs中表达鉴定

Dvl1及其结构缺失突变体ΔDIX（dsh and axin）和ΔDEP（dsh,Egl-10 and pleckstrin）腺病毒载体的构建并验证其在MSCs（mesenchymal stem cells）中的表达情况。将目的基因定向克隆至pAdTrack-CMV穿梭载体上,并经PmeⅠ线性化后在BJ5183细菌中与pAdEasy-1骨架质粒同源重组,获得重组腺病毒载体,在QBI-293A细胞中包装及扩增,实时荧光定量PCR和Western bolt验证Dvl1在MSCs中的表达情况。经PCR、PacⅠ单酶切鉴定及测序分析,成功构建Ad-Dvl1、Ad-ΔDIX和Ad-ΔDEP腺病毒载体,目的基因序列与GenBank报道一致,并选出150 MOI为最适感染MSCs的感染复数,成功构建了Ad-Dvl1、Ad-ΔDIX和Ad-ΔDEP腺病毒载体,并获得高滴度的病毒子,qPCR和Western blot证实Dvl1在MSCs中高表达并增加了β-catenin在细胞中的累积,为进一步研究Dvl1在MSCs迁移过程的作用奠定了基础。     

两个宁夏枸杞品种的耐渗透胁迫和耐盐特征比较

以宁夏枸杞(Lycium barbarum)中的两个品种扁果枸杞和宁杞0702为材料,对比二者在渗透胁迫、盐处理以及渗透胁迫和盐处理互作条件下的生长特征、叶组织含水量以及各器官Na~+、K~+积累量分析。结果表明,与对照相比,-0.5 MPa渗透胁迫下,扁果枸杞和宁杞0702的生长均受到抑制,其鲜重分别降低了34%和38%,根长分别降低了32%和17%;与对照相比,50mmol·L~(-1) NaCl使扁果枸杞幼苗的鲜重显著增加了38%(P0.05),干重、株高和根长均不受影响,但宁杞0702幼苗鲜重、干重、株高和根长分别显著降低了27%、34%、44%和14%(P0.05);渗透胁迫~+盐处理下,扁果枸杞幼苗与对照组差异不显著(P0.05),而宁杞0702幼苗的鲜重、干重、株高和根长分别显著降低了37%、28%、44%和13%。与对照相比,渗透胁迫下,扁果枸杞叶组织含水量维持稳定,而宁杞0702显著降低了12%(P0.05);在盐处理下,扁果枸杞和宁杞0702叶组织含水量分别显著增加了25%和18%(P0.05),在渗透胁迫~+盐处理下二者均维持稳定。在扁果枸杞中,鲜重和叶组织含水量与叶、茎中Na~+浓度呈极显著正相关(P0.01),而在宁杞0702中,鲜重仅与叶中的K~+浓度极显著正相关(P0.01),与茎中的Na~+则呈显著负相关(P0.05),叶组织含水量则与各器官中的Na~+、K~+浓度均不相关。与对照相比,扁果枸杞在渗透胁迫和盐处理下ST值分别显著增加了84%和43%(P0.05),而宁杞0702则分别显著降低了63%和47%(P0.05)。上述结果表明,扁果枸杞能通过体内积累适量的Na~+,调控体内Na~+、K~+平衡,改善体内的水分状况,维持其正常的生长,具有盐生植物的特点;宁杞0702则不具备这些特征。