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本研究克隆了中华鳖(Pelodiscus sinensis)T细胞表面标记分子CD3γ/δ、CD3ε和CD3ζ的基因,分析了其在组织/器官表达的分布,并进一步揭示了嗜水气单胞菌(Aeromanas hydrophila)感染后这些基因的表达变化。中华鳖CD3γ/δ和ε分子结构相似,均含有1个免疫球蛋白样结构的胞外区、1个跨膜区和含有1个ITAM结构域的胞浆区。与之不同的是,CD3ζ含有1个仅由10个氨基酸组成的胞外区、1个跨膜区和含有3个ITAM结构域的胞浆区。通过生物信息学分析显示,CD3γ/δ由6个外显子和5个内含子组成,CD3ε由7个外显子和6个内含子组成,且CD3γ/δ和CD3ε位于染色体Scaffold JH208224中反向排列且相距9.9 kb。CD3ζ位于染色体Scaffold JH209116.1上,由8个外显子和7个内含子组成。荧光定量PCR分析显示,CD3γ/δ、ε和ζ在脾、肝、肠、血液中表达量较高,在胸腺、肾、心脏、肌肉和肺中表达量低。腹腔注射嗜水气单胞菌12 h后,CD3γ/δ、ε和ζ在胸腺中都呈显著的上调表达,分别为对照组的69.3倍、85.7倍和163.4倍,表明细菌感染可以诱导CD3分子的表达。 相似文献
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用含复合芽孢杆菌(105cfu/g饲料,枯草芽孢杆菌和解淀粉芽孢杆菌以1∶1比例混合)的基础日粮,按体重3%的日投饵量,饲喂体重(51.37±0.58)g的草鱼(Ctenopharyngodon idellus),饲养实验45 d。结果表明:与对照组相比,处理组肠道内容物胰蛋白酶活性提高了79.46%(P<0.01);肝胰腺脂肪酶活性提高了16.82%(P<0.01),肝胰腺淀粉酶和胰蛋白酶活性无显著差异(P>0.05)。肠道菌群数量分析显示,处理组肠道芽孢杆菌数均显著提高(P<0.01),弧菌和大肠杆菌数显著降低(P<0.01)。结果提示,饵料中添加复合芽孢杆菌能够改善草鱼肠道菌群组成,并提高消化道特定消化酶活性。 相似文献
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为了考查高体鳑鲏(Rhodeus ocellatus)幼鱼的集群行为,研究选取248尾幼鱼,组成1、2、4、8和16尾高体鳑鲏幼鱼的群体(N = 8),在(25 ± 1)℃水温条件下进行15分钟的视频拍摄、运动轨迹提取和分析。结果显示:①高体鳑鲏的自发游泳速度多介于0-10 cm/s之间,其速度中位数随群体大小上升呈先下降后上升的趋势(P ﹤ 0.05),但各组间游泳速度的同步性随群体大小的上升而下降(P ﹤ 0.05);②焦点鱼和群体中其它个体的最近邻距离(NND)多出现在0-10 cm之间,且2和4个体组的NND显著大于8和(或)16个体组(P ﹤ 0.05);③2和4个体组排列的极性显著高于8和16个体组(P ﹤ 0.05)。研究结果表明群体大小对高体鳑鲏集群行为的特征有显著影响,随群体大小上升,凝聚力上升,但协调性有所下降。 相似文献
197.
IBA对芍药扦插生根的影响及生根过程中相关酶活性的变化 总被引:7,自引:1,他引:6
以芍药‘大富贵’品种为材料, 用1 000、2 000和3 000 mg·L-1 3个浓度的IBA处理进行扦插对比试验, 研究其生根过程中过氧化物酶( POD) 、多酚氧化酶( PPO) 、吲哚乙酸氧化酶( IAAO) 活性的动态变化。结果表明: IBA处理极显著地提高了插穗的生根率、根数和总根长, 其中以2 000 mg·L -1为IBA最佳生根浓度, 将生根周期缩短18 d, 并明显提高了生根质量。在生根过程中, 插穗中POD、PPO活性分别呈现“缓慢上升→下降→急剧上升→下降”和“降→升→降”的变化趋势, 但与对照组相比, 处理组的变化更为剧烈, 峰值出现提前了18 d。IAAO活性在对照和处理中呈现不同的变化趋势: 前者为“升→降→升”, 而后者为“降→降→升”。此外, 高活性的POD、PPO有利于不定根的形成, 低活性的IAAO则促进生根。 相似文献
198.
AIM: To study the effect of inhibiting nuclear factor-kappa B (NF-κB) activity on the expression of angiotensinogen (AGT) and the production of angiotensinⅡ (AngⅡ) induced by tumor necrosis factor-α (TNF-α) in glomerular mesangial cells (MCs) of SD rats. METHODS: The MCs of SD rats were isolated and divided into three groups as follows: control; MCs treated with TNF-α, and the MCs treated with TNF-α + pyrrolidinedithiocarbamate (PDTC). The activity of nuclear factor-kappa B was measured by electrophoretic mobility shift assay. The expression of AGT was determined by RT-PCR for mRNA and Western blotting for protein. The concentration of angiotensinⅡ in supernatant was measured by RIA. RESULTS: The NF-κB activity in the MCs treated with TNF-α (20.67±9.14)×102 μg/cell was significantly higher than that in control cells [(8.25±4.35)×102 μg/cell, P<0.01] and the MCs treated with TNF-α+PDTC [(7.20±4.57)×102 μg/cell, P<0.01], and no significant difference was found between control and the MCs treated with TNF-α+PDTC (P>0.05). The AGT mRNA level in the MCs treated with TNF-α (0.27±0.05) was higher than that in the control cells (0.20±0.05, P<0.05), and no significant difference was observed when compared with that in the MCs treated with TNF-α+PDTC (0.22±0.06, P>0.05). The expression of AGT protein in the MCs treated with TNF-α (0.60±0.19) μg/cell was higher than that in the control [(0.37±0.15)μg/cell, P<0.05] and the MCs treated with TNF-α+PDTC [(0.37±0.17)μg/cell, P<0.05], and no significance was found between the MCs treated TNF-α+PDTC and the control (P>0.05). The AngⅡ level in supernatant of cultured MCs treated with TNF-α [(9.73±2.38)×10-5 ng·L-1/cell] was significantly higher than that in the control [(7.50±1.51)×10-5 ng·L-1/cell, P<0.05] and in the MCs treated with TNF-α+PDTC [(6.94±1.46)×10-5 ng·L-1/cell, P<0.05], however, the difference between the MCs treated with TNF-α+PDTC and the control was of no significance (P>0.05). CONCLUSION: TNF-α activates the NF-κB in glomerular MCs, induces the AGT expression and the production of AngⅡ. Inhibition of NF-κB decreases the AGT expression and the production of AngⅡ. Therefore, the effects of TNF-α on AGT and AngⅡ may be mediated by NF-κB. 相似文献
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200.
WAN Jian-xin GUO Qi WANG Jing-han PAN Yang-bin CUI Jiong FU Bin-bin XU Yan-fang 《园艺学报》2009,25(8):1628-1634
AIM: To observe the effects of cytokines on renovation of acute renal failure (ARF) in mouse with bone marrow derived mesenchymal stem cell (MSC) transplantation. METHODS: ARF animal model was induced in mouse by subcutaneous injection of cisplatin. Mice were randomly assigned into 3 groups: normal control group, ARF group and MSC group. After 24 h cisplatin injection, animals were injected intravenously with MSC in MSC group. Animals were sacrificed at 1 d, 4 d, 7 d, 14 d and 28 d after cisplatin injection. The blood urea nitrogen (BUN) and serum creatinine (Scr) were measured. The renal morphologic changes were scored with Paller’s criterion on hematoxylin and eosin (HE) stained sections. The mRNA and protein expressions of HGF, BMP-7, TNF-α and IL-10 were detected by RT-PCR and immunohistochemistry method. RESULTS: After 4 d of cisplatin injection, the BUN and Scr values in MSC group were significantly lower than those in ARF group (P<0.01). After 7 d and 14 d, the values of BUN and Scr in MSC group were still lower than those in ARF group (P<0.01, P<0.05). The renal morphologic scores of MSC group were also lower than those of ARF group. After 7 d, the expressions of HGF, BMP-7 and IL-10 were higher in MSC group than those in ARF group, the expression of TNF-α in MSC group was lower than that in ARF group. CONCLUSION: MSC promotes the recovery of acute renal failure induced by cisplatin. The mechanism may partly depend on paracrine of growth factor and amelioration of inflammatory. 相似文献