团头鲂IL-12表达及功能的初步研究     

武佳琪  王济秀  刘红 《水产学报》2022,46(11):2028-2037

白细胞介素-12（IL-12）是一种连接先天性和适应性免疫系统的重要细胞因子,在免疫反应和炎症反应中均发挥着重要作用。本实验以团头鲂为研究对象,克隆了团头鲂IL-12的4个亚基IL-12A、IL-12Ba、IL-12Bb和IL-12Bc的开放阅读框（ORF）序列,长度分别为588、993、939和837 bp。实时荧光定量PCR（RT-qPCR）结果表明,团头鲂IL-12各亚基在检测的10个不同的成鱼健康组织中都有表达,但是在不同组织中的表达模式不同;腹腔注射嗜水气单胞菌后,团头鲂IL-12各亚基在免疫相关组织中显著差异表达;脂多糖（LPS）刺激分离的团头鲂头肾淋巴细胞后,4个IL-12亚基均被快速诱导表达。进一步通过大肠杆菌原核表达系统和变性复性方法得到团头鲂IL-12Bb、IL-12Bc重组蛋白并刺激分离的头肾淋巴细胞,显著上调TNF-α、IL-1β、IFN-γ的表达,表明获得的重组蛋白具有生物学活性。最后对获得的蛋白进行抑菌活性检测,结果表明重组IL-12Bb、IL-12Bc单体蛋白对嗜水气单胞菌、大肠杆菌和金黄色葡萄球菌都有明显的抑制作用。综上,本研究结果表明,团头鲂IL-12在调节免疫应答的过程中发挥着重要作用。  相似文献   

Establishment of a Conditional Transgenic System Using the 2A Peptide in the Female Mouse Germline     

Satoshi HARA  Takashi TAKANO  Mio OGATA  Reina YAMAKAMI  Yusuke SATO  Tomohiro KONO  Yayoi OBATA 《The Journal of reproduction and development》2014,60(3):250-255

Transgenic mice are essential research tools in developmental biology studies. The 2A peptide allows multiple genes to be expressed simultaneously at comparable levels in somatic cells, but there are no reports of it being used successfully in germ cells. We constructed a Cre/loxP-based conditional vector containing the 2A peptide to significantly enhance the expression of a reporter and target gene from a constitutive promoter in oocytes. Mice with a transgene insertion containing the chicken β-actin promoter, floxed EGFP-polyA cassette, mCherry reporter, 2A peptide and target gene DNA methyltransferase 3A2 (Dnmt3a2) were crossed with TNAP- or Vasa-Cre mice to produce offspring, in which mCherry and DNMT3A2 proteins were highly expressed in oocytes upon Cre-mediated removal of EGFP-polyA. This novel transgenic mouse line based on the 2A expression system can serve as a useful tool for examining gene function during oogenesis.  相似文献   

PRRSV特异性肽对CSF、PRRS免疫猪IFN-Y、IL-10分泌的影晌     

郎广平  郭敏  梁志选  冯娇  孔惟博  任少敏  李彬  韩盈盈  赵建增  高英杰 《兽医大学学报》2014,(2):187-191

应用PRRSV-GP5特异性肽刺激CSF、PRRS免疫猪外周血淋巴细胞,采用EI。IsA方法测定不同时间点淋巴细胞分泌IFN-7及IL-10的水平,分析PRRSv_GP5特异性肽刺激后,淋巴细胞培养上清中细胞因子的变化规律。结果显示,CSFV高抗PRRSV低抗体组于PRRSV免疫14d,肽刺激组中IFN-7水平显著高于对照组（P〈0．05）;其他组均差异不显著（P〉0．05）。PRRSV免疫14d,细胞培养24,72h后加PRRSV—GP5肽刺激,各组中试验组与对照组相比IL-10水平明显降低（P〈0．01）;PRRSV免疫28d,各组中肽刺激组与空白组相比,IL-10水平均无显著性差异（P〉0．05）。结果表明,PRRSV-GP5肽在PRRSV免疫早期可以促进IFN-7的分泌,并抑制IL-10的产生,但在免疫后期对淋巴细胞分泌的调节作用还需进-步研究。  相似文献   

大口黑鲈不同组织中抗菌肽粗提及抑菌活性测定     

董晓庆  张东鸣 《中国兽药杂志》2014,48(6):8-11

研究了大口黑鲈不同组织中抗菌肽的提取及其粗提物对不同菌种的抑菌作用。以新鲜的大口黑鲈为试验材料,用5％乙酸作为提取液,对大口黑鲈粘液、皮肤、肝脏、脾、卵、鳃组织进行提取,并对粗提物进行抑菌活性检测。结果表明大口黑鲈粘液、皮肤和肝脏组织提取物对嗜水气单胞菌有抑菌作用,皮肤和肝脏组织提取物对大肠杆菌有抑菌作用。肝脏组织抗菌肽提取物经SephadexG-25凝胶过滤层析柱分离后,其收集液对嗜水气单胞菌仍具有抑菌作用。大口黑鲈皮肤和肝脏组织提取物对嗜水气单胞菌、大肠杆菌均有抑菌作用。  相似文献   

广西巴马小型猪GHRH成熟肽真核表达质粒对小鼠生长效应的影响     

李芳芳  ;郭亚芬  ;兰干球  ;潘堂峰 《广西农业科学》2014,(12):2264-2269

【目的】探讨广西巴马小型猪促生长激素释放激素（GHRH）成熟肽真核表达质粒对小鼠生长效应的影响,为进一步研究广西巴马小型猪GHRH成熟肽的促生长作用及GHRH基因疫苗的高效制备与安全使用提供参考依据。【方法】利用基因重组技术将广西巴马小型猪GHRH成熟肽序列与p EGFP-N1质粒连接构建重组真核表达质粒,然后按0.5μg/g的剂量肌肉注射经25%蔗糖溶液预处理的小鼠,观察记录小鼠体重变化情况,并分别提取重组质粒注射组小鼠的心脏、肝脏、肾脏及注射部位肌肉DNA,再以PCR检测是否存在基因质粒残留。【结果】以构建的p EGFP-GHRH重组质粒注射小鼠后,其外源GHRH成熟肽DNA可在肌肉中获得表达,但并未整合入小鼠基因组中。虽然重组质粒注射组小鼠的末重与空质粒注射组小鼠的差异不显著（P〉0.05）,但在注射后的10-25 d,重组质粒注射组小鼠体重均显著高于空质粒注射组（P〈0.05）。在相对日增重率方面,注射后的前15 d内,重组质粒注射组小鼠的相对日增重率均高于空质粒注射组。【结论】构建的广西巴马小型猪p EGFP-GHRH重组质粒能在一定时间内促进小鼠生长,即GHRH种属差异性小,在动物中有较高的保守性。  相似文献   

小肽营养研究进展   总被引：1，自引：0，他引：1  

胡佐忠  陈红跃 《畜禽业》2007,(9):12-15

小肽(sp)是动物降解蛋白质为氨基酸过程中的中间产物,对动物的重要营养有重要的营养作用。本文就小肽的吸收机制和特点、影响小肽释放和吸收的因素、小肽的营养作用以及其在动物营养中的应用等作一综述。  相似文献   

Treatment of the early life stages of scallop (Pecten maximus) with antimicrobial agents; searching for an alternative to chloramphenicol     

Lise Torkildsen  Rosie Coyne  Ole Bent Samuelsen  Thorolf Magnesen  Øivind Bergh 《Aquaculture International》2002,10(5):399-409

High mortality rates are often observed in rearing the early stages of the great scallop, Pecten maximus. The addition of antibacterial agents has been necessary to improve larval survival. However, as one antibacterial agent, chloramphenicol, is banned in Norway and Europe the aim of this study is to investigate alternative antibacterial agents. The therapeutic agents investigated in this study were florfenicol, oxytetracycline, oxolinic acid, neomycin and Pyceze. The mean minimum inhibitory concentration (MIC) values were determined for oxytetracycline, oxolinic acid and Pyceze against bacteria isolated from scallop larvae. Two types of treatment regime were investigated on an intermediate scale (20 L). One regime involved continuous exposure of scallop larvae to the therapeutic agent while the other involved a short exposure lasting two hours. All intermediate scale treatments were performed in parallel to large-scale production (800 L) treatment with chloramphenicol. Of the therapeutants investigated, oxolinic acid was the most effective, although only at high concentrations. The short exposure of two hours was ineffective for all therapeutics.  相似文献   

Natriuretic peptide inhibition of intestinal salt absorption in the Japanese eel: physiological significance   总被引：2，自引：0，他引：2  

C.A. Loretz  C.A. Loretz  Y. Takei 《Fish physiology and biochemistry》1997,17(1-6):319-324

Electrophysiological studies in vitro demonstrated the significant inhibition by natriuretic peptides (NP) of short-circuit current across the eel intestine, an important osmoregulatory organ. Inhibitory potencies of several members of the NP family were assessed by voltage-clamp determination of net transepithelial salt absorption measured as the short-circuit current I_sc across the intestine of the freshwater-adapted (FW) and seawater-adapted (SW) Japanese eel (Anguilla japonica); the order of potency of synthetic eel peptides was: amidated atrial natriuretic peptide (ANP-NH₂) > ventricular natriuretic peptide (VNP) > atrial natriuretic peptide (ANP) >> C-type natriuretic peptide (CNP). Neither the order of potency nor the absolute potencies were effected by salinity adaptation. The observed potency sequence suggests that inhibition of intestinal absorption is mediated by A-type guanylyl cyclase-coupled NP receptors. The relatively low sensitivity of the intestinal response to NP compared with circulating NP concentrations suggests a role for intestinal regulation by NP which is independent of systemic delivery from cardiac sources. A novel model, incorporating the known immunohistochemical localization of NP-ergic cells and processes in the epithelial layer of the intestine and the dissipation of the Na⁺ electrochemical gradient along the alimentary tract, is developed in which local secretion of NP (in response to a bolus of food) inhibits salt absorption across the intestine regionally in favor of increased nutrient absorption.  相似文献   

海洋贝类体液防御机制的研究进展   总被引：3，自引：0，他引：3  

杨明  侯敢  黄迪南  李江滨 《水产科学》2006,25(8):428-430

近几年，随着人们将海洋贝类作为食物的兴趣日益浓厚，科学家们对贝类及其防御机制的研究也越来越深入，对它们在生态、社会、经济、营养等方面的作用以及它们的致病微生物的特性进行了大量研究。双壳贝类由于其滤食习性，使它们体内蓄积了大量细菌，成为人类致病菌的积极携带者。因此，研究贝类与微生物之间的相互作用对维护人类健康有重要意义。  相似文献   

Biochemistry and physiology of a family of eel natriuretic peptides   总被引：1，自引：0，他引：1  

Yoshio Takei  Richard J. Balment 《Fish physiology and biochemistry》1993,11(1-6):183-188

Three natriuretic peptides with similar structures were isolated from eels and their amino acid sequences determined; atrial natriuretic peptide (ANP) from atria, ventricular natriuretic peptide (VNP) from ventricles, and C-type natriuretic peptide (CNP) from brains. All three hormones were circulating in eel blood, and their plasma levels invariably decreased when eels were transferred from fresh water (FW) to seawater (SW). Eel ANP and VNP inhibited drinking in FW and SW eels. Eel ANP inhibited water and Na⁺ absorption by the intestine of SW eels. The potency of these ANP effects was 2–3 orders greater than those of other hormones which are known to have similar effects. Eel ANP and VNP induced antidiuresis but not antinatriuresis in FW eels. Eel ANP increased plasma cortisol level in SW eels but not in FW eels. The antidiuretic effect and the stimulation of cortisol secretion in eels are opposite to the ANP effects reported in mammals. These data suggest that ANP plays a complex role in the eel osmoregulation.

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Résumé Trois peptides natriurétiques présentant des structures similaires ont été isolés chez l'anguille et leurs séquences en acides aminés a été déterminées; le peptide atrial natriurétique (ANP) dans l'atria, le peptide ventriculaire natriurétique (VNP) dans les ventricules et le peptide natriurétique de type C dans le cerveau. Ces trois hormones sont présents dans le sang d'anguille et leur niveau plasmatique decroit invariablement quand les anguilles sont transférées d'eau douce en eau de mer. L'ANP et le VNP d'anguille inhibent l'action de boire chez les anguilles d'eau douce et d'eau de mer. L'ANP d'anguille inhibe l'absorption d'eau et de Na⁺ par l'intestin d'anguille en eau de mer. Ces effets de l'ANP sont 2 à 3 fois plus grands que ceux observés avec d'autres hormones qui sont connues pour avoir des effets similaires. L'ANP et le VNP d'anguille induisent l'antidiurèse mais pas l'antinatriurèse chez les anguilles d'eau douce. L'ANP d'anguille augmente chez ce poisson les niveaux de cortisol plasmatique en eau de mer mais pas en eau douce. L'effet antidiurétique et la stimulation de la sécrétion de cortisol chez l'anguille sont contraire aux effets de l'ANP observés chez les mammifères. Ces résultats suggèrent que l'ANP joue un role complexe dans l'osmorégulation de l'anguille.

  相似文献