鼠源细胞TaqMan实时荧光定量PCR检测方法的建立     

苏佳  赵炜  秦义娴  邓永  高月异  白洪旭  薛青红  陈晓春  吴华伟 《中国兽药杂志》2023,57(3):10-16

为对鼠源细胞进行鉴别检测,以鼠线粒体16S rRNA基因序列为靶位点设计特异性引物及探针,建立实时荧光定量PCR检测方法,并评价该方法的特异性及敏感性。结果显示,所建立的检测方法特异性好,针对鼠源细胞基因组荧光定量PCR扩增曲线良好,其他物种来源细胞基因组及生物制品原辅材料未出现特异性扩增曲线;敏感性高,基因拷贝数检出限度为45.3拷贝。本试验建立的荧光定量PCR检测方法能够有效地对鼠源细胞进行快速检测,为细胞质量控制提供了有效方法。  相似文献   

Biodegradation of Linear Alkyl Benzene Sulphonate     

XIANG Li-jun  WANG Bo-chu  DUAN Chuan-ren  LIU Liu  WANG Qing-hongnistry of Education  College of Bioengineering  Chongqing University  Chongqing  Chin 《保鲜与加工》2004,(10):71-74

The paper researches on the degradation of LAS (Linear Alkyl benzene Sulphonate) by combining AS1.860 immobilized with low intensity ultrasonic irradiation. The paper also discusses the influence of pH, rotary velocity, LAS concentration and the condition of low intensity ultrasonic irradiation on the degradation of LAS, the degradation rate of LAS is the main index of our experiment, the results of orthogonal test shows that low ultrasonic irradiation can increase the metabolizing of microorganism cells and facilitate the biodegradation of immobilized cells to LAS, here we research the degradation condition of 50mg/L LAS simulation wastewater with low ultrasonic irradiation, and the results show that the influence is obvious, the optimization degradation rate is about 83%, nine point five percent higher than that of the immobilized cells without ultrasonic irradiation.  相似文献   

内毒素对肠黏膜微血管内皮细胞内分泌一氧化氮和内皮素的影响   总被引：1，自引：1，他引：1  

王新  谭建华  刘金玲  韦旭斌  穆祥 《中国农学通报》2006,22(1):4-4

目的是研究内毒素（lipopolysaccharide; LPS）导致肠黏膜微血管内皮细胞损伤的作用机制。将所培养的肠黏膜微血管内皮细胞分为空白对照组和LPS组，每组按时间分为4个亚组：3h、6h、9h、12h。空白对照组加维持培养液，LPS组加1μg/ml LPS培养液，在CO2培养箱内静置培养。结果表明，一氧化氮（NO）分泌明显升高，3h后达到高峰，随后逐渐降低，而内皮素（endothelin; ET）分泌急剧升高，9h后达到高峰，随后又开始逐渐降低，但一直保持在较高的水平。所以引起了NO和ET的升高可能是LPS导致肠黏膜微血管内皮细胞的损伤机制。  相似文献   

Estrogen treatment enhances mesenteric lymphatic contractility in rats after hemorrhagic shock     

ZHANG Li-min  FENG Niu-niu  ZHAO Chen  ZHANG Yu-ping  NIU Chun-yu  ZHAO Zi-gang 《园艺学报》2021,37(1):66-71

AIM To investigate the effects of 17β-estradiol （E2） treatment on the mesenteric lymphatic microcirculation and isolated lymphatic contractility in rats after hemorrhagic shock, and to explore the relationship between contractility and the difference between intra- and extracellular calcium ion concentrations （［Ca²⁺］） of lymphatic smooth muscle cells （LSMCs）. METHODS Male Wistar rats were divided into sham group, shock group and shock+E2 group. The rats were subjected to hemorrhage ［（40±2） mmHg for 90 min］ and resuscitation with or without subcutaneous injection of E2 （2 mg/kg）. After resuscitation for 3 h, the mesenteric lymphatic microcirculation in vivo was observed. Moreover, the isolated mesenteric microlymphatic rings were prepared for the observations of lymphatic contractility evaluated by the indexes including end-systolic diameter, end-diastolic diameter, contraction frequency （CF） and passive diameter. Meanwhile, the difference between intra- and extracellular ［Ca²⁺］ of LSMCs was recorded during lymphatic contraction. RESULTS Treatment with E2 significantly enhanced the CF, total contractile fraction and lymphatic dynamics index in vivo in the rats after hemorrhagic shock, and increased the CF, the fractional pump flow and the difference between intra- and extracellular ［Ca²⁺］ of LSMCs in isolated lymphatics from the shocked rats （P<0.05）. CONCLUSION Estrogen treatment enhances lymphatic contractility in rats after hemorrhagic shock, which is related to enhancement of difference between intra- and extracellular ［Ca²⁺］ of LSMCs.  相似文献   

Role of miR-30b in calcification of rat vascular smooth muscle cells induced by high phosphorus     

ZHOU Wei  XU Jin-sheng  BAI Ya-ling  ZHANG Hui-ran  HE Lei  ZHANG Sheng-lei  ZHANG Dong-xue 《园艺学报》2021,37(1):54-59

  相似文献   

Physiological and pathological roles of mast cells in adipose tissue     

QI Rui-juan  GAO Yuan  QI Yun 《园艺学报》2021,37(1):151-158

Mast cells are important cells for the innate immunity that reside in tissues including adipose tissue and are involved in various physiological and pathological processes by producing a range of biological mediators. Adipose tissue not only acts as an energy depot and regulator of energy homeostasis that can deposit excess energy and dissipate energy through heat, but also is an active endocrine organ capable of producing hormones and adipokines. The dysfunction of adipose tissue is highly correlated with metabolic disorders, such as obesity, type 2 diabetes mellitus and so on. This review focuses on the physiological and pathological roles of mast cells in adipose tissue.  相似文献   

Construction of mouse ESC line stably expressing Pdx1 by Tet-On system     

ZHONG Wa  XIA Zhong-sheng  YU Tao  NI Chu-yan  LI Jie-yao  CHEN Qi-kui 《园艺学报》2021,37(1):187-192

AIM To construct the mouse embryonic stem cell （ESC） line with stable pancreatic and duodenal homeobox 1 （Pdx1） expression by Tet-On system, which may lay a foundation for further research on the differentiation of Pdx1⁺ definitive endoderm cells into pancreatic cells. METHODS The Pdx1-overexpressing lentiviral vector with green fluorescent protein marker and puromycin resistance was constructed by Tet-On system and was used to infect the mouse ESC. The cells were divided into 3 groups： blank control group （ESC group）, empty lentivirus control group （PDX1^- ESC group） and Pdx1 lentivirus transfection group （PDX1⁺ ESC group）. Flow cytometry was used to detect the transfected cells after screening by doxycycline （DOX）. The function of Tet-On system and the expression of Pdx1 gene were detected. The transfected cells in PDX1^- ESC group and PDX1⁺ ESC group were sorted by flow cytometry, and constructed ESC line with stable expression of Pdx1 and negative control ESC line were verified. RESULTS （1） The positive rates of transfected cells in PDX1^- ESC group and PDX1⁺ ESC group were 90.72% and 94.01% after screening by DOX, respectively. The positive rates of transfected cells in PDX1^- ESC group and PDX1⁺ ESC group was 97.84% and 98.13% after sorting by flow cytometry, respectively. （2） With DOX, green fluorescence was observed in PDX1^- ESC group and PDX1⁺ ESC group. The mRNA and protein expression of Pdx1 was significantly increased in PDX1⁺ ESC group （P<0.05）. Without DOX, no green fluorescence was observed in the cells of the 3 groups, and no significant difference in the mRNA and protein expression of Pdx1 was observed （P>0.05）. （3） After 3 months of cryopreservation, the cell lines still survived in resuscitation culture and were regulated by DOX. CONCLUSION Using Tet-On system, the mouse ESC line with inducible Pdx1 expression were successfully established and could be used as an effective cell model to research the differentiation of Pdx1⁺ definitive endoderm cells into pancreatic cells.  相似文献   

寡齿新银鱼卵细胞粘丝的亚显微结构     

龚世园  严国璋 《华中农业大学学报》1996,15(5):459-462,T001

经电镜扫描寡齿新银鱼的第Ⅳ时相，第Ⅴ时相卵母细胞和受卵的卵细胞粘丝，结果表明，卵细胞表面具从受精孔发生的１２根左右粘丝，此粘丝于受精孔处微弱弯曲，经侧部渐向受精孔相对处呈现很强扭曲或互相缠绕。卵细胞粘丝不仅出现在受精卵和第Ⅴ时相卵母细胞表面，而且清晰地出现在第Ⅳ时相卵母细胞的滤泡膜上。  相似文献   

大银鱼卵细胞粘丝扫描电镜观察   总被引：1，自引：0，他引：1  

龚世园  梁开学 《华中农业大学学报》1996,15(6):580-583,T002

用扫描电镜观察了大银鱼的第Ⅲ时相，第Ⅳ时相，第Ⅴ时相卵母细胞和受精卵的卵细胞粘丝的外部形态特征和它们的粘性，并讨论了卵细胞粘丝的功能。  相似文献   

支持细胞中促卵泡素信号通路研究进展   总被引：4，自引：1，他引：3  

高小燕  孙燕  张家骅 《动物医学进展》2006,27(5):1-5

支持细胞在精子生成过程中起重要作用,支持细胞的数量决定睾丸大小、生精细胞数量以及最终生成精子数量。促卵泡素作为保证雄性生育能力的重要激素之一,通过与支持细胞上的促卵泡素受体结合,诱导5种信号途径,导致支持细胞中各类转录因子被激活,引起基因表达发生变化,从而保证生精细胞顺利发育成精子。文章主要围绕支持细胞中促卵泡素信号途径,及其对细胞发育过程中相关基因表达的影响等方面进行了综述。  相似文献