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Purification of Aminopeptidase N Protein and Differences in cDNAs Encoding APN1 Between Susceptible and Resistant Helicoverpa armigera Strains to Bacillus thuringiensis Toxins 被引量:7
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作者 LIANGGe-mei WANGGui-rong +2 位作者 xuguang WUKong-ming GUOYu-yuan 《Agricultural Sciences in China》 CAS CSCD 2004年第6期456-467,共12页
The brush border membrane vesicles (BBMVs) in midgut of Helicoverpa armigera weresuccessfully separated, and most of the Aminopeptidase N (APN) activities in BBMV werepreserved. The 3-[(3-chlor-amidopropyl) dimethylam... The brush border membrane vesicles (BBMVs) in midgut of Helicoverpa armigera weresuccessfully separated, and most of the Aminopeptidase N (APN) activities in BBMV werepreserved. The 3-[(3-chlor-amidopropyl) dimethylammonio]-1-propane-sulphonate (CHAPS)can enhance the dissolution of BBMV, and phosphatidylinositol-specific phosopholipase C(PI-PLC) can cleave the APN from midgut membrane. The APN was primarily purified usinga Mono-Q column. The results of immunoblotting showed that the 120 and 170kDa proteinsin the BBMV could bind Cry1Ac, and 120kDa APN was a glycosylphosphalidylinositol(GPI)-anchored protein. Two Bt-resistant strains (Bt-P, Bt-M) were obtained after beingselected for more than five years in laboratory using Bt insecticides and Bt transgeniccotton incorporated into diet separately. The resistance of Bt-P and Bt-M were 1083.3and 48.7 times that of susceptible strain. The genes encoding APN1 in midgut ofsusceptible and resistant H.armigera were cloned by PCR and RACE techniques. Theinferred amino acid sequences of APN1 possessed the common character of APN family ininsects. In comparison with APN1 in susceptible strain, three nucleotide mutations wereobserved in the APN1 of Bt-M strain and resulted in two amino acid replace in theputative protein sequences, and eight nucleotide mutations were observed in Bt-P strainand resulted in five amino acid replace. 展开更多
关键词 Helicoverpa armigera Bt receptor protein APN1 Resistance
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Double-Differential Cross Section of ^5He Emission
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作者 YANYu-Liang DUANJun-Feng +1 位作者 ZHANGJing-Shang xuguang 《Communications in Theoretical Physics》 SCIE CAS CSCD 2005年第2期299-304,共6页
The probability of 5He particle emission has been affirmed theoretically [J.S. Zhang, Science in China G47 (2004) 137]. In order to describe the 5He emission, the theoretical formula of the double-differential cross s... The probability of 5He particle emission has been affirmed theoretically [J.S. Zhang, Science in China G47 (2004) 137]. In order to describe the 5He emission, the theoretical formula of the double-differential cross section of emitted 5He is to be established. Based on the pick-up mechanism, used for calculating the formula of d, t, 3He, α emissions, the theoretical formula of double-differential cross section of 5 He is obtained, which is expressed in the form of Legendre coefficients. In the case of low incident energies, the configuration [J.S. Zhang, Science in China G47 (2004)137; J.S. Zhang, Commun. Theor. Phys. (Beijing, China) 39 (2003) 83] is the dominant part in the reaction processes.The calculated result indicates that the forward peaked angular distribution of the composite particle emission is weaker than that of the emitted single nucleon due to pick-up nucleon from the Fermi sea. As an example, the reactions of n + 14N have been calculated, and the Legendre coefficients of d, t, 3He, α, 5He emissions are obtained respectively.The results show that the forward tendency is decided by the average momentum per nucleon in the emitted composite particles. The larger the average momentum is, the stronger the forward tendency is. 展开更多
关键词 双重微分 横截面 ^5氦原子核喷射 中子 核反应模型
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白细胞介素-7对巨噬细胞分化形成破骨细胞的影响 被引量:2
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作者 沈作佳 毛建华 +2 位作者 徐广 冉强 万锐杰 《中国中医骨伤科杂志》 CAS 2019年第7期6-9,14,共5页
目的:白细胞介素-7(IL-7)在类风湿关节炎骨破坏过程中具有重要作用,然而IL-7的具体作用方式不明确,因此本研究分析了IL-7对破骨细胞分化形成的作用及相关分子机制。方法:用M-CSF,M-CSF+RANKL及IL-7分别诱导RAW264.7巨噬细胞分化形成破... 目的:白细胞介素-7(IL-7)在类风湿关节炎骨破坏过程中具有重要作用,然而IL-7的具体作用方式不明确,因此本研究分析了IL-7对破骨细胞分化形成的作用及相关分子机制。方法:用M-CSF,M-CSF+RANKL及IL-7分别诱导RAW264.7巨噬细胞分化形成破骨细胞,通过抗酒石酸酸性磷酸酶(TRAP)染色评价IL-7对破骨细胞分化形成的影响。然后使用JAK信号通路抑制剂(AG490),AKT信号通路抑制剂(LY294002)和JNK信号通路抑制剂(SP600125),采用RT-PCR和ELISA分别检测IL-7对破骨细胞骨溶性相关活性基因和蛋白分泌的影响。最后使用蛋白印迹检测探讨IL-7促进破骨细胞分化形成的相关分子机制。结果:IL-7在核因子κB配体(RANKL)不存在的情况下能够显著增加破骨细胞的数量。IL-7能够显著诱导破骨细胞溶骨相关活性成分包括基质金属蛋白酶-9(MMP9)、组织蛋白酶(CathK)、抗酒石酸酸性磷酸酶(TRAP)、降钙素受体(CTR)的基因表达和蛋白分泌,JAK(AG490)和JNK(SP600125)信号通路抑制剂能显著抑制IL-7诱导的上述基因表达和蛋白分泌。IL-7显著诱导JAK,AKT及JNK信号通路信号蛋白的活化。结论:IL-7能不依赖于RANKL诱导破骨细胞的分化形成,其作用可能是通过活化JAK和JNK信号通路实现的。 展开更多
关键词 白细胞介素-7 破骨细胞 巨噬细胞 信号通路
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