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噻唑蓝3-(4,5-二甲基-2-)-2,5-二苯基溴化四唑盐(MTT)比色法是传统上检测细胞增殖和细胞毒性的常用方法.CloneSelectTM成像系统是一种以影像为基础的用于分析细胞生长的可视检测系统.本研究采用人结直肠癌HCT116细胞系,运用CloneSelect成像系统和MTT方法分别检测药物阿的平的细胞毒性,并采用Bland-Altman作图法比较两种实验方法获得的pEC50值,分析两种研究方法获得的结果的一致性.结果表明,CloneSelectTM成像系统和MTT法获得的pEC50值具有较好的一致性.与MTT方法相比,基于影像的CloneSelectTM成像分析技术检测快速、无损伤且结果更准确,获取资料不损伤细胞,允许后续其它时间点或动力学检测.研究提示,这种新的以影像为基础的检测技术可以替代MTT方法,用于分析不同药物的抗细胞增殖活性. 相似文献
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Yan-Ting Zhang Li-Hui Xu Qun Lu Kun-Peng Liu Pei-Yan Liu Fang Ji Xiao-Ming Liu Dong-Yun Ouyang Xian-Hui He 《PloS one》2014,9(4)
Cucurbitacin B (CuB), a potent antineoplastic agent of cucurbitacin triterpenoids, induces rapid disruption of actin cytoskeleton and aberrant cell cycle inhibiting carcinogenesis. However, the underlying molecular mechanism of such anticancer effects remains incompletely understood. In this study, we showed that CuB treatment rapidly induced vasodilator-stimulated phosphoprotein (VASP) phosphorylation (i.e. activation) at the Ser157 residue and generated VASP clumps which were co-localized with amorphous actin aggregates prior to the formation of highly-ordered cofilin-actin rods in melanoma cells. Knockdown of VASP or inhibition of VASP activation using PKA-specific inhibitor H89 suppressed CuB-induced VASP activation, actin aggregation and cofilin-actin rod formation. The VASP activation was mediated by cAMP-independent PKA activation as CuB decreased the levels of cAMP while MDL12330A, an inhibitor of adenylyl cyclase, had weak effect on VASP activation. Knockdown of either Gα13 or RhoA not only suppressed VASP activation, but also ameliorated CuB-induced actin aggregation and abrogated cofilin-actin rod formation. Collectively, our studies highlighted that the CuB-induced actin aggregation and cofilin-actin rod formation was mediated via the Gα13/RhoA/PKA/VASP pathway. 相似文献
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Xian-Hui Dong Dong-Xue Ma Tian-Ci Zhang Xiao-Ping He Li-Jun Xu Ya-Lei Liu Hao Li Wei-Juan Gao 《Neurochemical research》2021,46(5):1068-1080
Neurochemical Research - Alzheimer’s disease (AD) process is characterized classically by two hallmark pathologies: β-amyloid (Aβ) plaque deposition and neurofibrillary tangles of... 相似文献
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Yang XH Wen Q Zhao TT Sun J Li X Xing M Lu X Zhu HL 《Bioorganic & medicinal chemistry》2012,20(3):1181-1187
A series of cinnamic acyl 1,3,4-thiadiazole amide derivatives (6a-10e) have been designed and synthesized, and their biological activities were also evaluated as potential antiproliferation and tubulin polymerization inhibitors. Among all the compounds, 10e showed the most potent activity in vitro, which inhibited the growth of MCF-7 and A549 cell lines with IC(50) values of 0.28 and 0.52μg/mL, respectively. Compound 10e also exhibited significant tubulin polymerization inhibitory activity (IC(50)=1.16μg/mL). Docking simulation was performed to insert compound 10e into the crystal structure of tubulin at colchicine binding site to determine the probable binding model. Based on the preliminary results, compound 10e with potent inhibitory activity in tumor growth may be a potential anticancer agent. 相似文献
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Zhao TT Lu X Yang XH Wang LM Li X Wang ZC Gong HB Zhu HL 《Bioorganic & medicinal chemistry》2012,20(10):3233-3241
A series of 2,6-dinitro-4-(trifluoromethyl)phenoxysalicylaldoxime derivatives (1h-20h) have been designed and synthesized, and their biological activities were also evaluated as potential antiproliferation and tubulin polymerization inhibitors. Among all the compounds, 2h showed the most potent activity in vitro, which inhibited the growth of MCF-7, Hep-G2 and A549 cell lines with IC(50) values of 0.70 ± 0.05, 0.68 ± 0.02 and 0.86 ± 0.05 μM, respectively. Compound 2h also exhibited significant tubulin polymerization inhibitory activity (IC(50)=3.06 ± 0.05 μM). The result of flow cytometry (FCM) demonstrated that compound 2h induced cell apoptosis. Docking simulation was performed to insert compound 2h into the crystal structure of tubulin at colchicine binding site to determine the probable binding model. Based on the preliminary results, compound 2h with potent inhibitory activity in tumor growth may be a potential anticancer agent. 相似文献
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Yin CC He Y Zhou DH Yan C He XH Wu SM Zhou Y Yuan ZG Lin RQ Zhu XQ 《The Journal of parasitology》2010,96(6):1233-1234
Toxoplasma gondii is widely distributed in humans and other animals, including wild rats throughout the world, but little is known of the prevalence of T. gondii in rats in China. The seroprevalence of T. gondii in rats ( Rattus norvegicus and Rattus flavipectus ) was investigated in Guangzhou, southern China, between November 2009 and January 2010. In total, 217 rat serum samples were collected; antibodies to T. gondii were detected by the modified agglutination test (MAT), and 7 (3.2%) were found positive (titers ≥ 1:40). The seroprevalence was higher (3.4%) in R. norvegicus than in R. flavipectus (3.0%), but the difference was not statistically significant (P > 0.05). All 7 positive rats were female; no T. gondii antibodies were detected in males. This is the first extensive survey of T. gondii infection in rats in southern China, and the results have public health implications in this region. 相似文献
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T cell activation is dependent upon signals deliveredthrough the antigen-specific T cell receptors and costimula-tory molecules [1,2]. The B7 family of costimulatory mol-ecules provides signals that are critical for both stimula-ting and inhibiting T cell… 相似文献
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蝴蝶果根、果仁挥发油化学成分的研究 总被引:2,自引:0,他引:2
采用水蒸气蒸馏法从大戟科蝴蝶果的根和果仁中提取挥发油,用气相色谱-质谱联用技术对挥发油化学成分进行分析,并应用面积归一化法测定各成分的相对百分含量。从根中鉴定出23种化合物,占总油量的100%,其主要成分为十六烷酸(18.74%)、(Z,Z)9,12-十八碳二烯酸(12.81%)、1,2-苯二羧酸双(2-甲基丙基)酯(10.59%)、二丁基邻苯二甲酸酯(7.42%)及二十四烷(6.72%)。从果仁中鉴定出17种化合物,占总油量的100%,主要成分为(E-)-9-十八碳烯酸(23.15%)、正十六烷酸(21.20%)、(Z,Z)-9,12-十八碳二烯酸(19.26%)及3-甲基十七烷(6.80%)。 相似文献