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Effect of Icariin on apoptosis and expression of Fas,Fas ligand,B cell lymphoma,and Bcl-2-associated X protein in CD4+ T lymphocytes from patients with ankylosing spondylitis 被引量:2
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作者 Wang Hailong Jiang Quan Feng Xinghua 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2017年第2期207-213,共7页
OBJECTIVE:To investigate the effects of icariin on apoptosis and the expression of Fas, Fas ligand(Fas L), B cell lymphoma(Bcl-2), and Bcl-2-associated X protein(Bax) in CD4+ T lymphocytes from patients with ankylosin... OBJECTIVE:To investigate the effects of icariin on apoptosis and the expression of Fas, Fas ligand(Fas L), B cell lymphoma(Bcl-2), and Bcl-2-associated X protein(Bax) in CD4+ T lymphocytes from patients with ankylosing spondylitis.METHODS:Primary cultures of peripheral blood CD4+ T lymphocytes were established and treated with icariin at high, medium, and low doses(0.5,0.25, and 0.125 mg/mL).Sulfasalazine treated and helthy cells were used as controls.Apoptosis of treated cells was determined by flow cytometry.Reverse transcription polymerase chain reaction and enzyme-linked immunosorbent assays were used to determine the effects of icariin on the expression of Fas, Fas L, Bcl-2, and Bax.The activity of caspase 8 and caspase 3 was determined by a colorimetric assay.RESULTS:The m RNA and protein expression of Fas,and activity of caspase 8 and caspase 3 in CD4+ T lymphocytes were increased by icariin(P < 0.05).Conversely, the m RNA and protein expression of Bcl-2 was decreased(P < 0.05).The expression of Fas L and Bax were not significantly different between groups.The proapoptotic effects of icariin were dose-dependent.CONCLUSION:Icariin induces the apoptosis of CD4 + T cells from patients with AS comparing to normal control.Therefore, the induction of apoptosis may be the likely mechanism of action of icariin's antirheumatics activities. 展开更多
关键词 SPONDYLITIS ANKYLOSING FAS Fas Ligand protein Lymphoma B-Cell bcl-2-associated X protein CD4-positive T-lymphocytes APOPTOSIS ICARIIN
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BAG2对蛋白酶体抑制剂诱导人甲状腺癌细胞凋亡作用影响的观察
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作者 王玉林 王彪 +1 位作者 孟欣 巴颖 《中国癌症杂志》 CAS CSCD 北大核心 2014年第5期349-353,共5页
背景与目的:蛋白酶体抑制剂对不同组织来源的肿瘤均有抑制其增长和促进细胞凋亡的作用,其作用机制可能与Bcl-2相关抗凋亡基因2(Bcl-2-associated athanogene 2,BAG2)有关,本研究探讨BAG2在蛋白酶体抑制剂诱导甲状腺癌细胞凋亡中... 背景与目的:蛋白酶体抑制剂对不同组织来源的肿瘤均有抑制其增长和促进细胞凋亡的作用,其作用机制可能与Bcl-2相关抗凋亡基因2(Bcl-2-associated athanogene 2,BAG2)有关,本研究探讨BAG2在蛋白酶体抑制剂诱导甲状腺癌细胞凋亡中的作用。方法:选取人甲状腺未分化癌细胞系ARO、FRO、KTC1、KTC2、KTC3、8305C和8505C,分别设培养液处理空白对照组、蛋白酶体抑制剂MG132处理组;利用实时定量逆转录聚合酶链反应(quantitative real-time polymerase chain reaction,qRT-PCR)检测各组细胞BAG2 mRNA表达及MG132诱导其表达的时效性;利用蛋白质印迹法(Western blot)检测各组细胞BAG2蛋白表达。结果:MTT结果显示,FRO和KTC2细胞系对蛋白酶体抑制剂最为敏感,与空白对照组相比,MG132能不同程度的增加各种细胞BAG2 mRNA及蛋白的表达水平(P〈0.01),在FRO和KTC2细胞中,BAG2 mRNA水平较对照组增加20-25倍,蛋白质的表达水平也显著增加;时间效应实验中,敏感的FRO细胞BAG2 mRNA水平增加快,没有延迟期;并且增加的最高水平显著高于非敏感的ARO细胞(P〈0.01)。结论:BAG2是由蛋白酶体抑制作用诱导产生的新型分子,在蛋白酶体抑制剂诱导的甲状腺癌细胞的死亡中起着促凋亡作用。 展开更多
关键词 bcl-2相关抗凋亡基因2 蛋白酶体抑制剂 凋亡 甲状腺肿瘤 bcl-2-associated athanogene 2
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Functional Characterization of the Group Ⅰ Alphabaculovirus Specific Gene ac73 被引量:1
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作者 Wei Shao Lihong He +5 位作者 Qingxiu Chen Jiang Li Fei Deng Hualin Wang Zhihong Hu Manli Wang 《Virologica Sinica》 SCIE CAS CSCD 2019年第6期701-711,共11页
Baculoviridae is a family of large DNA viruses that specifically infect insects. It contains four genera, Alpha-, Beta-,Gamma-, and Deltabaculovirus. Alphabaculovirus is further divided into Group Ⅰ and Ⅱ, and Group... Baculoviridae is a family of large DNA viruses that specifically infect insects. It contains four genera, Alpha-, Beta-,Gamma-, and Deltabaculovirus. Alphabaculovirus is further divided into Group Ⅰ and Ⅱ, and Group Ⅰ appears to be emerged most recently among all baculoviruses. Interestingly, there are 12 Group Ⅰ specific genes that are only found in this lineage. Studying these genes is helpful to understand how baculoviruses evolved. Here, we reported the functional analyzing results of ac73, a function unknown Group Ⅰ specific gene of Autographa californica multiple nucleopolyhedrovirus(Ac MNPV) which is the type species of baculovirus. The AC73 protein encoded by ac73 was found to be expressed during the late stage of infection and incorporated into the nucleocapsids of budded virus(BV) and occlusionderived virus(ODV). In infected cells, AC73 resided mainly in the ring zone region of the nucleus, and appeared to be assembled into occlusion bodies(OBs). The ac73 knockout and repaired viruses were constructed and studied by in vitro and in vivo infection. Although ac73 was not essential for BV and ODV or OB formation, the BV titer and viral infectivity in insect larvae of ac73 knockout Ac MNPV decreased by about 5–8 and 3–4 fold compared to those of wild type virus,respectively, suggesting ac73 contributed to infectious BV production and viral infectivity in vivo. This research provides new insight into the function of this Group I specific gene. 展开更多
关键词 BACULOVIRUS AC73 Group NUCLEOCAPSID bcl-2-associated athanogene(BAG) domain
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