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TrkB-shiRNA质粒转染心脏微血管内皮细胞 被引量:1
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作者 陈斯韵 曹亮 +4 位作者 李震 沈晓涛 郑馨 梁永佳 蔡冬青 《中国组织工程研究与临床康复》 CAS CSCD 北大核心 2010年第20期3655-3659,共5页
背景:脑源性神经营养因子与其受体TrkB在心脏与骨骼肌内皮细胞存在表达,在心脏血管系统的发育中及骨骼肌缺血时能有效促进血管新生,但其促血管新生的细胞与分子机制尚不清楚。目的:应用针对脑源性神经营养因子受体TrkB的shiRNA质粒对心... 背景:脑源性神经营养因子与其受体TrkB在心脏与骨骼肌内皮细胞存在表达,在心脏血管系统的发育中及骨骼肌缺血时能有效促进血管新生,但其促血管新生的细胞与分子机制尚不清楚。目的:应用针对脑源性神经营养因子受体TrkB的shiRNA质粒对心脏微血管内皮细胞进行转染,观察TrkB 3种亚型的表达及心脏微血管内皮细胞的生长状况和形态,初步探讨脑源性神经营养因子-TrkB通路在心脏微血管内皮细胞中的调控作用。方法:使用TrkB-shiRNA质粒转染大鼠心脏微血管内皮细胞,应用荧光实时定量PCR检测TrkB的3个亚型,TrkB-FL、TrkB-T1及TrkB-T2 mRNA的表达,并观察经转染的心脏微血管内皮细胞的增殖情况。结果与结论:应用TrkB-shiRNA质粒转染心脏微血管内皮细胞后,TrkB 3种亚型在转染后的4d内mRNA表达均下降(P<0.05或P<0.01),且经转染的心脏微血管内皮细胞的生长变慢。说明TrkB-shiRNA质粒可沉默心脏微血管内皮细胞的TrkB-FL、TrkB-T1及TrkB-T2的表达,且TrkB表达被抑制可能会影响心脏微血管内皮细胞的增殖。 展开更多
关键词 心脏微血管内皮细胞 脑源性神经营养因子 TRKB shiRNA trkb-fl TrkB-T1 TrkB-T2 细胞增殖
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The role of the TrkB-T1 receptor in the neurotrophin-4/5 antagonism of brain-derived neurotrophic factor on corticostriatal synaptic transmission 被引量:2
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作者 Elizabeth Hernandez-Echeagaray 《Neural Regeneration Research》 SCIE CAS CSCD 2020年第11期1973-1976,共4页
This manuscript reviews the function and fundamental characteristics of the neurotrophins and their receptors to introduce the reader to the differential effects exhibited by the neurotrophins;brain-derived neurotroph... This manuscript reviews the function and fundamental characteristics of the neurotrophins and their receptors to introduce the reader to the differential effects exhibited by the neurotrophins;brain-derived neurotrophic factor and neurotrophin 4/5 when acted together after sequential presentation.The neurotrophin 4/5 exhibits an inhibitory action on the modulatory effect of brain-derived neurotrophic factor in corticostriatal synapses when they are administered sequentially(brain-derived neurotrophic factor to neurotrophin 4/5).This inhibitory effect has not been previously documented and is relevant for these neurotrophins as both of them stimulate the TrkB receptor.The additive effect of these neurotrophins is also discussed and occurs when neurotrophin 4/5 exposure is followed by brain-derived neurotrophic factor in a mouse model of striatal degeneration.Occlusive and additive effects of both neurotrophins are accompanied by changes in the expression of the TrkB receptor isoforms,specifically TrkB-T1 and TrkB-FL,as well as differences in phosphorylation levels of the TrkB receptor.The results of the experiments described raise several questions to inquire about the role that TrkB-T1 receptor plays in striatal physiology,as well as the functional relevance of the interaction of brain-derived neurotrophic factor and neurotrophin 4/5 in the brain and more specifically at the striatal circuits in normal as well as pathological conditions. 展开更多
关键词 BRAIN-DERIVED NEUROTROPHIC factor NEUROTROPHIN 4/5 occlusive striatum synergic trkb-fl TrkB-T1
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