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Physiological effects of amyloid precursor protein and its derivatives on neural stem cell biology and signaling pathways involved 被引量:3
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作者 Raquel Coronel Charlotte Palmer +4 位作者 Adela Bernabeu-Zornoza María Monteagudo Andreea Rosca Alberto Zambrano Isabel Liste 《Neural Regeneration Research》 SCIE CAS CSCD 2019年第10期1661-1671,共11页
The pathological implication of amyloid precursor protein(APP)in Alzheimer’s disease has been widely documented due to its involvement in the generation of amyloid-β peptide.However,the physiological functions of AP... The pathological implication of amyloid precursor protein(APP)in Alzheimer’s disease has been widely documented due to its involvement in the generation of amyloid-β peptide.However,the physiological functions of APP are still poorly understood.APP is considered a multimodal protein due to its role in a wide variety of processes,both in the embryo and in the adult brain.Specifically,APP seems to play a key role in the proliferation,differentiation and maturation of neural stem cells.In addition,APP can be processed through two canonical processing pathways,generating different functionally active fragments:soluble APP-α,soluble APP-β,amyloid-β peptide and the APP intracellular C-terminal domain.These fragments also appear to modulate various functions in neural stem cells,including the processes of proliferation,neurogenesis,gliogenesis or cell death.However,the molecular mechanisms involved in these effects are still unclear.In this review,we summarize the physiological functions of APP and its main proteolytic derivatives in neural stem cells,as well as the possible signaling pathways that could be implicated in these effects.The knowledge of these functions and signaling pathways involved in the onset or during the development of Alzheimer’s disease is essential to advance the understanding of the pathogenesis of Alzheimer’s disease,and in the search for potential therapeutic targets. 展开更多
关键词 AMYLOID precursor protein APP SOLUBLE APP alpha SOLUBLE APP beta AMYLOID beta peptide APP intracellular domain NEURAL stem CELLS NEURAL progenitor CELLS neurogenesis signaling pathways
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Wnt信号通路对vaspin诱导大鼠骨髓间充质干细胞成骨分化的影响 被引量:5
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作者 陈坤 高飞 《中国临床研究》 CAS 2015年第11期1415-1417,1421,共4页
目的研究Wnt/胞内β-连锁蛋白(β-catenin)信号通路对脂肪组织特异性丝氨酸蛋白酶抑制剂(vaspin)介导大鼠骨髓间充质干细胞(BMSCs)成骨分化的影响。方法体外培养4周龄雄性SD大鼠的BMSCs,分为4组:对照组,实验1、2、3组,分别加入成骨诱导... 目的研究Wnt/胞内β-连锁蛋白(β-catenin)信号通路对脂肪组织特异性丝氨酸蛋白酶抑制剂(vaspin)介导大鼠骨髓间充质干细胞(BMSCs)成骨分化的影响。方法体外培养4周龄雄性SD大鼠的BMSCs,分为4组:对照组,实验1、2、3组,分别加入成骨诱导液、含50 ng/ml、100 ng/ml vaspin的成骨诱导液及含100 ng/ml vaspin成骨诱导液+Dickkopf1(DKK1,Wnt/β-catenin信号通路特异性阻断剂),于成骨诱导第7天酶标仪检测碱性磷酸酶(ALP)活性,逆转录-聚合酶链反应(RT-PCR)检测成骨分化相关基因:ALP、核心蛋白结合因子2(RUNX2)、成骨细胞特异性转录因子Osterix(OSX)mRNA及β-catenin的表达水平。结果体外培养BMSCs,并加入不同浓度vaspin诱导后,实验1、2组ALP活性较对照组增加,并呈vaspin浓度依赖性(P均<0.05);成骨分化基因ALP、RUNX2、OSX mRNA表达水平增加,亦呈vaspin浓度依赖性(P均<0.05);β-catenin表达水平仅在加入100 ng/ml vaspin时升高(P<0.05);加入DKK1后(实验3组),ALP活性及成骨分化各基因表达水平较实验2组(100 ng/ml vaspin)显著下降(P均<0.05),β-catenin表达水平也显著下降(P<0.05)。结论 Vaspin可通过Wnt/β-catenin通路促进大鼠BMSCs成骨分化。 展开更多
关键词 骨髓间充质干细胞 成骨分化 脂肪组织特异性丝氨酸蛋白酶抑制剂 Wnt/胞内β-连锁蛋白通路 核心蛋白结合因子2 成骨细胞特异性转录因子Osterix
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