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抗血管生成致内皮细胞释放外泌体促进肿瘤血管形成 被引量:1
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作者 曾烨 bingmei mfu 《医用生物力学》 EI CAS CSCD 北大核心 2019年第A01期50-50,共1页
抗血管生成疗法(anti-angiogenic therapies,AATs)被用于多种恶性癌症的治疗,其临床疗效因继发性的肿瘤血管形成(vasculogenesis)和肿瘤生长而受限[1-3]。本研究试图揭示AATs治疗后肿瘤血管生成和肿瘤生长的分子机制。首先,将微小RNA-9(... 抗血管生成疗法(anti-angiogenic therapies,AATs)被用于多种恶性癌症的治疗,其临床疗效因继发性的肿瘤血管形成(vasculogenesis)和肿瘤生长而受限[1-3]。本研究试图揭示AATs治疗后肿瘤血管生成和肿瘤生长的分子机制。首先,将微小RNA-9(microRN A-9,miR-9)转染至人脐静脉内皮细胞,以模拟肝癌中的肿瘤相关性内皮细胞[4-5],探讨AATs对内皮细胞的影响及其作用机制。发现,抗血管生成抑制剂凡德他尼(vandetanib)完全抑制了miR-9诱导的血管生成,并促进了人脐静脉内皮细胞的自噬,同时,还诱导了富血管生成因子(vascular endothelial growth factor,VEGF)外泌体的释放。这些富VEGF外泌体可显著促进内皮血管生成和肝癌细胞血管生成拟态,促进肝癌在裸鼠体内的生长。抗自噬也可以抑制血管内皮细胞的血管生成,但是与AATs相似,自噬抑制剂3-MA促进了富VEGF外泌体的释放。体外实验表明,抑制外泌体的释放,或使用VEGF中和性抗体处理富VEGF外泌体,可以显著抑制肿瘤细胞的血管生成拟态。由此可见,AATs和抗自噬后的肿瘤血管形成和肿瘤生长是内皮细胞和肿瘤细胞相互作用的结果,由富VEGF的外泌体所介导。此外,内皮细胞miR-9表达水平受流体剪切力调控。力学因素在抗血管生成致内皮细胞释放外泌体促进肿瘤血管形成中的作用及机制有待深入探究。 展开更多
关键词 肿瘤血管形成 肿瘤生长 抗血管生成 外泌体 内皮细胞
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Mechano-Sensing by Endothelial Primary Cilium
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作者 Huan Yin Lizhen Wang +1 位作者 bingmei mfu Yubo Fan 《医用生物力学》 EI CAS CSCD 北大核心 2019年第A01期178-179,共2页
Introduction Primary cilium is a non-motile microstructure,protruding from cell surface of most mammalian cells.It was previously thought to be vestigial.However,recent studies indicate that it may serve as one of the... Introduction Primary cilium is a non-motile microstructure,protruding from cell surface of most mammalian cells.It was previously thought to be vestigial.However,recent studies indicate that it may serve as one of the most vital mechanosensors for many types of cells such as epithelial and endothelial cells and osteocytes.Protruding from the apical membrane,the primary cilium can directly sense subtle variation of mechanical forces exerted on the cell and then transduce the mechanical cues into biochemical signals into the cell,although the mechanism remain elusive.Vascular endothelial cells(ECs)lining the inner wall of our blood vessels are continuously exposed to the blood flow.In order to maintain proper functions for the cardiovascular system,ECs should have a variety of mechano-sensors and transducers to sense the blood flow change and adjust the vessel size and transport across the vessel wall accordingly.Among more than a dozen recognized EC mechano-sensors,the primary cilium has drawn more and more attention recently.Primary cilium on endothelial cells is essential for the homeostasis of vessels.It is reported to be prevalent in areas of disturbed flow where atherosclerosis and intracranial aneurysm usually occur.Deficiencies of primary cilia may promote atherosclerosis,endothelial-to-mesenchymal transition(EndoMT)and loss of direction orientation,to name a few.Therefore understanding why the primary cilia are necessary to maintain the homeostasis of blood vessels and how will help us develop better treatment strategies for the common cardiovascular diseases.Dimension and structure of primary cilium Primary cilium is reported to be shorter than 8 in length and about 0.2 in diameter.The length of primary cilium varies in different cell types and under different conditions.The major structural components of the primary cilium include basal body,ciliary axoneme(consisting of nine doublet microtubules),ciliary membrane,transition zone,basal feet,and striated rootlets.Each part of the primary cilium is essential and has specific function.Current methods investigating the EC primary cilium as a mechano-sensor:Immunostaining and imaging techniques have been used to investigate the molecular mechanisms by which EC primary cilium serves as a mechano-sensor and transducer.It has been found that various proteins locate on the primary cilium,working together to maintain the function of primary cilium.Some proteins function as ion-channels,mediating Ca2+entry into the primary cilium.Some are involved in the cascade signal pathway.Others are related to the assembly and maintenance of primary cilium.Briefly,the flow induces the deflection of the EC primary cilium,which triggers calcium increase via opening of the PC2 cation channel that is responsible for calcium ion influx.This PC2 cation channel is localized to the primary cilium and is assumed to be stretch-activated.The resulting change in the intracellular calcium concentration then regulates numerous molecular activities inside the cell that contribute to vessel homeostasis.In addition to triggering calcium release,another mechanism has also been found in blood-pressure maintenance in the vasculature,where the vessel diameter is regulated by endothelial primary cilia through adjusting nitric oxide production.So far,little is known about the mechanical mechanism behind this deflection-triggered o-pening of signaling pathways.For example,what is the flow induced bending behavior and force distribution? What is the threshold value of stretch/defection for activating a corresponding signaling pathway? These all remain to be answered.In combination of image data and experiments,several computational models have been established to answer these questions.However,the current models are not able to include the complex structure of primary cilium and the model predictions are limited.Future studies With the development of super high resolution optical microscopy,more detailed images for the structural(molecular)components of EC primary cilia will be revealed,especially when the ECs are alive and the forces are known.Combining these experimental observations with more sophisticated mathematical models will elucidate the mechano-sensing mechanism of EC primary cilia,as the force and stress distribution on cilium along with other mechanical properties are still beyond the capability of experimental approaches due to the scales of the quantities involved.By using numerical approaches,much more detailed dynamic information can be obtained. 展开更多
关键词 ENDOTHELIAL CELLS PRIMARY CILIUM MECHANOSENSOR
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