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ERK phosphorylation functions in invadopodia formation in tongue cancer cells in a novel silicate fibre-based 3D cell culture system 被引量:2
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作者 Masaharu Noi Ken-Ichi Mukaisho +8 位作者 Saori Yoshida Shoko Murakami Shinya Koshinuma Takeshi Adachi Yoshisato Machida Masashi Yamori Takahisa Nakayama Gaku Yamamoto Hiroyuki Sugihara 《International Journal of Oral Science》 SCIE CAS CSCD 2018年第4期253-262,共10页
To screen for additional treatment targets against tongue cancer, we evaluated the contributions of extracellular signal-related kinase(ERK), AKT and ezrin in cancer development. Immunohistochemical staining showed th... To screen for additional treatment targets against tongue cancer, we evaluated the contributions of extracellular signal-related kinase(ERK), AKT and ezrin in cancer development. Immunohistochemical staining showed that ERK and ezrin expressions were significantly higher in invasive squamous cell carcinoma than in carcinoma in situ. To investigate the roles of ERK and ezrin in cancer development, we used the non-woven silica fibre sheet Cellbedwith a structure resembling the loose connective tissue morphology in a novel 3 D culture system. We confirmed that the 3 D system using CellbedTMaccurately mimicked cancer cell morphology in vivo. Furthermore, cell projections were much more apparent in 3 D-cultured tongue cancer cell lines than in 2 D cultures. Typically, under conventional 2 D culture conditions, F-actin and cortactin are colocalized in the form of puncta within cells.However, in the 3 D-cultured cells, colocalization was mainly observed at the cell margins, including the projections. Projections containing F-actin and cortactin colocalization were predicted to be invadopodia. Although suppressing ezrin expression with small interfering RNA transfection caused no marked changes in morphology, cell projection formation was decreased, and the tumour thickness in vertical sections after 3 D culture was markedly decreased after suppressing ERK activity because both the invasion ability and proliferation were inhibited. An association between cortactin activation as well as ERK activity and invadopodia formation was detected. Our novel 3 D culture systems using Cellbed? are simple and useful for in vitro studies before conducting animal experiments. ERK contributes to tongue cancer development by increasing both cancer cell proliferation and migration via cortactin activation. 展开更多
关键词 ERK phosphorylation functions in invadopodia formation in tongue cancer cells in a novel silicate fibre-based 3D cell culture sy HSC
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3D/4D printed versatile fibre-based wearables for embroidery, AIE-chemosensing, and unidirectional draining 被引量:1
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作者 Pengchao Liu Chengshengze Chu +10 位作者 Wenqi Qiu Lizi Cheng Jialun Gu Zhengyi Mao Zheng Zhao Xinyuan He Guo Liu Chen Peng Kwan Man Ben Zhong Tang Jian Lu 《Aggregate》 EI CAS 2024年第3期374-383,共10页
Fibre-based wearables for embroidery,chemosensing,and biofluid’s unidirectional draining with goodflexibility,tunability,and designability drive technological advance.However,synthetic polymerfibres are non-degradabl... Fibre-based wearables for embroidery,chemosensing,and biofluid’s unidirectional draining with goodflexibility,tunability,and designability drive technological advance.However,synthetic polymerfibres are non-degradable,threatening the environment and human health.Herein,we have developed versatile microfibre-based wearables by combining many advantages in one platform of biodegradable polylactic acid(PLA)and melt electrowriting strategy.Diverse potential applications of PLA wearables are achieved byflexibly designing their printingfiles,components and structures.Three-dimensional printingfiles are generated from two-dimensional images to fabricate‘embroidery-like’patterns.PLA/aggregation-induced emissionfluorogens(AIE)chemosensors exhibit colorimetric andfluorescent colour changes upon exposure to amine vapours.Janus PLA-cotton textiles with a hydropho-bic/hydrophilic structure could facilitate unidirectional draining of sweats which is favourable for the management of temperature and humidity on the surface of skin.The proposed platform can not only broaden the design possibilities in 3D/4D printing but also offer wide potential applications for functional wearables. 展开更多
关键词 3D/4D printing aggregation-induced emission CHEMOSENSING fibre-based wearable polylactic acid unidirectional draining
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Hybrid multimode - multicore fibre based holographic endoscope for deep-tissue neurophotonics 被引量:3
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作者 Yang Du Sergey Turtaev +4 位作者 Ivo T Leite Adrian Lorenz Jens Kobelke Katrin Wondraczek Tomas Cizmar 《Light(Advanced Manufacturing)》 2022年第3期84-92,共9页
In-vivo microendoscopy in animal models became a groundbreaking technique in neuroscience that rapidly expands our understanding of the brain.Emerging hair-thin endoscopes based on multimode fibres are now opening up ... In-vivo microendoscopy in animal models became a groundbreaking technique in neuroscience that rapidly expands our understanding of the brain.Emerging hair-thin endoscopes based on multimode fibres are now opening up the prospect of ultra-minimally invasive neuroimaging of deeply located brain structures.Complementing these advancements with methods of functional imaging and optogenetics,as well as extending its applicability to awake and motile animals constitute the most pressing challenges for this technology.Here we demonstrate a novel fibre design capable of both,high-resolution imaging in immobilised animals and bending-resilient optical addressing of neurons in motile animals.The optimised refractive index profile and the probe structure allowed reaching a spatial resolution of 2μm across a 230μm field of view for the initial layout of the fibre.Simultaneously,the fibre exhibits negligible cross-talk between individual inner-cores during fibre deformation.This work provides a technological solution for imaging-assisted spatially selective photo-activation and activity monitoring in awake and freely moving animal models. 展开更多
关键词 Multimode fibre Multicore fibre fibre-based imaging MICROENDOSCOPY ENDOMICROSCOPY Holographic endoscopy
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