首页> 外文会议>2015 Joint Conference of the IEEE International Frequency Control Symposium amp; European Frequency and Time Forum >Monitoring the adhesion process of tendon stem cells using shear-horizontal surface acoustic wave sensors
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Monitoring the adhesion process of tendon stem cells using shear-horizontal surface acoustic wave sensors

机译:使用剪切水平表面声波传感器监测肌腱干细胞的粘附过程

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Cell adhesion to a substrate or extracellular matrix (ECM) plays an important role in a variety of cellular functions, such as cell migration, proliferation, differentiation, and tissue formation. Shear-horizontal surface acoustic wave (SH-SAW) sensors can detect cell behaviors in liquid in a non-invasive, simple and quantitative manner. As the key part of SH-SAW, acoustic-wave guiding layer plays a crucial role in improving sensor performance. Parylene-C (poly(2-chloro-p-xylylene)) has been proven as ideal guiding layer due to its good uniformity, compactness and adhesion to substrate. Of comparable cell and protein compatibility to the tissue culture substrate, parylene-C films also have preferable effects as the bio-sensitive interface on SH-SAW sensors. In this study, SH-SAW sensor with parylene-C acoustic-wave guiding layer was adopted to monitor the adhesion process of tendon stem cells (TSCs), a newly discovered stem cell type in tendons. TSC suspensions of different concentrations (0.5×10, 1.0×10, 2.0×10, 4.0×10 cell/ml) were added to collagen-coated PDMS wells successively. The cells were maintained in the incubator for 10 hr, during which corresponding S spectrums were recorded every 1 min. The results indicated that there was a sharp increase in S loss in the beginning of incubation. With incubation continued, the increase rate reduced gradually, and S loss tended to be stable. S phase decreased continuously at first, and then entered a plateau with continued incubation. These changes are considered to be related to the integrin-ECM protein interactions and focal adhesion formation occurring in TSC adhesion process. In addition, as TSC suspension concentration increased, the final value of S loss change due to TSC adhesion was increased. SH-SAW sensors exhibit high sensitivity and stability in TSC adhesion monit- ring, indicating their potential for investigating cell biology in general and cell adhesion in particular.
机译:细胞对基质或细胞外基质(ECM)的粘附在多种细胞功能(例如细胞迁移,增殖,分化和组织形成)中起着重要作用。剪切水平表面声波(SH-SAW)传感器可以以非侵入性,简单且定量的方式检测液体中的细胞行为。作为SH-SAW的关键部分,声波引导层在提高传感器性能方面起着至关重要的作用。聚对二甲苯-C(聚(2-氯-对-亚二甲苯基))由于其良好的均匀性,致密性和对基材的粘附性,已被证明是理想的引导层。具有与组织培养基质相当的细胞和蛋白质相容性,聚对二甲苯-C膜作为SH-SAW传感器上的生物敏感界面也具有较好的效果。在这项研究中,采用带有聚对二甲苯-C声波引导层的SH-SAW传感器来监测肌腱干细胞(TSC)的粘附过程,这是一种新发现的肌腱干细胞类型。将不同浓度(0.5×10、1.0×10、2.0×10、4.0×10细胞/ ml)的TSC悬浮液依次添加到胶原包被的PDMS孔中。将细胞在培养箱中保持10小时,其间每1分钟记录一次相应的S光谱。结果表明,在孵育开始时,S损失急剧增加。随着温育的继续,增加率逐渐降低,并且S损失趋于稳定。 S期首先连续降低,然后进入持续培养的平台期。这些变化被认为与TSC粘附过程中发生的整联蛋白-ECM蛋白相互作用和粘着斑形成有关。此外,随着TSC悬浮液浓度的增加,由于TSC粘附而导致的S损失变化的最终值会增加。 SH-SAW传感器在TSC粘附监测中表现出高灵敏度和稳定性,表明它们有潜力用于一般研究细胞生物学,尤其是研究细胞粘附。

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