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A scaffoldless technique for self-generation of three-dimensional keratinospheroids on liquid crystal surfaces

机译:液晶表面上三维角质球体自成的脚腰技术

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We describe a new scaffold-free three-dimensional (3D) cell culture model using cholesteryl ester based lyotropic liquid crystal (LC) substrates. Keratinocytes were deposited randomly on the LC surface where they self-assembled into 3D microtissues or keratinospheroids. The cell density required to form spheroids was optimized. We investigated cell viability using dead/live cell assays. The adhesion characteristics of cells within the microtissues were determined using histological sectioning and immunofluorescence staining. Fourier transform infrared spectroscopy (FTIR) was used to characterize the biochemistry of the keratinospheroids. We found that both cells and microtissues could migrate on the LC surface. The viability study indicated approximately 80% viability of cells in the microtissues up to 20 days of culture. Strong intercellular adhesion was observed in the stratification of the multi-layered microspheroids using field emission-scanning electron microscopy (FE-SEM) and histochemical staining. The cytoskeleton and vinculins of the cells in the microtissues were expressed diffusely, but the microtissues were enriched with lipids and nucleic acids, which indicates close resemblance to the conditions in vivo. The basic 3D culture model based on LC may be used for cell and microtissue migration studies in response to cytochemical treatment.
机译:我们使用基于胆固醇酯的增压液晶(LC)基材来描述一种新的无支腿三维(3D)细胞培养模型。在LC表面上随机沉积角质形成细胞,在那里它们自组装成3D微局部或角蛋白运动体。优化形成球状体所需的细胞密度。我们使用死/活细胞测定研究了细胞活力。使用组织学切片和免疫荧光染色测定微小细胞内细胞的粘附特性。傅里叶变换红外光谱(FTIR)用于表征角质体的生物化学。我们发现两个细胞和微发布都可以在LC表面上迁移。可行性研究表明,在微小训练中的细胞中的至少80%的活力高达20天。使用场发射扫描电子显微镜(Fe-SEM)和组织化学染色在多层微球体的分层中观察到强细胞间粘附。微小细胞中细胞的细胞骨架和vinculins弥漫性,但富含脂质和核酸的微生物诱导,这表明与体内病症感到紧密相似。基于LC的基本3D培养模型可用于响应细胞化学治疗的细胞和微囊迁移研究。

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