A scaffoldless technique for self-generation of three-dimensional keratinospheroids on liquid crystal surfaces
Autor: | Kok Tung Thong, Azzura Ismail, Morgan Denyer, Chin Fhong Soon, Mohd Khairul Ahmad, SC Cheong, Kian Sek Tee, P Vyomesh, YH Kong |
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Rok vydání: | 2016 |
Předmět: |
Keratinocytes
0301 basic medicine Histology Cell Survival Cell Cell Culture Techniques Fluorescent Antibody Technique 02 engineering and technology Cell Line law.invention 03 medical and health sciences In vivo law Spectroscopy Fourier Transform Infrared medicine Humans Viability assay Cytoskeleton Tissue Engineering Chemistry Spheroid General Medicine 021001 nanoscience & nanotechnology Liquid Crystals Cell biology Medical Laboratory Technology 030104 developmental biology medicine.anatomical_structure Lyotropic liquid crystal Cell culture Electron microscope 0210 nano-technology |
Zdroj: | Biotechnic & Histochemistry. 91:283-295 |
ISSN: | 1473-7760 1052-0295 |
DOI: | 10.3109/10520295.2016.1158865 |
Popis: | 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. |
Databáze: | OpenAIRE |
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