Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10495/8362
Título : Phenotype analysis of dermal-epidermal organotypics made with hacat cell line seeding on top of three human fibroblast populated matrices (polyethylene terephthalate, fibrin or collagen I+III)
Autor : Pérez Cardona, David José
Restrepo Múnera, Luz Marina
metadata.dc.subject.*: Fibroblastos
Fibrina
Colágeno
Tereftalatos polietilenos
Queratinocitos
Céelulas HaCaT
Ingeniería tisular
Medicina regenerativa
Fecha de publicación : 2017
Editorial : Facultad de Medicina. Corporación de Ciencias Básicas Biomédicas
Citación : Pérez Cardona D. Phenotype analysis of dermal-epidermal organotypics made with hacat cell line seeding on top of three human fibroblast populated matrices (polyethylene terephthalate, fibrin or collagen I+III) [tesis maestria]. Medellín: Universidad de Antioquia; 2017.
Resumen : ABSTARCT: The aim of this study was to phenotype determination of dermal-epidermal organotypics (DEpOs) made with a hypotetraploid human keratinocyte cell line known as HaCaT. Three matrices were used, polyethylene terephthalate, human fıbrin or type I and type III rat collagen mixture. Methods: Population doubling time and the mitogenic effect of several media were assessed by formazan production assay. Microanatomical features were evaluated by bright-field/phase-contrast microscopy and hematoxylin and eosin (H&E) staining. Keratinization development markers (i.e. Ki67, K14, K10, filaggrin and loricrin) were determined by indirect immunohistochemistry. Free fatty acids (FFAs) fraction was estimated by gas chromatography with fire ionization detector (GC-FID). Barrier function was estimated by transepithelial electrical resistance (TEER) as well as permeability to Lucifer yellow (LY) measuring. DNA content of HaCaT was determined by propidium iodide (PI) staining and flow cytometry. Findings: Used HaCaT need 16.92±2.03 hours to divide in used medium. Irrespective to matrix type, histology and immunohistochemistry DEpOs showed a poor stratified epidermis (3-5 layers). Flattened cell shape in all layers, no enucleation and a poor spatiotemporal expression of differentiation markers was obtained. All observed features were in accordance with parakeratotic keratinization. Poor FFA detected profile and low TEER values showed absence of a significantly barrier function which correlates with parakeratosis and results of permeability assay. HaCaT DNA content analysis by flow cytometry revealed the presence of at least two different populations. High genetic alterations events might provoke a decreased sensitivity of this cell line to differentiation factors (e.g. air-liquid raising, insulin, adenine, etc.), as was reported previously
Aparece en las colecciones: Instituto de Investigaciones Médicas

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