Cell viability and proliferation capability of long-term human dental pulp stem cell cultures
Autor: | Ingrid Garzón, Víctor Carriel, Ana Celeste Oliveira, Miguel Alaminos, Miguel Angel Martin-Piedra, Camilo Andrés Alfonso-Rodríguez, Giuseppe Scionti |
---|---|
Přispěvatelé: | Universitat Politècnica de Catalunya. Departament de Ciència dels Materials i Enginyeria Metal·lúrgica |
Rok vydání: | 2014 |
Předmět: |
Cell viability
Cancer Research Time Factors Cell Survival Immunology Population Cell Culture Techniques Tetrazolium Salts Apoptosis electron-probe x-ray microanalysis Biology Enginyeria dels materials [Àrees temàtiques de la UPC] In Situ Nick-End Labeling Humans Immunology and Allergy Tissue engineering Viability assay education Cells Cultured Dental Pulp Genetics (clinical) Cell Proliferation Transplantation education.field_of_study TUNEL assay Cell growth Microfilament Proteins Mesenchymal stem cell Trypan Blue Cell Biology Caspases Initiator Neoplasm Proteins Cell biology Adult Stem Cells Enginyeria de teixits Oncology Cell culture dental pulp Stem cell Apoptosis Regulatory Proteins mesenchymal stromal cells |
Zdroj: | Recercat. Dipósit de la Recerca de Catalunya instname UPCommons. Portal del coneixement obert de la UPC Universitat Politècnica de Catalunya (UPC) |
ISSN: | 1465-3249 |
DOI: | 10.1016/j.jcyt.2013.10.016 |
Popis: | ackground aims Evaluation of cell viability is one of the most important steps of the quality control process for therapeutic use of cells. The aim of this study was to evaluate the long-term cell viability profile of human dental pulp stem cell (hDPSC) subcultures (beyond 10 passages) to determine which of these passages are suitable for clinical use and to identify the cell death processes that may occur in the last passages. Methods Four different cell viability assays were combined to determine the average cell viability levels at each cell passage: trypan blue exclusion test, water-soluble tetrazolium 1 (WST-1), LIVE/DEAD Viability/Cytotoxicity Kit and electron probe x-ray microanalysis (EPXMA). Apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay and caspase 4 and BCL7C Western blotting, and cell proliferation was analyzed by WST-1 and proliferating cell nuclear antigen protein detection. Results hDPSCs showed high average cell viability levels from passages 11–14, with adequate cytoplasmic and mitochondrial functionality at these subcultures. A non-significant trend to decreased cell proliferation was found from passages 16–20. EPXMA and TUNEL analyses suggested that a pre-apoptotic process could be activated from passages 15–20 (P < 0.001), with a correlation with caspase 4 and BCL7C expression. Conclusions hDPSCs corresponding to passages 11–14 show adequate cell function, proliferation and viability. These cells could be considered as potentially useful for clinical applications. |
Databáze: | OpenAIRE |
Externí odkaz: |