Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Oberbauer, E; Steffenhagen, C; Feichtinger, G; Hildner, F; Hacobian, A; Danzer, M; Gabriel, C; Redl, H; Wolbank, S.
A Luciferase-Based Quick Potency Assay to Predict Chondrogenic Differentiation.
Tissue Eng Part C Methods. 2016; 22(5):487-495 Doi: 10.1089/ten.TEC.2015.0435 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
GABRIEL Christian
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Chondrogenic differentiation of adipose-derived stem cells (ASC) is challenging but highly promising for cartilage repair. Large donor variability of chondrogenic differentiation potential raises the risk for transplantation of cells with reduced efficacy and a low chondrogenic potential. Therefore, quick potency assays are required to control the potency of the isolated cells before cell transplantation. Current in vitro methods to analyze the differentiation capacity are time-consuming, and thus, a novel enhancer and tissue-specific promoter combination was used for the detection of chondrogenic differentiation of ASC in a novel quick potency bioassay. Human primary ASC were cotransfected with the Metridia luciferase-based collagen type II reporter gene pCMVE_ACDCII-MetLuc together with a Renilla control plasmid and analyzed for their chondrogenic potential. On day 3 after chondrogenic induction, the luciferase activity was induced in all tested donors under three-dimensional culture conditions and, in a second approach, also under two-dimensional (2D) culture conditions. With our newly developed quick potency bioassay, we can determine chondrogenic potential already after 3 days of chondrogenic induction and under 2D culture conditions. This will enhance the efficiency of testing cell functionality, which should allow in the future to predict the suitability of cells derived from individual patients for cell therapies in a very short time and at low costs.
Find related publications in this database (using NLM MeSH Indexing)
Adipose Tissue - cytology
Adipose Tissue - metabolism
Biological Assay - methods
Cell Differentiation -
Cells, Cultured -
Chondrocytes - cytology
Chondrocytes - metabolism
Chondrogenesis - physiology
Collagen Type II - genetics
Collagen Type II - metabolism
Humans -
Luciferases - genetics
Luciferases - metabolism
Polymerase Chain Reaction - methods
SOX9 Transcription Factor - genetics
SOX9 Transcription Factor - metabolism
Tissue Engineering - methods

© Med Uni Graz Impressum