| Literature DB >> 31403625 |
Stephan R Künzel1, Charlotte Schaeffer2, Karolina Sekeres2, Carola S Mehnert2, Stephanie M Schacht Wall2, Manja Newe2, Susanne Kämmerer2, Ali El-Armouche3.
Abstract
Primary adult fibroblasts have become an important tool to study fibrosis, fibroblast interactions and inflammation in all body tissues. Since primary fibroblasts cannot divide indefinitely due to myofibroblast differentiation or senescence induction, new cultures must be established regularly. However, there are several obstacles to overcome during the processes of developing a reliable isolation protocol and primary fibroblast isolation itself: the method's degree of difficulty (especially for beginners), the risk of bacterial contamination, the required time until primary fibroblasts can be used for experiments, and subsequent cell quality and viability. In this study, a fast, reliable and easy-to-learn protocol to isolate and culture primary adult fibroblasts from mouse heart, lung, liver and kidney combining enzymatic digestion and ultrasonic agitation is provided.Entities:
Mesh:
Year: 2019 PMID: 31403625 DOI: 10.3791/59858
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355