Isolation and Culture of Primary Brain Pericytes: A Procedure to Isolate and Culture Pericytes from Bovine Brain Capillaries Without Endothelial Cell Contamination
In this video, we demonstrate the procedure to isolate and culture pericytes from bovine brain capillaries without endothelial cell contamination.
Protocol
All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board. 1. Seeding and Culturing of Bovine Capillaries Day 0: Mix 0.7 mL of collagen IV stock with 6.3 mL of PBS. Add the solution to a T75-flask and leave the flask for 2 h at room temperature (RT) or leave it overnight at 4 °C. Remove the collagen solution from the flask and wash three times …
Representative Results
Figure 1: Culturing of capillaries and isolation of pericytes. Capillaries have been isolated from fresh bovine brain and seeded in culture flasks on day 0. Outgrowth from the bovine brain capillaries and the following isolation of pericytes were followed over days with a light microscope. Day 4a shows the endothelial cell growth prior to treatment with trypsin to remove endothelial cells an…
Disclosures
The authors have nothing to disclose.
Materials
PBS
Sigma Aldrich
D8537
Phosphate-buffered saline
Collagen IV
Sigma Aldrich
C5533
T-75 flask
Sigma Aldrich
CLS3972
Fetal bovine serum (FBS)
PAA/GE Healthcare
A15-101
Fibronectin
Sigma Aldrich
F1141
Trypsin-EDTA
Sigma Aldrich
T4299
Light microscope
Olympus
Olympus CK2
Upright light microscope with phase contrast
DMSO
Sigma Aldrich
471267
Heparin
Sigma Aldrich
H3149
Cell incubator
Thermo Fisher
Centrifuge
Thermo Fisher
Heraeus Multifuge 3SR+
Standard large volume centrifuge for spinning down cells
Isolation and Culture of Primary Brain Pericytes: A Procedure to Isolate and Culture Pericytes from Bovine Brain Capillaries Without Endothelial Cell Contamination. J. Vis. Exp. (Pending Publication), e20681, doi: (2023).