TY - JOUR
T1 - In vitro assessment of human endothelial cell permeability
T2 - Effects of inflammatory cytokines and dengue virus infection
AU - Dewi, Beti Ernawati
AU - Takasaki, Tomohiko
AU - Kurane, Ichiro
N1 - Funding Information:
We thank Dr. M. Ito, Dr. S. Tajima, and Ms. R. Nerome, Laboratory of Vector-Borne Viruses, Department of Virology 1, National Institute of Infectious Diseases, for their technical help. This study was supported by the grant-in-aid (No. 12877045) from Ministry of Education, Sciences, Sports and Culture, Japan and the grant for Research on Emerging and Re-Emerging Infectious Diseases from Ministry of Health, Labour and Welfare, Japan.
PY - 2004/11
Y1 - 2004/11
N2 - Electrical resistance across human umbilical vein endothelial cells (HUVECs) was measured using an electrical cell sensor system. The transendothelial electrical resistance (TEER) value was used to estimate the permeability through endothelial cells in vitro. Decrease in the TEER value was associated with increase in the passage of albumin through endothelial cells in the albumin permeability assay. The effects of cytokines and dengue virus infection on the permeability of HUVECs were examined by measuring the TEER value. Tumor necrosis factor alpha (TNF-α) at 1 and 0.1 μg/ml decreased the TEER value, but TNF-α at lower dose did not. Interferon-gamma (IFN-γ) at 1 μg/ml also decreased the TEER value. In contrast, interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10) or interferon-beta (IFN-β) did not decrease the TEER value. The decrease in the TEER value was associated with the morphological changes of HUVECs. Dengue virus infection at a multiplicities of infection (m.o.i.) of 5 pfu/cell decreased the TEER value. Infection at an m.o.i. of 0.5 pfu/cell did not decrease the TEER value; however, addition of 0.01 μg/ml of TNF-α to these infected endothelial cells decreased the TEER value. The results suggest that TNF-α and dengue virus infection decrease synergistically the TEER value of endothelial cells. The TEER method is easy, reliable and can be applicable to further analysis of the increase in the permeability of endothelial cells in vitro induced by inflammatory cytokines and dengue virus infection.
AB - Electrical resistance across human umbilical vein endothelial cells (HUVECs) was measured using an electrical cell sensor system. The transendothelial electrical resistance (TEER) value was used to estimate the permeability through endothelial cells in vitro. Decrease in the TEER value was associated with increase in the passage of albumin through endothelial cells in the albumin permeability assay. The effects of cytokines and dengue virus infection on the permeability of HUVECs were examined by measuring the TEER value. Tumor necrosis factor alpha (TNF-α) at 1 and 0.1 μg/ml decreased the TEER value, but TNF-α at lower dose did not. Interferon-gamma (IFN-γ) at 1 μg/ml also decreased the TEER value. In contrast, interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10) or interferon-beta (IFN-β) did not decrease the TEER value. The decrease in the TEER value was associated with the morphological changes of HUVECs. Dengue virus infection at a multiplicities of infection (m.o.i.) of 5 pfu/cell decreased the TEER value. Infection at an m.o.i. of 0.5 pfu/cell did not decrease the TEER value; however, addition of 0.01 μg/ml of TNF-α to these infected endothelial cells decreased the TEER value. The results suggest that TNF-α and dengue virus infection decrease synergistically the TEER value of endothelial cells. The TEER method is easy, reliable and can be applicable to further analysis of the increase in the permeability of endothelial cells in vitro induced by inflammatory cytokines and dengue virus infection.
KW - Cytokine
KW - Dengue virus
KW - Endothelial cells
KW - Permeability
UR - http://www.scopus.com/inward/record.url?scp=4644326693&partnerID=8YFLogxK
U2 - 10.1016/j.jviromet.2004.06.013
DO - 10.1016/j.jviromet.2004.06.013
M3 - Article
C2 - 15381354
AN - SCOPUS:4644326693
SN - 0166-0934
VL - 121
SP - 171
EP - 180
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 2
ER -