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. 2017 Aug 23;313(5):R560–R571. doi: 10.1152/ajpregu.00529.2016

Table 3.

Fold changes in mRNA of chemokines and adhesion molecules in mouse aortic endothelial cells

Veh
ABH
Vector
A1-sgRNA
CTRL HG + PA CTRL HG + PA ABH + l-NAME CTRL HG + PA CTRL HG + PA A1-sgRNA + l-NAME
MCP-1 1.03 ± 0.05 4.96 ± 0.54* 0.97 ± 0.03 1.87 ± 0.23*# 3.03 ± 0.39* 1.02 ± 0.08 5.04 ± 0.56* 0.63 ± 0.21 1.89 ± 0.26*# 3.13 ± 0.48*
ICAM-1 1.03 ± 0.08 5.00 ± 0.58* 1.05 ± 0.13 1.26 ± 0.21 3.48 ± 0.46* 1.04 ± 0.20 4.18 ± 0.66* 1.00 ± 0.11 1.40 ± 0.19 3.01 ± 0.51*
VCAM-1 1.07 ± 0.11 11.74 ± 2.71* 1.18 ± 0.13 1.90 ± 0.47 10.95 ± 2.03* 1.05 ± 0.15 12.14 ± 2.57* 1.13 ± 0.14 1.94 ± 0.42 9.66 ± 2.02*

Values are means ± SE; n = 5 experiments. mRNA levels of MCP-1, ICAM-1, and V-CAM-1 in mouse aortic endothelial cells (MAECs) with and without arginase inhibitor (ABH), nitric oxide synthase inhibitor [nitro-l-arginine methyl ester (l-NAME)] treatment, or A1 downregulation by CRISPR/Cas 9-transduction of sgRNA after a 48-h incubation in normal media (CTRL) or media containing high glucose and palmitate (HG + PA).

*

P < 0.05 vs. CTRL vehicle or vector-transfected groups.

#

P < 0.05 HG + PA + ABH or A1-sgRNA HG + PA vs. Veh HG + PA or vector-transfected HG + PA groups, respectively.