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Eq upregulates protein expression of adhesion molecules in HUVECs.

By Fumitake Ito (6278396), Taisuke Mori (4017932), Yosuke Tarumi (6278399), Hiroyuki Okimura (6278402), Hisashi Kataoka (6278405), Yukiko Tanaka (3049038), Akemi Koshiba (6278408) and Jo Kitawaki (417818)

Abstract

<p>HUVECs were treated with various estrogens as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0211462#pone.0211462.g001" target="_blank">Fig 1</a>. (<b>A</b>) E-selectin, (<b>B</b>) ICAM-1, (<b>C</b>) P-selectin, and (<b>D</b>) VCAM-1 protein levels were quantified by EIA. Data are expressed as the mean ± SEM of four experiments. *<i>P</i> < 0.05 vs. vehicle alone.</p

Topics: Biochemistry, Cell Biology, Genetics, Molecular Biology, Physiology, Immunology, Developmental Biology, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, intercellular adhesion molecule, equilin treatment, NF -κB activation, adhesion molecules E-selectin, adhesion molecules, protein expression levels, ER, atherosclerosi, equine estrogen increases monocyte-endothelial adhesion, E 2 treatment, estrogen-replacement therapy, polymerase chain reaction, HUVEC, Conjugated equine estrogen, NF -κB subunit p 65, U 937 monocytoid cells, E 2, NF -κB proteins, Equilin
Year: 2019
DOI identifier: 10.1371/journal.pone.0211462.g002
OAI identifier: oai:figshare.com:article/7652774
Provided by: FigShare
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