TNFα-Induced Expression of Transport Protein Genes in HUVEC Cells Is Associated with Enhanced Expression of Transcription Factor Genes RELB and NFKB2 of the Non-Canonical NF-κB Pathway


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Endothelial HUVEC cells used as an in vitro model of the endothelial monolayer in placental barrier were activated by TNFα in a dose of 2 ng/ml for 24 h. Significant changes in the expression of genes of the SLC family transport protein were observed: an increase in the expression of SLC7A2, SLC12A2, SLC9B2, SLC25A37, SLC16A9, and SLC41A2 and a decrease in the expression of SLC40A1. These transporters participate in the transport of iron, magnesium, sodium, potassium, and chloride ions, protons, and amino acids. It was also found that SLC7A2, SLC12A2, SLC9B2, SLC25A37, and SLC41A2 genes have binding sites for transcriptional factor RelB that together with NFKB2 is the main effector of the non-canonical NF-κB pathway. The expression of RELB and NFKB2 genes was also significantly enhanced in TNFα-activated HUVEC cells, which can attest to the important role of the non-canonical NF-κB pathway in the regulation of gene expression of transport proteins in response to TNFα stimulation.

About the authors

E. N. Knyazev

BioClinilum Research Center

Author for correspondence.
Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow

D. V. Mal’tseva

BioClinilum Research Center

Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow

A. A. Zacharyants

BioClinilum Research Center

Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow

G. S. Zakharova

BioClinilum Research Center

Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow

O. V. Zhidkova

State Research Center Institute of Biomedical Problems, Russian Academy of Sciences

Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow

A. A. Poloznikov

BioClinilum Research Center

Email: e.knyazev@bioclinicum.com
Russian Federation, Moscow


Copyright (c) 2018 Springer Science+Business Media, LLC, part of Springer Nature

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies