Aquaporin 1 and 5 expression decreases during human intervertebral disc degeneration: novel HIF-1-mediated regulation of aquaporins in NP cells.

JOHNSON, Zariel I, GOGATE, Shilpa S, DAY, Rebecca, BINCH, Abbie, MARKOVA, Dessislava Z, CHIVERTON, Neil, COLE, Ashley, CONNER, Matthew, SHAPIRO, Irving M, LE MAITRE, Christine and RISBUD, Makarand V (2015). Aquaporin 1 and 5 expression decreases during human intervertebral disc degeneration: novel HIF-1-mediated regulation of aquaporins in NP cells. Oncotarget, 6 (14), 11945-11958.

[img]
Preview
PDF
Conner_Le_Maitre_Aquaporin_1_and_5_expression.pdf - Published Version
Creative Commons Attribution Non-commercial No Derivatives.

Download (2MB) | Preview

Abstract

Objectives of this study were to investigate whether AQP1 and AQP5 expression is altered during intervertebral disc degeneration and if hypoxia and HIF-1 regulate their expression in NP cells. AQP expression was measured in human tissues from different degenerative grades; regulation by hypoxia and HIF-1 was studied using promoter analysis and gain- and loss-of-function experiments. We show that both AQPs are expressed in the disc and that mRNA and protein levels decline with human disease severity. Bioinformatic analyses of AQP promoters showed multiple evolutionarily conserved HREs. Surprisingly, hypoxia failed to induce promoter activity or expression of either AQP. While genomic chromatin immunoprecipitation showed limited binding of HIF-1α to conserved HREs, their mutation did not suppress promoter activities. Stable HIF-1α suppression significantly decreased mRNA and protein levels of both AQPs, but HIF-1α failed to induce AQP levels following accumulation. Together, our results demonstrate that AQP1 and AQP5 expression is sensitive to human disc degeneration and that HIF-1α uniquely maintains basal expression of both AQPs in NP cells, independent of oxemic tension and HIF-1 binding to promoter HREs. Diminished HIF-1 activity during degeneration may suppress AQP levels in NP cells, compromising their ability to respond to extracellular osmolarity changes.

Item Type: Article
Research Institute, Centre or Group - Does NOT include content added after October 2018: Biomedical Research Centre
Identification Number: https://doi.org/10.18632/oncotarget.3631
Page Range: 11945-11958
Depositing User: Users 3084 not found.
Date Deposited: 27 May 2015 13:12
Last Modified: 18 Mar 2021 04:47
URI: https://shura.shu.ac.uk/id/eprint/9872

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics