Back to Search
Start Over
Evaluation of transporter expression in HK-2 cells after exposure to free and ester-bound 3-MCPD.
- Source :
-
Toxicology reports [Toxicol Rep] 2021 Feb 23; Vol. 8, pp. 436-442. Date of Electronic Publication: 2021 Feb 23 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- 3-Monochloropropane-1,2-diol (3-MCPD) is a food processing contaminant in some infant formula products and other foods in the United States. Although rodent studies have demonstrated that 3-MCPD and its palmitic esters have the potential to induce nephrotoxicity, our recent human cell culture studies using the human renal proximal tubule cell line HK-2 have not strongly supported this finding. Considering this disparity, we sought to examine whether changes in transporter gene expression on proximal tubule cells could be modulated by these compounds and allow us to glean mechanistic information on a possible indirect path to proximal tubule injury in vivo . If fundamental processes like water and solute transport could be disrupted by 3-MCPD compounds, then a new avenue of toxicity could be further explored in both infant and adult models. In our current study, we used HK-2 cells as an in vitro cellular model of human proximal tubule cells to investigate the effects of low (10 μM) and high (100 μM) 3-MCPD compound exposures to these cells for 24 hours (h) on the expression of 20 transporter genes that are known to be relevant to proximal tubules. Although we detected consistent upregulation of AQP1 expression at the RNA transcript level following HK-2 treatment with both low and high doses of several ester-bound 3-MCPD compounds, these increases were not associated with statistically significant elevations in their protein expression levels. Moreover, we observed a lack of modulation of other members of the AQP protein family that are known to be expressed by human proximal tubule cells. Overall, our study suggests the possibility that 3-MCPD-related nephrotoxicity could be associated with indirect modes of action relating to aquaporin homeostasis, but additional studies with other human-derived models would be pertinent to further explore these findings and to better understand transporter expression differences under different stages of proximal tubule development.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (© 2021 Published by Elsevier B.V.)
Details
- Language :
- English
- ISSN :
- 2214-7500
- Volume :
- 8
- Database :
- MEDLINE
- Journal :
- Toxicology reports
- Publication Type :
- Academic Journal
- Accession number :
- 33717996
- Full Text :
- https://doi.org/10.1016/j.toxrep.2021.02.017