4.7 Article

Lactate released from human fibroblasts enhances Ni elution from Ni plate

Journal

TOXICOLOGY
Volume 453, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.tox.2021.152723

Keywords

Lactate; Nickel; HIF-1 alpha; Glycolysis; Fibroblast; Monocarboxylate transporter

Funding

  1. Cooperative Research Project Program of Joint Us-age/Research Center at the Institute of Development, Aging and Cancer, Tohoku University

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This study investigated the molecular mechanisms by which Ni ions increase lactate release and the role of lactate in enhancing the elution of Ni ions using a human fibroblast cell line, KMST-6. Results suggested that elution of Ni ions from metals promotes lactate production via HIF-1α-mediated gene expression and causes further Ni elution, indicating a positive feedback mechanism of Ni elution.These findings may provide insights for potential targets to protect against metal elution from metal devices.
Elution of Ni ions from medical devices induces inflammation and toxicity. We previously reported that elution of Ni ions from Ni wires induced COX-2 expression and increased lactate production, but whether lactate is involved in the further elution of Ni ions remains unclear. In this study, using KMST-6, a human fibroblast cell line, we examined the molecular mechanisms by which Ni ions increase lactate release and the role of lactate in enhancing the elution of Ni ions. When KMST-6 cells were incubated on a Ni plate or stimulated with NiCl2 (1 mM), the expression of glucose transporter 1 (GLUT1), hexokinase 2 (HK2), and lactate dehydrogenase A (LDHA), and the release of lactate were enhanced. The NiCl2 (1 mM)-induced expression of these genes was inhibited by a hypoxia-inducible factor-1 alpha (HIF-1 alpha) inhibitor, PX-478 (10-25 mu M). Stimulation of cells with a prolyl hydroxylase domain (PHD) inhibitor, roxadustat, increased the expression of these genes, lactate release, and elution of Ni ions at 10 mu M. A monocarboxylate transporter-4 (MCT4) inhibitor, syrosingopine, inhibited lactate release from roxadustat-treated cells and reduced the elution of Ni ions by the cells at 10 mu M. Finally, syrosingopine (10 mu M) reduced the elution of Ni ions by the cells from the Ni plate. These results suggest that elution of Ni ions from metals promotes the production of lactate via HIF-1 alpha-mediated gene expression and causes further Ni elution. Thus, Ni ions show a positive feedback mechanism of Ni elution, and this step may be potentially targeted to protect against metal elution from metal devices.

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