Vitamin D Receptor Deficiency Upregulates Pulmonary Artery Kv7 Channel Activity

Int J Mol Sci. 2023 Aug 2;24(15):12350. doi: 10.3390/ijms241512350.

Abstract

Recent evidence suggests that vitamin D is involved in the development of pulmonary arterial hypertension (PAH). The aim of this study was to analyze the electrophysiological and contractile properties of pulmonary arteries (PAs) in vitamin D receptor knockout mice (Vdr-/-). PAs were dissected and mounted in a wire myograph. Potassium membrane currents were recorded in freshly isolated PA smooth muscle cells (PASMCs) using the conventional whole-cell configuration of the patch-clamp technique. Potential vitamin D response elements (VDREs) in Kv7 channels coding genes were studied, and their protein expression was analyzed. Vdr-/- mice did not show a pulmonary hypertensive phenotype, as neither right ventricular hypertrophy nor endothelial dysfunction was apparent. However, resistance PA from these mice exhibited increased response to retigabine, a Kv7 activator, compared to controls and heterozygous mice. Furthermore, the current sensitive to XE991, a Kv7 inhibitor, was also higher in PASMCs from knockout mice. A possible VDRE was found in the gene coding for KCNE4, the regulatory subunit of Kv7.4. Accordingly, Vdr-/- mice showed an increased expression of KCNE4 in the lungs, with no changes in Kv7.1 and Kv7.4. These results indicate that the absence of Vdr in mice, as occurred with vitamin D deficient rats, is not sufficient to induce PAH. However, the contribution of Kv7 channel currents to the regulation of PA tone is increased in Vdr-/- mice, resembling animals and humans suffering from PAH.

Keywords: KCNE; Kv7 channels; pulmonary hypertension; vitamin D receptor.

MeSH terms

  • Animals
  • Humans
  • KCNQ Potassium Channels / metabolism
  • Mice
  • Mice, Knockout
  • Muscle, Smooth, Vascular / metabolism
  • Potassium Channels, Voltage-Gated* / metabolism
  • Pulmonary Artery* / metabolism
  • Rats
  • Receptors, Calcitriol / genetics
  • Receptors, Calcitriol / metabolism
  • Vitamin D / metabolism
  • Vitamin D / pharmacology

Substances

  • KCNE4 protein, mouse
  • KCNQ Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Receptors, Calcitriol
  • Vitamin D
  • VDR protein, human