SARS-CoV-2 infection causes a decline in renal megalin expression and affects vitamin D metabolism in the kidney of K18-hACE2 mice

Sci Rep. 2024 Oct 16;14(1):24313. doi: 10.1038/s41598-024-75338-9.

Abstract

Patients with coronavirus disease 2019 (COVID-19) often experience acute kidney injury, linked to disease severity or mortality, along with renal tubular dysfunction and megalin loss in proximal tubules. Megalin plays a crucial role in kidney vitamin D metabolism. However, the impact of megalin loss on vitamin D metabolism during COVID-19 is unclear. This study investigated whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection reduces megalin expression in proximal tubules and its subsequent effect on vitamin D metabolism in mice expressing human angiotensin converting enzyme 2 (K18-hACE2 mice). Histological and immunohistochemical staining analyses revealed glomerular and capillary congestion, and elevated renal neutrophil gelatinase-associated lipocalin levels, indicative of acute kidney injury in K18-hACE2 mice. In SARS-CoV-2-infected mice, immunohistochemical staining revealed suppressed megalin protein levels. Decreased vitamin D receptor (VDR) localization in the nucleus and increased mRNA expression of VDR, CYP27B1, and CYP24A1 were observed by quantitative PCR in SARS-CoV-2-infected mice. Serum vitamin D levels remained similar in infected and vehicle-treated mice, but an increase in tumor necrosis factor-alpha and a decrease in IL-4 mRNA expression were observed in the kidneys of the SARS-CoV-2 group. These findings suggest that megalin loss in SARS-CoV-2 infection may impact the local role of vitamin D in kidney immunomodulation, even when blood vitamin D levels remain unchanged.

MeSH terms

  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / metabolism
  • Acute Kidney Injury / pathology
  • Acute Kidney Injury / virology
  • Angiotensin-Converting Enzyme 2 / genetics
  • Angiotensin-Converting Enzyme 2 / metabolism
  • Animals
  • COVID-19* / genetics
  • COVID-19* / metabolism
  • COVID-19* / virology
  • Disease Models, Animal
  • Humans
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Tubules, Proximal / metabolism
  • Kidney Tubules, Proximal / virology
  • Low Density Lipoprotein Receptor-Related Protein-2* / genetics
  • Low Density Lipoprotein Receptor-Related Protein-2* / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Receptors, Calcitriol / genetics
  • Receptors, Calcitriol / metabolism
  • SARS-CoV-2
  • Vitamin D* / metabolism

Substances

  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Lrp2 protein, mouse
  • Receptors, Calcitriol
  • Vitamin D