ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2022 and some content may be unavailable. To unlock all content for 2022, please visit the archives.

Abstract: FR-PO384

Malnutrition During Pregnancy Impairs Nephrogenesis by Modifying Epigenetic Regulation in Nephron Progenitor Cells

Session Information

Category: Development‚ Stem Cells‚ and Regenerative Medicine

  • 500 Development‚ Stem Cells‚ and Regenerative Medicine

Authors

  • Volovelsky, Oded, Hadassah University Medical Center, Jerusalem, Jerusalem, Israel
  • Makayes, Yaniv, Hadassah University Medical Center, Jerusalem, Jerusalem, Israel
  • Nechama, Morris, Hadassah University Medical Center, Jerusalem, Jerusalem, Israel
Background

Poor intrauterine environment, such as maternal malnutrition, impairs nephron endowment and increases the risk of chronic kidney disease in adulthood in the next generation. We have previously demonstrated that methionine metabolism has an important role in mediating the negative effects of caloric restriction during pregnancy on nephron endowment. As methionine has an important role in epigenetic control of gene expression, we examined the effects of malnutrition on gene methylation in nephron progenitor cells.

Methods

The caloric intake of pregnant mice was limited to 70% of daily intake. Nephron progenitor cells (NPCs) were sorted using transgenic mice with specific GFP labeling. DNA from NPCs was extracted, and the methylation pattern was characterized and analyzed using reduced representation bisulfite sequencing. The data acquired was cross-referenced with chromatin accessibility and histone modification data of nephron progenitor cells. The findings were validated using RT-qPCR. In addition, the effects of methionine on methylation patterns were evaluated using Bisulfite Amplicon Sequencing.

Results

Caloric restriction during pregnancy leads to a global decrease in DNA methylation in nephron progenitor cells compared to control. Specific changes in DNA methylation were localized to gene promoters, enhancers, and transcription factor binding sites. These effects were present throughout the genome, including genes involved in nephrogenesis and pivotal intracellular signaling pathways, in accordance with the changes in expression profile.

Conclusion

This study is the first evidence that maternal malnutrition during pregnancy impairs nephrogenesis by modifying epigenetic remodeling in NPCs, presumably mediated by methionine.

Heatmaps of differentially methylated regions in DNA of NPCs extracted from embryonic kidneys subjected to caloric restriction during pregnancy. Pie charts representing the anticipated distribution of differentially methylated regions.