Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha

FASEB J. 2024 Jan;38(1):e23346. doi: 10.1096/fj.202300202R.

Abstract

Folate deficiency contribute to neural tube defects (NTDs) which could be rescued by folate supplementation. However, the underlying mechanisms are still not fully understood. Besides, there is considerable controversy concerning the forms of folate used for supplementation. To address this controversy, we prepared culture medium with different forms of folate, folic acid (FA), and 5-methyltetrahydrofolate (5mTHF), at concentrations of 5 μM, 500 nM, 50 nM, and folate free, respectively. Mouse embryonic fibroblasts (MEFs) were treated with different folates continuously for three passages, and cell proliferation and F-actin were monitored. We determined that compared to 5mTHF, FA showed stronger effects on promoting cell proliferation and F-actin formation. We also found that FOLR1 protein level was positively regulated by folate concentration and the non-canonical Wnt/planar cell polarity (PCP) pathway signaling was significantly enriched among different folate conditions in RNA-sequencing analyses. We demonstrated for the first time that FOLR1 could promote the transcription of Vangl2, one of PCP core genes. The transcription of Vangl2 was down-regulated under folate-deficient condition, which resulted in a decrease in PCP activity and F-actin formation. In summary, we identified a distinct advantage of FA in cell proliferation and F-actin formation over 5mTHF, as well as demonstrating that FOLR1 could promote transcription of Vangl2 and provide a new mechanism by which folate deficiency can contribute to the etiology of NTDs.

Keywords: 5-methyltetrahydrofolate; F-actin; FOLR1; PCP signaling pathway; Vangl2; folic acid.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Polarity / genetics
  • Fibroblasts / metabolism
  • Folate Receptor 1 / genetics
  • Folate Receptor 1 / metabolism
  • Folic Acid / metabolism
  • Folic Acid Deficiency* / metabolism
  • Mice
  • Neural Tube Defects* / genetics
  • Neural Tube Defects* / metabolism
  • Wnt Signaling Pathway

Substances

  • Folic Acid
  • Actins
  • Folate Receptor 1