New insights into Vitamin C function: Vitamin C induces JAK2 activation through its receptor-like transporter SVCT2

Int J Biol Macromol. 2021 Mar 15:173:379-398. doi: 10.1016/j.ijbiomac.2021.01.120. Epub 2021 Jan 20.

Abstract

Vitamin C (VitC) is a requisite nutrient for humans and other primates. Extensive research continuously illustrates the applications of VitC in promoting cell reprogramming, fine-tuning embryonic stem cell function, and fighting diseases. Given its chemical reduction property, VitC predominantly acts as an antioxidant to reduce reactive oxygen species (ROS) and as a cofactor for certain dioxygenases involved in epigenetic regulation. Here, we propose that VitC is also a bio-signaling molecule based on the finding that sodium-dependent VitC transporter (SVCT) 2 is a novel receptor-like transporter of VitC that possesses dual activities in mediating VitC uptake and Janus kinase (JAK) 2/signal transducer and activator of transcription (STAT) 2 signaling pathway. Through interaction, SVCT2 induces JAK2 phosphorylation while transporting VitC into cells. Activated JAK2 phosphorylates the C-terminus of SVCT2, resulting in the recruitment and activation of STAT2. As a highlight, our results suggest that the activation of JAK2 synergistically promotes regulation of VitC in ROS scavenging and epigenetic modifications through phosphorylating pyruvate dehydrogenase kinase 1, ten-eleven translocation enzyme 3, and histone H3 Tyr41. Furthermore, VitC-activated JAK2 exhibits bidirectional effects in regulating cell pluripotency and differentiation. Our results thus reveal that the SVCT2-mediated JAK2 activation facilitates VitC functions in a previously unknown manner.

Keywords: JAK2; SVCT2; TET3; Tyrosine phosphorylation; Vitamin C.

MeSH terms

  • Animals
  • Ascorbic Acid / metabolism*
  • Ascorbic Acid / pharmacology
  • Cell Differentiation / drug effects
  • Cell Line
  • Dioxygenases / genetics
  • Epigenesis, Genetic / drug effects
  • HEK293 Cells
  • Histones / metabolism
  • Humans
  • Janus Kinase 2 / metabolism*
  • Mice
  • NIH 3T3 Cells
  • Phosphorylation
  • Protein Domains
  • STAT2 Transcription Factor / genetics
  • Signal Transduction / drug effects
  • Sodium-Coupled Vitamin C Transporters / chemistry
  • Sodium-Coupled Vitamin C Transporters / genetics*
  • Sodium-Coupled Vitamin C Transporters / metabolism*

Substances

  • Histones
  • SLC23A2 protein, human
  • STAT2 Transcription Factor
  • STAT2 protein, human
  • Sodium-Coupled Vitamin C Transporters
  • TET3 protein, human
  • Dioxygenases
  • JAK2 protein, human
  • Janus Kinase 2
  • Ascorbic Acid