Regulation of stem cell function and neuronal differentiation by HERV-K via mTOR pathway

Proc Natl Acad Sci U S A. 2020 Jul 28;117(30):17842-17853. doi: 10.1073/pnas.2002427117. Epub 2020 Jul 15.

Abstract

Stem cells are capable of unlimited proliferation but can be induced to form brain cells. Factors that specifically regulate human development are poorly understood. We found that human stem cells expressed high levels of the envelope protein of an endogenized human-specific retrovirus (HERV-K, HML-2) from loci in chromosomes 12 and 19. The envelope protein was expressed on the cell membrane of the stem cells and was critical in maintaining the stemness via interactions with CD98HC, leading to triggering of human-specific signaling pathways involving mammalian target of rapamycin (mTOR) and lysophosphatidylcholine acyltransferase (LPCAT1)-mediated epigenetic changes. Down-regulation or epigenetic silencing of HML-2 env resulted in dissociation of the stem cell colonies and enhanced differentiation along neuronal pathways. Thus HML-2 regulation is critical for human embryonic and neurodevelopment, while it's dysregulation may play a role in tumorigenesis and neurodegeneration.

Keywords: embryogenesis; endogenous retrovirus; neurogenesis; progenitor cells; stem cells.

Publication types

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

MeSH terms

  • Biomarkers
  • Cell Differentiation* / genetics
  • Cell Self Renewal / genetics
  • Endogenous Retroviruses / physiology*
  • Fusion Regulatory Protein 1, Heavy Chain / metabolism
  • Gene Expression Regulation, Viral
  • Humans
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Neurons / cytology
  • Neurons / metabolism*
  • Protein Binding
  • Signal Transduction*
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • TOR Serine-Threonine Kinases / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Viral Envelope Proteins / genetics

Substances

  • Biomarkers
  • Fusion Regulatory Protein 1, Heavy Chain
  • SLC3A2 protein, human
  • Transcription Factors
  • Viral Envelope Proteins
  • MTOR protein, human
  • TOR Serine-Threonine Kinases