Retrotransposons are co-opted to activate hematopoietic stem cells and erythropoiesis

Science. 2024 Nov 8;386(6722):eado6836. doi: 10.1126/science.ado6836. Epub 2024 Nov 8.

Abstract

Hematopoietic stem cells (HSCs) and erythropoiesis are activated during pregnancy and after bleeding by the derepression of retrotransposons, including endogenous retroviruses and long interspersed nuclear elements. Retrotransposon transcription activates the innate immune sensors cyclic guanosine 3',5'-monophosphate-adenosine 5'-monophosphate synthase (cGAS) and stimulator of interferon (IFN) genes (STING), which induce IFN and IFN-regulated genes in HSCs, increasing HSC division and erythropoiesis. Inhibition of reverse transcriptase or deficiency for cGAS or STING had little or no effect on hematopoiesis in nonpregnant mice but depleted HSCs and erythroid progenitors in pregnant mice, reducing red blood cell counts. Retrotransposons and IFN-regulated genes were also induced in mouse HSCs after serial bleeding and, in human HSCs, during pregnancy. Reverse transcriptase inhibitor use was associated with anemia in pregnant but not in nonpregnant people, suggesting conservation of these mechanisms from mice to humans.

MeSH terms

  • Anemia / genetics
  • Animals
  • Erythropoiesis* / genetics
  • Female
  • Hematopoietic Stem Cells* / metabolism
  • Hemorrhage / genetics
  • Humans
  • Interferons / genetics
  • Interferons / metabolism
  • Long Interspersed Nucleotide Elements
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nucleotidyltransferases / genetics
  • Nucleotidyltransferases / metabolism
  • Pregnancy
  • Retroelements* / genetics
  • Transcription, Genetic

Substances

  • Interferons
  • Membrane Proteins
  • Nucleotidyltransferases
  • Retroelements
  • Sting1 protein, mouse