Transcripts of repetitive DNA elements signal to block phagocytosis of hematopoietic stem cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39264994.
- Also identified by DOI 10.1126/science.adn1629 and PMC identifier 12012832.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Macrophages maintain hematopoietic stem cell (HSC) quality by assessing cell surface Calreticulin (Calr), an "eat-me" signal induced by reactive oxygen species (ROS). Using zebrafish genetics, we identified Beta-2-microglobulin (B2m) as a crucial "don't eat-me" signal on blood stem cells. A chemical screen revealed inducers of surface Calr that promoted HSC proliferation without triggering ROS or macrophage clearance. Whole-genome CRISPR-Cas9 screening showed that Toll-like receptor 3 (Tlr3) signaling regulated <i>b2m</i> expression. Targeting <i>b2m</i> or <i>tlr3</i> reduced the HSC clonality. Elevated B2m levels correlated with high expression of repetitive element (RE) transcripts. Overall, our data suggest that RE-associated double-stranded RNA could interact with TLR3 to stimulate surface expression of B2m on hematopoietic stem and progenitor cells. These findings suggest that the balance of Calr and B2m regulates macrophage-HSC interactions and defines hematopoietic clonality.
Medical subject headings
- beta 2-Microglobulin
- Calreticulin
- Hematopoietic Stem Cells
- Macrophages
- Phagocytosis
- Toll-Like Receptor 3