Cited2 is an essential regulator of adult hematopoietic stem cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 19951693.
- Also identified by DOI 10.1016/j.stem.2009.11.001 and PMC identifier 2828538.
- 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
The regulatory pathways necessary for the maintenance of adult hematopoietic stem cells (HSCs) remain poorly defined. By using loss-of-function approaches, we report a selective and cell-autonomous requirement for the p300/CBP-binding transcriptional coactivator Cited2 in adult HSC maintenance. Conditional deletion of Cited2 in the adult mouse results in loss of HSCs causing multilineage bone marrow failure and increased lethality. In contrast, conditional ablation of Cited2 after lineage specification in lymphoid and myeloid lineages has no impact on the maintenance of these lineages. Additional deletion of Ink4a/Arf (encoding p16(Ink4a) and p19(Arf)) or Trp53 (encoding p53, a downstream target of p19(Arf)) in a Cited2-deficient background restores HSC functionality and rescues mice from bone marrow failure. Furthermore, we show that the critical role of Cited2 in primitive hematopoietic cells is conserved in humans. Taken together, our studies provide genetic evidence that Cited2 selectively maintains adult HSC functions, at least in part, via Ink4a/Arf and Trp53.
Medical subject headings
- ADP-Ribosylation Factors
- Adult Stem Cells
- Cyclin-Dependent Kinase Inhibitor p16
- Hematopoietic Stem Cells
- Repressor Proteins
- Trans-Activators
- Tumor Suppressor Protein p53