Primary cilia regulate hematopoietic stem and progenitor cell specification through Notch signaling in zebrafish.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31015398.
- Also identified by DOI 10.1038/s41467-019-09403-7 and PMC identifier 6478842.
- 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
Hematopoietic stem and progenitor cells (HSPCs) are capable of producing all mature blood lineages, as well as maintaining the self-renewal ability throughout life. The hairy-like organelle, cilium, is present in most types of vertebrate cells, and plays important roles in various biological processes. However, it is unclear whether and how cilia regulate HSPC development in vertebrates. Here, we show that cilia-specific genes, involved in primary cilia formation and function, are required for HSPC development, especially in hemogenic endothelium (HE) specification in zebrafish embryos. Blocking primary cilia formation or function by genetic or chemical manipulations impairs HSPC development. Mechanistically, we uncover that primary cilia in endothelial cells transduce Notch signal to the earliest HE for proper HSPC specification during embryogenesis. Altogether, our findings reveal a pivotal role of endothelial primary cilia in HSPC development, and may shed lights into in vitro directed differentiation of HSPCs.
Medical subject headings
- Cilia
- Hematopoietic Stem Cells
- Receptors, Notch
- Signal Transduction
- Zebrafish Proteins