Author
Listed:
- Zhibin Liu
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Chinese Academy of Sciences)
- Haiqing Tu
(National Center of Biomedical Analysis)
- Yunsi Kang
(Ocean University of China)
- Yuanyuan Xue
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Chinese Academy of Sciences)
- Dongyuan Ma
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Chinese Academy of Sciences)
- Chengtian Zhao
(Ocean University of China)
- Huiyan Li
(National Center of Biomedical Analysis)
- Lu Wang
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Chinese Academy of Medical Sciences & Peking Union Medical College)
- Feng Liu
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Chinese Academy of Sciences)
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.
Suggested Citation
Zhibin Liu & Haiqing Tu & Yunsi Kang & Yuanyuan Xue & Dongyuan Ma & Chengtian Zhao & Huiyan Li & Lu Wang & Feng Liu, 2019.
"Primary cilia regulate hematopoietic stem and progenitor cell specification through Notch signaling in zebrafish,"
Nature Communications, Nature, vol. 10(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09403-7
DOI: 10.1038/s41467-019-09403-7
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09403-7. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.