| Literature DB >> 32149421 |
Cristina Porcheri1, Ohad Golan2, Fernando J Calero-Nieto3, Roshana Thambyrajah1, Cristina Ruiz-Herguido1, Xiaonan Wang3, Francesca Catto1, Yolanda Guillén1, Roshani Sinha1, Jessica González1, Sarah J Kinston3, Samanta A Mariani4, Antonio Maglitto4, Chris S Vink4, Elaine Dzierzak4, Pierre Charbord5, Bertie Göttgens3, Lluis Espinosa1, David Sprinzak2, Anna Bigas1.
Abstract
Hematopoietic stem cells (HSCs) develop from the hemogenic endothelium in cluster structures that protrude into the embryonic aortic lumen. Although much is known about the molecular characteristics of the developing hematopoietic cells, we lack a complete understanding of their origin and the three-dimensional organization of the niche. Here, we use advanced live imaging techniques of organotypic slice cultures, clonal analysis, and mathematical modeling to show the two-step process of intra-aortic hematopoietic cluster (IACH) formation. First, a hemogenic progenitor buds up from the endothelium and undergoes division forming the monoclonal core of the IAHC. Next, surrounding hemogenic cells are recruited into the IAHC, increasing their size and heterogeneity. We identified the Notch ligand Dll4 as a negative regulator of the recruitment phase of IAHC. Blocking of Dll4 promotes the entrance of new hemogenic Gfi1+ cells into the IAHC and increases the number of cells that acquire HSC activity. Mathematical modeling based on our data provides estimation of the cluster lifetime and the average recruitment time of hemogenic cells to the cluster under physiologic and Dll4-inhibited conditions.Entities:
Keywords: zzm321990AGMzzm321990; zzm321990HSCzzm321990; Dll4; Notch; hemogenic endothelium
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Year: 2020 PMID: 32149421 PMCID: PMC7156969 DOI: 10.15252/embj.2019104270
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598