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Transcription factor induction of vascular blood stem cell niches in vivo

Authors :
Hagedorn, Elliott J
Perlin, Julie R
Freeman, Rebecca J
Wattrus, Samuel J
Han, Tianxiao
Mao, Clara
Kim, Ji Wook
Fernández-Maestre, Inés
Daily, Madeleine L
D'Amato, Christopher
Fairchild, Michael J
Riquelme, Raquel
Li, Brian
Ragoonanan, Dana A V E
Enkhbayar, Khaliun
Henault, Emily L
Wang, Helen G
Redfield, Shelby E
Collins, Samantha H
Lichtig, Asher
Yang, Song
Zhou, Yi
Kunar, Balvir
Gomez-Salinero, Jesus Maria
Dinh, Thanh T
Pan, Junliang
Holler, Karoline
Feldman, Henry A
Butcher, Eugene C
van Oudenaarden, Alexander
Rafii, Shahin
Junker, J Philipp
Zon, Leonard I
Hagedorn, Elliott J
Perlin, Julie R
Freeman, Rebecca J
Wattrus, Samuel J
Han, Tianxiao
Mao, Clara
Kim, Ji Wook
Fernández-Maestre, Inés
Daily, Madeleine L
D'Amato, Christopher
Fairchild, Michael J
Riquelme, Raquel
Li, Brian
Ragoonanan, Dana A V E
Enkhbayar, Khaliun
Henault, Emily L
Wang, Helen G
Redfield, Shelby E
Collins, Samantha H
Lichtig, Asher
Yang, Song
Zhou, Yi
Kunar, Balvir
Gomez-Salinero, Jesus Maria
Dinh, Thanh T
Pan, Junliang
Holler, Karoline
Feldman, Henry A
Butcher, Eugene C
van Oudenaarden, Alexander
Rafii, Shahin
Junker, J Philipp
Zon, Leonard I
Source :
Developmental Cell vol.58 (2023) date: 2023-06-19 nr.12 p.1037-1051.e4 [ISSN 1534-5807]
Publication Year :
2023

Abstract

The hematopoietic niche is a supportive microenvironment composed of distinct cell types, including specialized vascular endothelial cells that directly interact with hematopoietic stem and progenitor cells (HSPCs). The molecular factors that specify niche endothelial cells and orchestrate HSPC homeostasis remain largely unknown. Using multi-dimensional gene expression and chromatin accessibility analyses in zebrafish, we define a conserved gene expression signature and cis-regulatory landscape that are unique to sinusoidal endothelial cells in the HSPC niche. Using enhancer mutagenesis and transcription factor overexpression, we elucidate a transcriptional code that involves members of the Ets, Sox, and nuclear hormone receptor families and is sufficient to induce ectopic niche endothelial cells that associate with mesenchymal stromal cells and support the recruitment, maintenance, and division of HSPCs in vivo. These studies set forth an approach for generating synthetic HSPC niches, in vitro or in vivo, and for effective therapies to modulate the endogenous niche.

Details

Database :
OAIster
Journal :
Developmental Cell vol.58 (2023) date: 2023-06-19 nr.12 p.1037-1051.e4 [ISSN 1534-5807]
Notes :
DOI: 10.1016/j.devcel.2023.04.007, Developmental Cell vol.58 (2023) date: 2023-06-19 nr.12 p.1037-1051.e4 [ISSN 1534-5807], English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1419112910
Document Type :
Electronic Resource