Single-cell transcriptomics reveal the dynamic of haematopoietic stem cell production in the aorta. 2018

Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
Hubrecht Institute-KNAW, University Medical Center Utrecht, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.

Haematopoietic stem cells (HSCs) are generated from haemogenic endothelial (HE) cells via the formation of intra-aortic haematopoietic clusters (IAHCs) in vertebrate embryos. The molecular events controlling endothelial specification, endothelial-to-haematopoietic transition (EHT) and IAHC formation, as it occurs in vivo inside the aorta, are still poorly understood. To gain insight in these processes, we performed single-cell RNA-sequencing of non-HE cells, HE cells, cells undergoing EHT, IAHC cells, and whole IAHCs isolated from mouse embryo aortas. Our analysis identified the genes and transcription factor networks activated during the endothelial-to-haematopoietic switch and IAHC cell maturation toward an HSC fate. Our study provides an unprecedented complete resource to study in depth HSC generation in vivo. It will pave the way for improving HSC production in vitro to address the growing need for tailor-made HSCs to treat patients with blood-related disorders.

UI MeSH Term Description Entries
D008810 Mice, Inbred C57BL One of the first INBRED MOUSE STRAINS to be sequenced. This strain is commonly used as genetic background for transgenic mouse models. Refractory to many tumors, this strain is also preferred model for studying role of genetic variations in development of diseases. Mice, C57BL,Mouse, C57BL,Mouse, Inbred C57BL,C57BL Mice,C57BL Mice, Inbred,C57BL Mouse,C57BL Mouse, Inbred,Inbred C57BL Mice,Inbred C57BL Mouse
D002454 Cell Differentiation Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs. Differentiation, Cell,Cell Differentiations,Differentiations, Cell
D004622 Embryo, Mammalian The entity of a developing mammal (MAMMALS), generally from the cleavage of a ZYGOTE to the end of embryonic differentiation of basic structures. For the human embryo, this represents the first two months of intrauterine development preceding the stages of the FETUS. Embryonic Structures, Mammalian,Mammalian Embryo,Mammalian Embryo Structures,Mammalian Embryonic Structures,Embryo Structure, Mammalian,Embryo Structures, Mammalian,Embryonic Structure, Mammalian,Embryos, Mammalian,Mammalian Embryo Structure,Mammalian Embryonic Structure,Mammalian Embryos,Structure, Mammalian Embryo,Structure, Mammalian Embryonic,Structures, Mammalian Embryo,Structures, Mammalian Embryonic
D005260 Female Females
D006412 Hematopoietic Stem Cells Progenitor cells from which all blood cells derived. They are found primarily in the bone marrow and also in small numbers in the peripheral blood. Colony-Forming Units, Hematopoietic,Progenitor Cells, Hematopoietic,Stem Cells, Hematopoietic,Hematopoietic Progenitor Cells,Cell, Hematopoietic Progenitor,Cell, Hematopoietic Stem,Cells, Hematopoietic Progenitor,Cells, Hematopoietic Stem,Colony Forming Units, Hematopoietic,Colony-Forming Unit, Hematopoietic,Hematopoietic Colony-Forming Unit,Hematopoietic Colony-Forming Units,Hematopoietic Progenitor Cell,Hematopoietic Stem Cell,Progenitor Cell, Hematopoietic,Stem Cell, Hematopoietic,Unit, Hematopoietic Colony-Forming,Units, Hematopoietic Colony-Forming
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001011 Aorta The main trunk of the systemic arteries. Aortas
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus
D053263 Gene Regulatory Networks Interacting DNA-encoded regulatory subsystems in the GENOME that coordinate input from activator and repressor TRANSCRIPTION FACTORS during development, cell differentiation, or in response to environmental cues. The networks function to ultimately specify expression of particular sets of GENES for specific conditions, times, or locations. Gene Circuits,Gene Modules,Gene Networks,Transcriptional Networks,Gene Module,Circuit, Gene,Circuits, Gene,Gene Circuit,Gene Network,Gene Regulatory Network,Module, Gene,Modules, Gene,Network, Gene,Network, Gene Regulatory,Network, Transcriptional,Networks, Gene,Networks, Gene Regulatory,Networks, Transcriptional,Regulatory Network, Gene,Regulatory Networks, Gene,Transcriptional Network
D055018 Hemangioblasts Bipotential angio-hematopoietic stem cells that give rise to both HEMATOPOIETIC STEM CELLS and ENDOTHELIAL CELLS. Hemangioblast,Hemogenic Endothelial Cells,Hemogenic Endothelium,Cell, Hemogenic Endothelial,Cells, Hemogenic Endothelial,Endothelial Cell, Hemogenic,Endothelial Cells, Hemogenic,Endothelium, Hemogenic,Endotheliums, Hemogenic,Hemogenic Endothelial Cell,Hemogenic Endotheliums

Related Publications

Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
October 2021, Cell death & disease,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
January 2023, Development (Cambridge, England),
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
June 2020, Nature,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
May 2021, Cancer discovery,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
April 2023, eLife,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
May 2016, Nature,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
May 2015, Molecular cell,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
January 2020, Nature cell biology,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
September 2021, Molecular therapy oncolytics,
Chloé S Baron, and Lennart Kester, and Anna Klaus, and Jean-Charles Boisset, and Roshana Thambyrajah, and Laurent Yvernogeau, and Valérie Kouskoff, and Georges Lacaud, and Alexander van Oudenaarden, and Catherine Robin
November 2023, Nature communications,
Copied contents to your clipboard!