CD32 captures committed haemogenic endothelial cells during human embryonic development.


Journal

Nature cell biology
ISSN: 1476-4679
Titre abrégé: Nat Cell Biol
Pays: England
ID NLM: 100890575

Informations de publication

Date de publication:
09 Apr 2024
Historique:
received: 06 04 2023
accepted: 07 03 2024
medline: 10 4 2024
pubmed: 10 4 2024
entrez: 9 4 2024
Statut: aheadofprint

Résumé

During embryonic development, blood cells emerge from specialized endothelial cells, named haemogenic endothelial cells (HECs). As HECs are rare and only transiently found in early developing embryos, it remains difficult to distinguish them from endothelial cells. Here we performed transcriptomic analysis of 28- to 32-day human embryos and observed that the expression of Fc receptor CD32 (FCGR2B) is highly enriched in the endothelial cell population that contains HECs. Functional analyses using human embryonic and human pluripotent stem cell-derived endothelial cells revealed that robust multilineage haematopoietic potential is harboured within CD32

Identifiants

pubmed: 38594587
doi: 10.1038/s41556-024-01403-0
pii: 10.1038/s41556-024-01403-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : INV-002414
Pays : United States

Informations de copyright

© 2024. The Author(s).

Références

Jaffredo, T., Gautier, R., Eichmann, A. & Dieterlen-Lièvre, F. Intraaortic hemopoietic cells are derived from endothelial cells during ontogeny. Development 125, 4575–4583 (1998).
pubmed: 9778515 doi: 10.1242/dev.125.22.4575
DeBruijn, M. F. T. R., Speck, N. A., Peeters, M. C. E. & Dzierzak, E. Definitive hematopoietic stem cells first develop within the major arterial regions of the mouse embryo. EMBO J. 19, 2465–2474 (2000).
doi: 10.1093/emboj/19.11.2465
Oberlin, E., Tavian, M., Blazsek, I. & Péault, B. Blood-forming potential of vascular endothelium in the human embryo. Development 129, 4147–4157 (2002).
pubmed: 12163416 doi: 10.1242/dev.129.17.4147
Zovein, A. C. et al. Fate tracing reveals the endothelial origin of hematopoietic stem cells. Cell Stem Cell 3, 625–636 (2008).
pubmed: 19041779 pmcid: 2631552 doi: 10.1016/j.stem.2008.09.018
Bertrand, J. Y. et al. Haematopoietic stem cells derive directly from aortic endothelium during development. Nature 464, 108–111 (2010).
pubmed: 20154733 pmcid: 2858358 doi: 10.1038/nature08738
Boisset, J.-C. et al. In vivo imaging of haematopoietic cells emerging from the mouse aortic endothelium. Nature 464, 116–120 (2010).
pubmed: 20154729 doi: 10.1038/nature08764
Kissa, K. & Herbomel, P. Blood stem cells emerge from aortic endothelium by a novel type of cell transition. Nature 464, 112–115 (2010).
pubmed: 20154732 doi: 10.1038/nature08761
Lancrin, C. et al. The haemangioblast generates haematopoietic cells through a haemogenic endothelium stage. Nature 457, 892–895 (2009).
pubmed: 19182774 pmcid: 2661201 doi: 10.1038/nature07679
Frame, J. M., Fegan, K. H., Conway, S. J., McGrath, K. E. & Palis, J. Definitive hematopoiesis in the yolk sac emerges from Wnt‐responsive hemogenic endothelium independently of circulation and arterial identity. Stem Cells 34, 431–444 (2016).
pubmed: 26418893 doi: 10.1002/stem.2213
Stefanska, M. et al. Primitive erythrocytes are generated from hemogenic endothelial cells. Sci. Rep. 7, 6401 (2017).
pubmed: 28743905 pmcid: 5526883 doi: 10.1038/s41598-017-06627-9
Souilhol, C. et al. Developing HSCs become Notch independent by the end of maturation in the AGM region. Blood 128, 1567–1577 (2016).
pubmed: 27421959 pmcid: 5034738 doi: 10.1182/blood-2016-03-708164
Robert-Moreno, A., Espinosa, L., de la Pompa, J. L. & Bigas, A. RBPjκ-dependent Notch function regulates Gata2 and is essential for the formation of intra-embryonic hematopoietic cells. Development 132, 1117–1126 (2005).
pubmed: 15689374 doi: 10.1242/dev.01660
Robert‐Moreno, À. et al. Impaired embryonic haematopoiesis yet normal arterial development in the absence of the Notch ligand Jagged1. EMBO J. 27, 1886–1895 (2008).
pubmed: 18528438 pmcid: 2486417 doi: 10.1038/emboj.2008.113
Ditadi, A. et al. Human definitive haemogenic endothelium and arterial vascular endothelium represent distinct lineages. Nat. Cell Biol. 17, 580–591 (2015).
pubmed: 25915127 pmcid: 4551438 doi: 10.1038/ncb3161
North, T. et al. Cbfa2 is required for the formation of intra-aortic hematopoietic clusters. Development 126, 2563–2575 (1999).
pubmed: 10226014 doi: 10.1242/dev.126.11.2563
Swiers, G. et al. Early dynamic fate changes in haemogenic endothelium characterized at the single-cell level. Nat. Commun. 4, 2924 (2013).
pubmed: 24326267 doi: 10.1038/ncomms3924
Thambyrajah, R. et al. GFI1 proteins orchestrate the emergence of haematopoietic stem cells through recruitment of LSD1. Nat. Cell Biol. 18, 21–32 (2016).
pubmed: 26619147 doi: 10.1038/ncb3276
Jokubaitis, V. J. et al. Angiotensin-converting enzyme (CD143) marks hematopoietic stem cells in human embryonic, fetal, and adult hematopoietic tissues. Blood 111, 4055–4063 (2008).
pubmed: 17993616 doi: 10.1182/blood-2007-05-091710
Sinka, L., Biasch, K., Khazaal, I., Péault, B. & Tavian, M. Angiotensin-converting enzyme (CD143) specifies emerging lympho-hematopoietic progenitors in the human embryo. Blood 119, 3712–3723 (2012).
pubmed: 22282502 doi: 10.1182/blood-2010-11-314781
Zeng, Y. et al. Tracing the first hematopoietic stem cell generation in human embryo by single-cell RNA sequencing. Cell Res. 29, 881–894 (2019).
pubmed: 31501518 pmcid: 6888893 doi: 10.1038/s41422-019-0228-6
Oatley, M. et al. Single-cell transcriptomics identifies CD44 as a marker and regulator of endothelial to haematopoietic transition. Nat. Commun. 11, 586 (2020).
pubmed: 31996681 pmcid: 6989687 doi: 10.1038/s41467-019-14171-5
Fadlullah, M. Z. et al. Murine AGM single-cell profiling identifies a continuum of hemogenic endothelium differentiation marked by ACE. Blood https://doi.org/10.1182/blood.2020007885 (2021).
doi: 10.1182/blood.2020007885
Dignum, T. et al. Multipotent progenitors and hematopoietic stem cells arise independently from hemogenic endothelium in the mouse embryo. Cell Rep. 36, 109675 (2021).
pubmed: 34525376 pmcid: 8478150 doi: 10.1016/j.celrep.2021.109675
Yamamizu, K. et al. Convergence of Notch and β-catenin signaling induces arterial fate in vascular progenitors. J. Cell Biol. 189, 325–338 (2010).
pubmed: 20404113 pmcid: 2856895 doi: 10.1083/jcb.200904114
Tavian, M. et al. Aorta-associated CD34
pubmed: 8547678 doi: 10.1182/blood.V87.1.67.67
Tavian, M., Hallais, M. F. & Péault, B. Emergence of intraembryonic hematopoietic precursors in the pre-liver human embryo. Development 126, 793–803 (1999).
pubmed: 9895326 doi: 10.1242/dev.126.4.793
Ng, E. S. et al. Differentiation of human embryonic stem cells to HOXA
pubmed: 27748754 doi: 10.1038/nbt.3702
Ditadi, A., Sturgeon, C. M. & Keller, G. A view of human haematopoietic development from the Petri dish. Nat. Rev. Mol. Cell Biol. 18, 56–67 (2016).
pubmed: 27876786 doi: 10.1038/nrm.2016.127
Luff, S. A. et al. Identification of a retinoic acid-dependent haemogenic endothelial progenitor from human pluripotent stem cells. Nat. Cell Biol. https://doi.org/10.1038/s41556-022-00898-9 (2022).
Gao, P. et al. Transcriptional regulatory network controlling the ontogeny of hematopoietic stem cells. Gene Dev. 34, 950–964 (2020).
pubmed: 32499402 pmcid: 7328518 doi: 10.1101/gad.338202.120
Luo, W. et al. Arterialization requires the timely suppression of cell growth. Nature https://doi.org/10.1038/s41586-020-3018-x (2020).
Strauss, O., Phillips, A., Ruggiero, K., Bartlett, A. & Dunbar, P. R. Immunofluorescence identifies distinct subsets of endothelial cells in the human liver. Sci. Rep. 7, 44356 (2017).
pubmed: 28287163 pmcid: 5347010 doi: 10.1038/srep44356
Lyden, T. W. et al. The Fc receptor for IgG expressed in the villus endothelium of human placenta is FcγRIIb2. J. Immunol. 166, 3882–3889 (2001).
pubmed: 11238632 doi: 10.4049/jimmunol.166.6.3882
Gröger, M., Sarmay, G., Fiebiger, E., Wolff, K. & Petzelbauer, P. Dermal microvascular endothelial cells express CD32 receptors in vivo and in vitro. J. Immunol. 156, 1549–1556 (1996).
pubmed: 8568259 doi: 10.4049/jimmunol.156.4.1549
McGrath, K. E. et al. Distinct sources of hematopoietic progenitors emerge before HSCs and provide functional blood cells in the mammalian embryo. Cell Rep. 11, 1892–1904 (2015).
pubmed: 26095363 pmcid: 4490098 doi: 10.1016/j.celrep.2015.05.036
Sturgeon, C. M., Ditadi, A., Awong, G., Kennedy, M. & Keller, G. Wnt signaling controls the specification of definitive and primitive hematopoiesis from human pluripotent stem cells. Nat. Biotechnol. 32, 554–561 (2014).
pubmed: 24837661 pmcid: 4152856 doi: 10.1038/nbt.2915
Atkins, M. H. et al. Modeling human yolk sac hematopoiesis with pluripotent stem cells. J. Exp. Med. 219, e20211924 (2021).
pubmed: 34928315 pmcid: 8693237 doi: 10.1084/jem.20211924
Calvanese, V. et al. Mapping human haematopoietic stem cells from haemogenic endothelium to birth. Nature https://doi.org/10.1038/s41586-022-04571-x (2022).
Zhou, J. et al. Combined single-cell profiling of lncRNAs and functional screening reveals that H19 is pivotal for embryonic hematopoietic stem cell development. Cell Stem Cell https://doi.org/10.1016/j.stem.2018.11.023 (2019).
doi: 10.1016/j.stem.2018.11.023 pubmed: 31883835 pmcid: 6900750
Saelens, W., Cannoodt, R., Todorov, H. & Saeys, Y. A comparison of single-cell trajectory inference methods. Nat. Biotechnol. 37, 547–554 (2019).
pubmed: 30936559 doi: 10.1038/s41587-019-0071-9
Kamimoto, K. et al. Dissecting cell identity via network inference and in silico gene perturbation. Nature https://doi.org/10.1038/s41586-022-05688-9 (2023).
Cai, X. et al. Runx1 deficiency decreases ribosome biogenesis and confers stress resistance to hematopoietic stem and progenitor cells. Cell Stem Cell 17, 165–177 (2015).
pubmed: 26165925 pmcid: 4530029 doi: 10.1016/j.stem.2015.06.002
Tiyaboonchai, A. et al. Utilization of the AAVS1 safe harbor locus for hematopoietic specific transgene expression and gene knockdown in human ES cells. Stem Cell Res. 12, 630–637 (2014).
pubmed: 24631742 pmcid: 4048956 doi: 10.1016/j.scr.2014.02.004
Dege, C. et al. Potently cytotoxic natural killer cells initially emerge from erythro-myeloid progenitors during mammalian development. Dev. Cell 53, 229–239.e7 (2020).
pubmed: 32197069 pmcid: 7185477 doi: 10.1016/j.devcel.2020.02.016
Canu, G. et al. Analysis of endothelial-to-haematopoietic transition at the single cell level identifies cell cycle regulation as a driver of differentiation. Genome Biol. 21, 157 (2020).
pubmed: 32611441 pmcid: 7329542 doi: 10.1186/s13059-020-02058-4
Pauklin, S. & Vallier, L. The cell-cycle state of stem cells determines cell fate propensity. Cell 155, 135–147 (2013).
pubmed: 24074866 pmcid: 3898746 doi: 10.1016/j.cell.2013.08.031
Burstyn-Cohen, T. & Kalcheim, C. Association between the cell cycle and neural crest delamination through specific regulation of G1/S transition. Dev. Cell 3, 383–395 (2002).
pubmed: 12361601 doi: 10.1016/S1534-5807(02)00221-6
Ko, C. S., Kalakuntla, P. & Martin, A. C. Apical constriction reversal upon mitotic entry underlies different morphogenetic outcomes of cell division. Mol. Biol. Cell 31, 1663–1674 (2020).
pubmed: 32129704 pmcid: 7521848 doi: 10.1091/mbc.E19-12-0673
Easterbrook, J. et al. Analysis of the spatiotemporal development of hematopoietic stem and progenitor cells in the early human embryo. Stem Cell Rep. https://doi.org/10.1016/j.stemcr.2019.03.003 (2019).
doi: 10.1016/j.stemcr.2019.03.003
Ivanovs, A. et al. Highly potent human hematopoietic stem cells first emerge in the intraembryonic aorta-gonad-mesonephros region. J. Exp. Med. 208, 2417–2427 (2011).
pubmed: 22042975 pmcid: 3256972 doi: 10.1084/jem.20111688
Dobin, A. et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics 29, 15–21 (2013).
pubmed: 23104886 doi: 10.1093/bioinformatics/bts635
Liao, Y., Smyth, G. K. & Shi, W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics 30, 923–930 (2014).
pubmed: 24227677 doi: 10.1093/bioinformatics/btt656
Love, M. I., Huber, W. & Anders, S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 15, 550 (2014).
pubmed: 25516281 pmcid: 4302049 doi: 10.1186/s13059-014-0550-8
Wu, T. et al. clusterProfiler 4.0: a universal enrichment tool for interpreting omics data. Innovation 2, 100141 (2021).
pubmed: 34557778 pmcid: 8454663
Bausch-Fluck, D. et al. The in silico human surfaceome. Proc. Natl Acad. Sci. USA 115, E10988–E10997 (2018).
pubmed: 30373828 pmcid: 6243280 doi: 10.1073/pnas.1808790115
Ditadi, A. & Sturgeon, C. M. Directed differentiation of definitive hemogenic endothelium and hematopoietic progenitors from human pluripotent stem cells. Methods 101, 65–72 (2016).
pubmed: 26439174 doi: 10.1016/j.ymeth.2015.10.001
Stuart, T. et al. Comprehensive integration of single-cell data. Cell 177, 1888–1902.e21 (2019).
pubmed: 31178118 pmcid: 6687398 doi: 10.1016/j.cell.2019.05.031
McInnes, L., Healy, J., Saul, N. & Großberger, L. UMAP: Uniform Manifold Approximation and Projection. J. Open Source Softw. 3, 861 (2018).
doi: 10.21105/joss.00861
Qiu, X. et al. Reversed graph embedding resolves complex single-cell trajectories. Nat. Methods 14, 979–982 (2017).
pubmed: 28825705 pmcid: 5764547 doi: 10.1038/nmeth.4402
Trapnell, C. et al. The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells. Nat. Biotechnol. 32, 381–386 (2014).
pubmed: 24658644 pmcid: 4122333 doi: 10.1038/nbt.2859
Wolf, F. A. et al. PAGA: graph abstraction reconciles clustering with trajectory inference through a topology preserving map of single cells. Genome Biol. 20, 59 (2019).
pubmed: 30890159 pmcid: 6425583 doi: 10.1186/s13059-019-1663-x
Wolf, F. A., Angerer, P. & Theis, F. J. SCANPY: large-scale single-cell gene expression data analysis. Genome Biol. 19, 15 (2018).
pubmed: 29409532 pmcid: 5802054 doi: 10.1186/s13059-017-1382-0
Shao, X. et al. CellTalkDB: a manually curated database of ligand–receptor interactions in humans and mice. Brief. Bioinform. 22, bbaa269 (2020).
doi: 10.1093/bib/bbaa269
Thomson, J. A. et al. Embryonic stem cell lines derived from human blastocysts. Science 282, 1145–1147 (1998).
pubmed: 9804556 doi: 10.1126/science.282.5391.1145
Mohtashami, M. et al. Direct comparison of Dll1- and Dll4-mediated Notch activation levels shows differential lymphomyeloid lineage commitment outcomes. J. Immunol. 185, 867–876 (2010).
pubmed: 20548034 doi: 10.4049/jimmunol.1000782
Montel-Hagen, A. et al. Organoid-induced differentiation of conventional T cells from human pluripotent stem cells. Cell Stem Cell https://doi.org/10.1016/j.stem.2018.12.011 (2019).
doi: 10.1016/j.stem.2018.12.011 pubmed: 30661959 pmcid: 6687310
Dolens, A. et al. Distinct Notch1 and BCL11B requirements mediate human γδ/αβ T cell development. EMBO Rep. 21, e49006 (2020).
pubmed: 32255245 pmcid: 7202205 doi: 10.15252/embr.201949006
Kennedy, M. et al. T lymphocyte potential marks the emergence of definitive hematopoietic progenitors in human pluripotent stem cell differentiation cultures. Cell Rep. 2, 1722–1735 (2012).
pubmed: 23219550 doi: 10.1016/j.celrep.2012.11.003
Scarfò, R. et al. Data for “CD32 captures committed haemogenic endothelial cells during human embryonic development.”. San. Raffaele Open Res. Data Repos. https://doi.org/10.17632/ds6rcgfp7y.1 (2024).
doi: 10.17632/ds6rcgfp7y.1
Scarfo. HEC2023 GitLab http://www.bioinfotiget.it/gitlab/custom/Scarfo_HEC2023 (2023).

Auteurs

Rebecca Scarfò (R)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Lauren N Randolph (LN)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Monah Abou Alezz (M)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Mahassen El Khoury (M)

Université de Strasbourg, Inserm, IRFAC/UMR-S1113, FHU ARRIMAGE, FMTS, Strasbourg, France.

Amélie Gersch (A)

Université de Strasbourg, Inserm, IRFAC/UMR-S1113, FHU ARRIMAGE, FMTS, Strasbourg, France.

Zhong-Yin Li (ZY)

Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Stephanie A Luff (SA)

Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Andrea Tavosanis (A)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Giulia Ferrari Ramondo (G)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Sara Valsoni (S)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Sara Cascione (S)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Emma Didelon (E)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Laura Passerini (L)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Giada Amodio (G)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Chiara Brandas (C)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Anna Villa (A)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Institute of Genetic and Biomedical Research, Milan Unit, National Research Council, Milan, Italy.

Silvia Gregori (S)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Ivan Merelli (I)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Institute for Biomedical Technologies, National Research Council, Milan, Italy.

Jean-Noël Freund (JN)

Université de Strasbourg, Inserm, IRFAC/UMR-S1113, FHU ARRIMAGE, FMTS, Strasbourg, France.
INSERM U1256-NGERE, Université de Lorraine, Vandoeuvre-lès-Nancy, France.

Christopher M Sturgeon (CM)

Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Manuela Tavian (M)

Université de Strasbourg, Inserm, IRFAC/UMR-S1113, FHU ARRIMAGE, FMTS, Strasbourg, France. manuela.tavian@inserm.fr.

Andrea Ditadi (A)

San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy. ditadi.andrea@hsr.it.

Classifications MeSH