Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs

Human lymphopoiesis is a dynamic lifelong process that starts in utero 6 weeks postconception. Although fetal B-lymphopoiesis remains poorly defined, it is key to understanding leukemia initiation in early life. Here, we provide a comprehensive analysis of the human fetal B-cell developmental hierar...

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Veröffentlicht in:Blood 2019-09, Vol.134 (13), p.1059-1071
Hauptverfasser: O'Byrne, Sorcha, Elliott, Natalina, Rice, Siobhan, Buck, Gemma, Fordham, Nicholas, Garnett, Catherine, Godfrey, Laura, Crump, Nicholas T., Wright, Gary, Inglott, Sarah, Hua, Peng, Psaila, Bethan, Povinelli, Benjamin, Knapp, David J.H.F., Agraz-Doblas, Antonio, Bueno, Clara, Varela, Ignacio, Bennett, Phillip, Koohy, Hashem, Watt, Suzanne M., Karadimitris, Anastasios, Mead, Adam J., Ancliff, Phillip, Vyas, Paresh, Menendez, Pablo, Milne, Thomas A., Roberts, Irene, Roy, Anindita
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container_end_page 1071
container_issue 13
container_start_page 1059
container_title Blood
container_volume 134
creator O'Byrne, Sorcha
Elliott, Natalina
Rice, Siobhan
Buck, Gemma
Fordham, Nicholas
Garnett, Catherine
Godfrey, Laura
Crump, Nicholas T.
Wright, Gary
Inglott, Sarah
Hua, Peng
Psaila, Bethan
Povinelli, Benjamin
Knapp, David J.H.F.
Agraz-Doblas, Antonio
Bueno, Clara
Varela, Ignacio
Bennett, Phillip
Koohy, Hashem
Watt, Suzanne M.
Karadimitris, Anastasios
Mead, Adam J.
Ancliff, Phillip
Vyas, Paresh
Menendez, Pablo
Milne, Thomas A.
Roberts, Irene
Roy, Anindita
description Human lymphopoiesis is a dynamic lifelong process that starts in utero 6 weeks postconception. Although fetal B-lymphopoiesis remains poorly defined, it is key to understanding leukemia initiation in early life. Here, we provide a comprehensive analysis of the human fetal B-cell developmental hierarchy. We report the presence in fetal tissues of 2 distinct CD19+ B-progenitors, an adult-type CD10+ve ProB-progenitor and a new CD10-ve PreProB-progenitor, and describe their molecular and functional characteristics. PreProB-progenitors and ProB-progenitors appear early in the first trimester in embryonic liver, followed by a sustained second wave of B-progenitor development in fetal bone marrow (BM), where together they form >40% of the total hematopoietic stem cell/progenitor pool. Almost one-third of fetal B-progenitors are CD10-ve PreProB-progenitors, whereas, by contrast, PreProB-progenitors are almost undetectable (0.53% ± 0.24%) in adult BM. Single-cell transcriptomics and functional assays place fetal PreProB-progenitors upstream of ProB-progenitors, identifying them as the first B-lymphoid–restricted progenitor in human fetal life. Although fetal BM PreProB-progenitors and ProB-progenitors both give rise solely to B-lineage cells, they are transcriptionally distinct. As with their fetal counterparts, adult BM PreProB-progenitors give rise only to B-lineage cells in vitro and express the expected B-lineage gene expression program. However, fetal PreProB-progenitors display a distinct, ontogeny-related gene expression pattern that is not seen in adult PreProB-progenitors, and they share transcriptomic signatures with CD10-ve B-progenitor infant acute lymphoblastic leukemia blast cells. These data identify PreProB-progenitors as the earliest B-lymphoid–restricted progenitor in human fetal life and suggest that this fetal-restricted committed B-progenitor might provide a permissive cellular context for prenatal B-progenitor leukemia initiation. •CD10-ve PreProB-progenitors are the earliest fetal B-lymphoid–restricted progenitors and are enriched in fetal BM.•Fetal PreProB-progenitors have a unique ontogeny-related developmental gene expression program distinct from their rare adult counterparts. [Display omitted]
doi_str_mv 10.1182/blood.2019001289
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Although fetal B-lymphopoiesis remains poorly defined, it is key to understanding leukemia initiation in early life. Here, we provide a comprehensive analysis of the human fetal B-cell developmental hierarchy. We report the presence in fetal tissues of 2 distinct CD19+ B-progenitors, an adult-type CD10+ve ProB-progenitor and a new CD10-ve PreProB-progenitor, and describe their molecular and functional characteristics. PreProB-progenitors and ProB-progenitors appear early in the first trimester in embryonic liver, followed by a sustained second wave of B-progenitor development in fetal bone marrow (BM), where together they form &gt;40% of the total hematopoietic stem cell/progenitor pool. Almost one-third of fetal B-progenitors are CD10-ve PreProB-progenitors, whereas, by contrast, PreProB-progenitors are almost undetectable (0.53% ± 0.24%) in adult BM. Single-cell transcriptomics and functional assays place fetal PreProB-progenitors upstream of ProB-progenitors, identifying them as the first B-lymphoid–restricted progenitor in human fetal life. Although fetal BM PreProB-progenitors and ProB-progenitors both give rise solely to B-lineage cells, they are transcriptionally distinct. As with their fetal counterparts, adult BM PreProB-progenitors give rise only to B-lineage cells in vitro and express the expected B-lineage gene expression program. However, fetal PreProB-progenitors display a distinct, ontogeny-related gene expression pattern that is not seen in adult PreProB-progenitors, and they share transcriptomic signatures with CD10-ve B-progenitor infant acute lymphoblastic leukemia blast cells. These data identify PreProB-progenitors as the earliest B-lymphoid–restricted progenitor in human fetal life and suggest that this fetal-restricted committed B-progenitor might provide a permissive cellular context for prenatal B-progenitor leukemia initiation. •CD10-ve PreProB-progenitors are the earliest fetal B-lymphoid–restricted progenitors and are enriched in fetal BM.•Fetal PreProB-progenitors have a unique ontogeny-related developmental gene expression program distinct from their rare adult counterparts. 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These data identify PreProB-progenitors as the earliest B-lymphoid–restricted progenitor in human fetal life and suggest that this fetal-restricted committed B-progenitor might provide a permissive cellular context for prenatal B-progenitor leukemia initiation. •CD10-ve PreProB-progenitors are the earliest fetal B-lymphoid–restricted progenitors and are enriched in fetal BM.•Fetal PreProB-progenitors have a unique ontogeny-related developmental gene expression program distinct from their rare adult counterparts. [Display omitted]</description><subject>Adult</subject><subject>Bone Marrow - embryology</subject><subject>Bone Marrow - metabolism</subject><subject>Cells, Cultured</subject><subject>Fetus - cytology</subject><subject>Fetus - embryology</subject><subject>Fetus - metabolism</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Humans</subject><subject>Liver - embryology</subject><subject>Liver - metabolism</subject><subject>Lymphopoiesis</subject><subject>Neprilysin - analysis</subject><subject>Neprilysin - genetics</subject><subject>Precursor Cells, B-Lymphoid - cytology</subject><subject>Precursor Cells, B-Lymphoid - metabolism</subject><subject>Transcriptome</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PHDEURa0oCBZCnypymWbIsz07H3RkFxIkJBpSWx77mTiasTe2Z9H-e7wskCqVm3PP872EfGZwwVjHvw1jCOaCA-sBGO_6D2TBlryrADh8JAsAaKq6b9kJOU3pT2FqwZfH5EQw0YlG9AvytHZJhy3GHQ2WKrpaM6g8Pqrstki_V5sYHtG7HCJ1nv6eJ-WpxaxGOjqL1Bn02VmHic7e_Z2RBp_3iV0VcVQZDTW4xTFspgKW1N4X1ZQ-kSOrxoTnr-8Z-XVz_bD6Wd3d_7hdXd1Vul52uRoMU7XSwjCNhqGxjbJ8aBvGW9W0ttc9t4NoFWvrYWjtUoECNpRyPWoLIMQZ-XrwlsPleynLqRTGcVQew5wk503X17zuoKBwQHUMKUW0chPdpOJOMpD7ueXL3PLf3CXy5dU-DxOa98DbvgW4PABYOm4dRpm0Q1_KuIg6SxPc_-3P2DuSIQ</recordid><startdate>20190926</startdate><enddate>20190926</enddate><creator>O'Byrne, Sorcha</creator><creator>Elliott, Natalina</creator><creator>Rice, Siobhan</creator><creator>Buck, Gemma</creator><creator>Fordham, Nicholas</creator><creator>Garnett, Catherine</creator><creator>Godfrey, Laura</creator><creator>Crump, Nicholas T.</creator><creator>Wright, Gary</creator><creator>Inglott, Sarah</creator><creator>Hua, Peng</creator><creator>Psaila, Bethan</creator><creator>Povinelli, Benjamin</creator><creator>Knapp, David J.H.F.</creator><creator>Agraz-Doblas, Antonio</creator><creator>Bueno, Clara</creator><creator>Varela, Ignacio</creator><creator>Bennett, Phillip</creator><creator>Koohy, Hashem</creator><creator>Watt, Suzanne M.</creator><creator>Karadimitris, Anastasios</creator><creator>Mead, Adam J.</creator><creator>Ancliff, Phillip</creator><creator>Vyas, Paresh</creator><creator>Menendez, Pablo</creator><creator>Milne, Thomas A.</creator><creator>Roberts, Irene</creator><creator>Roy, Anindita</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0413-4271</orcidid><orcidid>https://orcid.org/0000-0003-3931-0914</orcidid><orcidid>https://orcid.org/0000-0001-8607-5748</orcidid><orcidid>https://orcid.org/0000-0003-3774-5033</orcidid><orcidid>https://orcid.org/0000-0001-8198-9663</orcidid><orcidid>https://orcid.org/0000-0002-2161-9959</orcidid><orcidid>https://orcid.org/0000-0001-9610-6763</orcidid><orcidid>https://orcid.org/0000-0002-3116-1646</orcidid></search><sort><creationdate>20190926</creationdate><title>Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs</title><author>O'Byrne, Sorcha ; Elliott, Natalina ; Rice, Siobhan ; Buck, Gemma ; Fordham, Nicholas ; Garnett, Catherine ; Godfrey, Laura ; Crump, Nicholas T. ; Wright, Gary ; Inglott, Sarah ; Hua, Peng ; Psaila, Bethan ; Povinelli, Benjamin ; Knapp, David J.H.F. ; Agraz-Doblas, Antonio ; Bueno, Clara ; Varela, Ignacio ; Bennett, Phillip ; Koohy, Hashem ; Watt, Suzanne M. ; Karadimitris, Anastasios ; Mead, Adam J. ; Ancliff, Phillip ; Vyas, Paresh ; Menendez, Pablo ; Milne, Thomas A. ; Roberts, Irene ; Roy, Anindita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-bd1a4ac3d1ced1edf6af2b76127a67f9c92fb37a174bb7f5a0a01b3839ecf0033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Bone Marrow - embryology</topic><topic>Bone Marrow - metabolism</topic><topic>Cells, Cultured</topic><topic>Fetus - cytology</topic><topic>Fetus - embryology</topic><topic>Fetus - metabolism</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Humans</topic><topic>Liver - embryology</topic><topic>Liver - metabolism</topic><topic>Lymphopoiesis</topic><topic>Neprilysin - analysis</topic><topic>Neprilysin - genetics</topic><topic>Precursor Cells, B-Lymphoid - cytology</topic><topic>Precursor Cells, B-Lymphoid - metabolism</topic><topic>Transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Byrne, Sorcha</creatorcontrib><creatorcontrib>Elliott, Natalina</creatorcontrib><creatorcontrib>Rice, Siobhan</creatorcontrib><creatorcontrib>Buck, Gemma</creatorcontrib><creatorcontrib>Fordham, Nicholas</creatorcontrib><creatorcontrib>Garnett, Catherine</creatorcontrib><creatorcontrib>Godfrey, Laura</creatorcontrib><creatorcontrib>Crump, Nicholas T.</creatorcontrib><creatorcontrib>Wright, Gary</creatorcontrib><creatorcontrib>Inglott, Sarah</creatorcontrib><creatorcontrib>Hua, Peng</creatorcontrib><creatorcontrib>Psaila, Bethan</creatorcontrib><creatorcontrib>Povinelli, Benjamin</creatorcontrib><creatorcontrib>Knapp, David J.H.F.</creatorcontrib><creatorcontrib>Agraz-Doblas, Antonio</creatorcontrib><creatorcontrib>Bueno, Clara</creatorcontrib><creatorcontrib>Varela, Ignacio</creatorcontrib><creatorcontrib>Bennett, Phillip</creatorcontrib><creatorcontrib>Koohy, Hashem</creatorcontrib><creatorcontrib>Watt, Suzanne M.</creatorcontrib><creatorcontrib>Karadimitris, Anastasios</creatorcontrib><creatorcontrib>Mead, Adam J.</creatorcontrib><creatorcontrib>Ancliff, Phillip</creatorcontrib><creatorcontrib>Vyas, Paresh</creatorcontrib><creatorcontrib>Menendez, Pablo</creatorcontrib><creatorcontrib>Milne, Thomas A.</creatorcontrib><creatorcontrib>Roberts, Irene</creatorcontrib><creatorcontrib>Roy, Anindita</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Byrne, Sorcha</au><au>Elliott, Natalina</au><au>Rice, Siobhan</au><au>Buck, Gemma</au><au>Fordham, Nicholas</au><au>Garnett, Catherine</au><au>Godfrey, Laura</au><au>Crump, Nicholas T.</au><au>Wright, Gary</au><au>Inglott, Sarah</au><au>Hua, Peng</au><au>Psaila, Bethan</au><au>Povinelli, Benjamin</au><au>Knapp, David J.H.F.</au><au>Agraz-Doblas, Antonio</au><au>Bueno, Clara</au><au>Varela, Ignacio</au><au>Bennett, Phillip</au><au>Koohy, Hashem</au><au>Watt, Suzanne M.</au><au>Karadimitris, Anastasios</au><au>Mead, Adam J.</au><au>Ancliff, Phillip</au><au>Vyas, Paresh</au><au>Menendez, Pablo</au><au>Milne, Thomas A.</au><au>Roberts, Irene</au><au>Roy, Anindita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2019-09-26</date><risdate>2019</risdate><volume>134</volume><issue>13</issue><spage>1059</spage><epage>1071</epage><pages>1059-1071</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Human lymphopoiesis is a dynamic lifelong process that starts in utero 6 weeks postconception. Although fetal B-lymphopoiesis remains poorly defined, it is key to understanding leukemia initiation in early life. Here, we provide a comprehensive analysis of the human fetal B-cell developmental hierarchy. We report the presence in fetal tissues of 2 distinct CD19+ B-progenitors, an adult-type CD10+ve ProB-progenitor and a new CD10-ve PreProB-progenitor, and describe their molecular and functional characteristics. PreProB-progenitors and ProB-progenitors appear early in the first trimester in embryonic liver, followed by a sustained second wave of B-progenitor development in fetal bone marrow (BM), where together they form &gt;40% of the total hematopoietic stem cell/progenitor pool. Almost one-third of fetal B-progenitors are CD10-ve PreProB-progenitors, whereas, by contrast, PreProB-progenitors are almost undetectable (0.53% ± 0.24%) in adult BM. Single-cell transcriptomics and functional assays place fetal PreProB-progenitors upstream of ProB-progenitors, identifying them as the first B-lymphoid–restricted progenitor in human fetal life. Although fetal BM PreProB-progenitors and ProB-progenitors both give rise solely to B-lineage cells, they are transcriptionally distinct. As with their fetal counterparts, adult BM PreProB-progenitors give rise only to B-lineage cells in vitro and express the expected B-lineage gene expression program. However, fetal PreProB-progenitors display a distinct, ontogeny-related gene expression pattern that is not seen in adult PreProB-progenitors, and they share transcriptomic signatures with CD10-ve B-progenitor infant acute lymphoblastic leukemia blast cells. These data identify PreProB-progenitors as the earliest B-lymphoid–restricted progenitor in human fetal life and suggest that this fetal-restricted committed B-progenitor might provide a permissive cellular context for prenatal B-progenitor leukemia initiation. •CD10-ve PreProB-progenitors are the earliest fetal B-lymphoid–restricted progenitors and are enriched in fetal BM.•Fetal PreProB-progenitors have a unique ontogeny-related developmental gene expression program distinct from their rare adult counterparts. 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fulltext fulltext
identifier ISSN: 0006-4971
ispartof Blood, 2019-09, Vol.134 (13), p.1059-1071
issn 0006-4971
1528-0020
language eng
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source MEDLINE; Alma/SFX Local Collection; EZB Electronic Journals Library
subjects Adult
Bone Marrow - embryology
Bone Marrow - metabolism
Cells, Cultured
Fetus - cytology
Fetus - embryology
Fetus - metabolism
Gene Expression Regulation, Developmental
Humans
Liver - embryology
Liver - metabolism
Lymphopoiesis
Neprilysin - analysis
Neprilysin - genetics
Precursor Cells, B-Lymphoid - cytology
Precursor Cells, B-Lymphoid - metabolism
Transcriptome
title Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs
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