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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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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•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><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.2019001289</identifier><identifier>PMID: 31383639</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Blood, 2019-09, Vol.134 (13), p.1059-1071</ispartof><rights>2019 American Society of Hematology</rights><rights>2019 by The American Society of Hematology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-bd1a4ac3d1ced1edf6af2b76127a67f9c92fb37a174bb7f5a0a01b3839ecf0033</citedby><cites>FETCH-LOGICAL-c458t-bd1a4ac3d1ced1edf6af2b76127a67f9c92fb37a174bb7f5a0a01b3839ecf0033</cites><orcidid>0000-0002-0413-4271 ; 0000-0003-3931-0914 ; 0000-0001-8607-5748 ; 0000-0003-3774-5033 ; 0000-0001-8198-9663 ; 0000-0002-2161-9959 ; 0000-0001-9610-6763 ; 0000-0002-3116-1646</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31383639$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs</title><title>Blood</title><addtitle>Blood</addtitle><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]</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 >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]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31383639</pmid><doi>10.1182/blood.2019001289</doi><tpages>13</tpages><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><oa>free_for_read</oa></addata></record> |
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ispartof | Blood, 2019-09, Vol.134 (13), p.1059-1071 |
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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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T09%3A11%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Discovery%20of%20a%20CD10-negative%20B-progenitor%20in%20human%20fetal%20life%20identifies%20unique%20ontogeny-related%20developmental%20programs&rft.jtitle=Blood&rft.au=O'Byrne,%20Sorcha&rft.date=2019-09-26&rft.volume=134&rft.issue=13&rft.spage=1059&rft.epage=1071&rft.pages=1059-1071&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood.2019001289&rft_dat=%3Cproquest_cross%3E2268942480%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2268942480&rft_id=info:pmid/31383639&rft_els_id=S0006497120707901&rfr_iscdi=true |