Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow
The progenitor stage of commitment toward the conventional dendritic cell subsets and the transcriptional networks that control it remain poorly understood. Two articles from Ginhoux and colleagues and Murphy and colleagues offer insight into these processes. Mouse conventional dendritic cells (cDCs...
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Veröffentlicht in: | Nature immunology 2015-07, Vol.16 (7), p.718-728 |
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creator | Schlitzer, Andreas Sivakamasundari, V Chen, Jinmiao Sumatoh, Hermi Rizal Bin Schreuder, Jaring Lum, Josephine Malleret, Benoit Zhang, Sanqian Larbi, Anis Zolezzi, Francesca Renia, Laurent Poidinger, Michael Naik, Shalin Newell, Evan W Robson, Paul Ginhoux, Florent |
description | The progenitor stage of commitment toward the conventional dendritic cell subsets and the transcriptional networks that control it remain poorly understood. Two articles from Ginhoux and colleagues and Murphy and colleagues offer insight into these processes.
Mouse conventional dendritic cells (cDCs) can be classified into two functionally distinct lineages: the CD8α
+
(CD103
+
) cDC1 lineage, and the CD11b
+
cDC2 lineage. cDCs arise from a cascade of bone marrow (BM) DC-committed progenitor cells that include the common DC progenitors (CDPs) and pre-DCs, which exit the BM and seed peripheral tissues before differentiating locally into mature cDCs. Where and when commitment to the cDC1 or cDC2 lineage occurs remains poorly understood. Here we found that transcriptional signatures of the cDC1 and cDC2 lineages became evident at the single-cell level from the CDP stage. We also identified Siglec-H and Ly6C as lineage markers that distinguished pre-DC subpopulations committed to the cDC1 lineage (Siglec-H
−
Ly6C
−
pre-DCs) or cDC2 lineage (Siglec-H
−
Ly6C
+
pre-DCs). Our results indicate that commitment to the cDC1 or cDC2 lineage occurs in the BM and not in the periphery. |
doi_str_mv | 10.1038/ni.3200 |
format | Article |
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Mouse conventional dendritic cells (cDCs) can be classified into two functionally distinct lineages: the CD8α
+
(CD103
+
) cDC1 lineage, and the CD11b
+
cDC2 lineage. cDCs arise from a cascade of bone marrow (BM) DC-committed progenitor cells that include the common DC progenitors (CDPs) and pre-DCs, which exit the BM and seed peripheral tissues before differentiating locally into mature cDCs. Where and when commitment to the cDC1 or cDC2 lineage occurs remains poorly understood. Here we found that transcriptional signatures of the cDC1 and cDC2 lineages became evident at the single-cell level from the CDP stage. We also identified Siglec-H and Ly6C as lineage markers that distinguished pre-DC subpopulations committed to the cDC1 lineage (Siglec-H
−
Ly6C
−
pre-DCs) or cDC2 lineage (Siglec-H
−
Ly6C
+
pre-DCs). Our results indicate that commitment to the cDC1 or cDC2 lineage occurs in the BM and not in the periphery.</description><identifier>ISSN: 1529-2908</identifier><identifier>EISSN: 1529-2916</identifier><identifier>DOI: 10.1038/ni.3200</identifier><identifier>PMID: 26054720</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>13 ; 13/31 ; 38/39 ; 38/91 ; 631/250/2504/133/2505 ; Animals ; Antigens, CD - immunology ; Antigens, CD - metabolism ; Antigens, Ly - genetics ; Antigens, Ly - immunology ; Antigens, Ly - metabolism ; Biomedicine ; Bone marrow ; Bone Marrow Cells - immunology ; Bone Marrow Cells - metabolism ; CD11b Antigen - immunology ; CD11b Antigen - metabolism ; CD8 Antigens - immunology ; CD8 Antigens - metabolism ; Cell development (Biology) ; Cell Lineage - genetics ; Cell Lineage - immunology ; Cells, Cultured ; Cluster Analysis ; Dendritic cells ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Dendritic Cells - ultrastructure ; Flow Cytometry ; Genetic aspects ; Immune response ; Immunology ; Infectious Diseases ; Integrin alpha Chains - immunology ; Integrin alpha Chains - metabolism ; Lectins - genetics ; Lectins - immunology ; Lectins - metabolism ; Medical research ; Medicine, Experimental ; Mice, Inbred C57BL ; Mice, Transgenic ; Microscopy, Electron, Scanning ; Oligonucleotide Array Sequence Analysis ; Properties ; Receptors, Cell Surface - genetics ; Receptors, Cell Surface - immunology ; Receptors, Cell Surface - metabolism ; Single-Cell Analysis - methods ; Stem Cells - immunology ; Stem Cells - metabolism ; Subpopulations ; Transcriptome - genetics ; Transcriptome - immunology</subject><ispartof>Nature immunology, 2015-07, Vol.16 (7), p.718-728</ispartof><rights>Springer Nature America, Inc. 2015</rights><rights>COPYRIGHT 2015 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jul 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-20234c99c98394f57a637f8351489e23f4d928d12fc4e5b9cb9a22e2c7bafca83</citedby><cites>FETCH-LOGICAL-c542t-20234c99c98394f57a637f8351489e23f4d928d12fc4e5b9cb9a22e2c7bafca83</cites><orcidid>0000-0001-7547-6423 ; 0000-0003-0349-1557 ; 0000-0002-1047-2277 ; 0000-0002-2857-7755 ; 0000-0002-0191-3958 ; 0000-0002-2889-243X ; 0000000210472277 ; 0000000175476423 ; 0000000201913958 ; 0000000303491557 ; 0000000228577755 ; 000000022889243X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ni.3200$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ni.3200$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26054720$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schlitzer, Andreas</creatorcontrib><creatorcontrib>Sivakamasundari, V</creatorcontrib><creatorcontrib>Chen, Jinmiao</creatorcontrib><creatorcontrib>Sumatoh, Hermi Rizal Bin</creatorcontrib><creatorcontrib>Schreuder, Jaring</creatorcontrib><creatorcontrib>Lum, Josephine</creatorcontrib><creatorcontrib>Malleret, Benoit</creatorcontrib><creatorcontrib>Zhang, Sanqian</creatorcontrib><creatorcontrib>Larbi, Anis</creatorcontrib><creatorcontrib>Zolezzi, Francesca</creatorcontrib><creatorcontrib>Renia, Laurent</creatorcontrib><creatorcontrib>Poidinger, Michael</creatorcontrib><creatorcontrib>Naik, Shalin</creatorcontrib><creatorcontrib>Newell, Evan W</creatorcontrib><creatorcontrib>Robson, Paul</creatorcontrib><creatorcontrib>Ginhoux, Florent</creatorcontrib><title>Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow</title><title>Nature immunology</title><addtitle>Nat Immunol</addtitle><addtitle>Nat Immunol</addtitle><description>The progenitor stage of commitment toward the conventional dendritic cell subsets and the transcriptional networks that control it remain poorly understood. Two articles from Ginhoux and colleagues and Murphy and colleagues offer insight into these processes.
Mouse conventional dendritic cells (cDCs) can be classified into two functionally distinct lineages: the CD8α
+
(CD103
+
) cDC1 lineage, and the CD11b
+
cDC2 lineage. cDCs arise from a cascade of bone marrow (BM) DC-committed progenitor cells that include the common DC progenitors (CDPs) and pre-DCs, which exit the BM and seed peripheral tissues before differentiating locally into mature cDCs. Where and when commitment to the cDC1 or cDC2 lineage occurs remains poorly understood. Here we found that transcriptional signatures of the cDC1 and cDC2 lineages became evident at the single-cell level from the CDP stage. We also identified Siglec-H and Ly6C as lineage markers that distinguished pre-DC subpopulations committed to the cDC1 lineage (Siglec-H
−
Ly6C
−
pre-DCs) or cDC2 lineage (Siglec-H
−
Ly6C
+
pre-DCs). Our results indicate that commitment to the cDC1 or cDC2 lineage occurs in the BM and not in the periphery.</description><subject>13</subject><subject>13/31</subject><subject>38/39</subject><subject>38/91</subject><subject>631/250/2504/133/2505</subject><subject>Animals</subject><subject>Antigens, CD - immunology</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, Ly - genetics</subject><subject>Antigens, Ly - immunology</subject><subject>Antigens, Ly - metabolism</subject><subject>Biomedicine</subject><subject>Bone marrow</subject><subject>Bone Marrow Cells - immunology</subject><subject>Bone Marrow Cells - metabolism</subject><subject>CD11b Antigen - immunology</subject><subject>CD11b Antigen - metabolism</subject><subject>CD8 Antigens - immunology</subject><subject>CD8 Antigens - metabolism</subject><subject>Cell development (Biology)</subject><subject>Cell Lineage - genetics</subject><subject>Cell Lineage - immunology</subject><subject>Cells, Cultured</subject><subject>Cluster Analysis</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Dendritic Cells - ultrastructure</subject><subject>Flow Cytometry</subject><subject>Genetic aspects</subject><subject>Immune response</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><subject>Integrin alpha Chains - immunology</subject><subject>Integrin alpha Chains - metabolism</subject><subject>Lectins - genetics</subject><subject>Lectins - immunology</subject><subject>Lectins - metabolism</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Microscopy, Electron, Scanning</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Properties</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - immunology</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Single-Cell Analysis - methods</subject><subject>Stem Cells - immunology</subject><subject>Stem Cells - metabolism</subject><subject>Subpopulations</subject><subject>Transcriptome - genetics</subject><subject>Transcriptome - immunology</subject><issn>1529-2908</issn><issn>1529-2916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkttuFSEUhidGY-vW-AaGxAv1YrbAMANcNrsedtLExMM1YZjFSDMDCozad_ChZWxt3Y0XhgtW4Pt_WIeqekzwluBGvPRu21CM71THpKWyppJ0d69jLI6qBymdY0wY79j96oh2uGWc4uPq534An511RmcXPAoWmdMdqZH2wxrR2oR5djnDgE536EsMI3iXQ0wowjfQU0Kg43SBJudBj1AINzs_Ip1R_gxoVRfbAylKeSWd_030wQOadYzh-8Pqni2O8Ohq31SfXr_6uHtbn717s9-dnNWmZTTXFNOGGSmNFI1ktuW6a7gVTUuYkEAbywZJxUCoNQzaXppeakqBGt5ra7RoNtXzS9_yp68LpKxmlwxMk_YQlqQI541oit9_oJ3ElGDOZUGf3kLPwxJ9SaQYdh2Xgon2hhr1BMp5G3LUZjVVJ6y0sMWivL6ptv-gyhpgdqZUzLpyfiB4cSAoTIYfedRLSmr_4f0h--ySNTGkFMGqtWk6XiiC1TpOyju1jlMhn1yltPQzDNfcn_m5KU8qV36E-FfOt7x-Afhizqs</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Schlitzer, Andreas</creator><creator>Sivakamasundari, V</creator><creator>Chen, Jinmiao</creator><creator>Sumatoh, Hermi Rizal Bin</creator><creator>Schreuder, Jaring</creator><creator>Lum, Josephine</creator><creator>Malleret, Benoit</creator><creator>Zhang, Sanqian</creator><creator>Larbi, Anis</creator><creator>Zolezzi, Francesca</creator><creator>Renia, Laurent</creator><creator>Poidinger, Michael</creator><creator>Naik, Shalin</creator><creator>Newell, Evan W</creator><creator>Robson, Paul</creator><creator>Ginhoux, Florent</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><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>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7547-6423</orcidid><orcidid>https://orcid.org/0000-0003-0349-1557</orcidid><orcidid>https://orcid.org/0000-0002-1047-2277</orcidid><orcidid>https://orcid.org/0000-0002-2857-7755</orcidid><orcidid>https://orcid.org/0000-0002-0191-3958</orcidid><orcidid>https://orcid.org/0000-0002-2889-243X</orcidid><orcidid>https://orcid.org/0000000210472277</orcidid><orcidid>https://orcid.org/0000000175476423</orcidid><orcidid>https://orcid.org/0000000201913958</orcidid><orcidid>https://orcid.org/0000000303491557</orcidid><orcidid>https://orcid.org/0000000228577755</orcidid><orcidid>https://orcid.org/000000022889243X</orcidid></search><sort><creationdate>20150701</creationdate><title>Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow</title><author>Schlitzer, Andreas ; Sivakamasundari, V ; Chen, Jinmiao ; Sumatoh, Hermi Rizal Bin ; Schreuder, Jaring ; Lum, Josephine ; Malleret, Benoit ; Zhang, Sanqian ; Larbi, Anis ; Zolezzi, Francesca ; Renia, Laurent ; Poidinger, Michael ; Naik, Shalin ; Newell, Evan W ; Robson, Paul ; Ginhoux, Florent</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-20234c99c98394f57a637f8351489e23f4d928d12fc4e5b9cb9a22e2c7bafca83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>13</topic><topic>13/31</topic><topic>38/39</topic><topic>38/91</topic><topic>631/250/2504/133/2505</topic><topic>Animals</topic><topic>Antigens, CD - immunology</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, Ly - genetics</topic><topic>Antigens, Ly - immunology</topic><topic>Antigens, Ly - metabolism</topic><topic>Biomedicine</topic><topic>Bone marrow</topic><topic>Bone Marrow Cells - immunology</topic><topic>Bone Marrow Cells - metabolism</topic><topic>CD11b Antigen - immunology</topic><topic>CD11b Antigen - metabolism</topic><topic>CD8 Antigens - immunology</topic><topic>CD8 Antigens - metabolism</topic><topic>Cell development (Biology)</topic><topic>Cell Lineage - genetics</topic><topic>Cell Lineage - immunology</topic><topic>Cells, Cultured</topic><topic>Cluster Analysis</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Dendritic Cells - ultrastructure</topic><topic>Flow Cytometry</topic><topic>Genetic aspects</topic><topic>Immune response</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><topic>Integrin alpha Chains - immunology</topic><topic>Integrin alpha Chains - metabolism</topic><topic>Lectins - genetics</topic><topic>Lectins - immunology</topic><topic>Lectins - metabolism</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Microscopy, Electron, Scanning</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Properties</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Cell Surface - immunology</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Single-Cell Analysis - methods</topic><topic>Stem Cells - immunology</topic><topic>Stem Cells - metabolism</topic><topic>Subpopulations</topic><topic>Transcriptome - genetics</topic><topic>Transcriptome - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schlitzer, Andreas</creatorcontrib><creatorcontrib>Sivakamasundari, V</creatorcontrib><creatorcontrib>Chen, Jinmiao</creatorcontrib><creatorcontrib>Sumatoh, Hermi Rizal Bin</creatorcontrib><creatorcontrib>Schreuder, Jaring</creatorcontrib><creatorcontrib>Lum, Josephine</creatorcontrib><creatorcontrib>Malleret, Benoit</creatorcontrib><creatorcontrib>Zhang, Sanqian</creatorcontrib><creatorcontrib>Larbi, Anis</creatorcontrib><creatorcontrib>Zolezzi, Francesca</creatorcontrib><creatorcontrib>Renia, Laurent</creatorcontrib><creatorcontrib>Poidinger, Michael</creatorcontrib><creatorcontrib>Naik, Shalin</creatorcontrib><creatorcontrib>Newell, Evan W</creatorcontrib><creatorcontrib>Robson, Paul</creatorcontrib><creatorcontrib>Ginhoux, Florent</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schlitzer, Andreas</au><au>Sivakamasundari, V</au><au>Chen, Jinmiao</au><au>Sumatoh, Hermi Rizal Bin</au><au>Schreuder, Jaring</au><au>Lum, Josephine</au><au>Malleret, Benoit</au><au>Zhang, Sanqian</au><au>Larbi, Anis</au><au>Zolezzi, Francesca</au><au>Renia, Laurent</au><au>Poidinger, Michael</au><au>Naik, Shalin</au><au>Newell, Evan W</au><au>Robson, Paul</au><au>Ginhoux, Florent</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow</atitle><jtitle>Nature immunology</jtitle><stitle>Nat Immunol</stitle><addtitle>Nat Immunol</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>16</volume><issue>7</issue><spage>718</spage><epage>728</epage><pages>718-728</pages><issn>1529-2908</issn><eissn>1529-2916</eissn><abstract>The progenitor stage of commitment toward the conventional dendritic cell subsets and the transcriptional networks that control it remain poorly understood. Two articles from Ginhoux and colleagues and Murphy and colleagues offer insight into these processes.
Mouse conventional dendritic cells (cDCs) can be classified into two functionally distinct lineages: the CD8α
+
(CD103
+
) cDC1 lineage, and the CD11b
+
cDC2 lineage. cDCs arise from a cascade of bone marrow (BM) DC-committed progenitor cells that include the common DC progenitors (CDPs) and pre-DCs, which exit the BM and seed peripheral tissues before differentiating locally into mature cDCs. Where and when commitment to the cDC1 or cDC2 lineage occurs remains poorly understood. Here we found that transcriptional signatures of the cDC1 and cDC2 lineages became evident at the single-cell level from the CDP stage. We also identified Siglec-H and Ly6C as lineage markers that distinguished pre-DC subpopulations committed to the cDC1 lineage (Siglec-H
−
Ly6C
−
pre-DCs) or cDC2 lineage (Siglec-H
−
Ly6C
+
pre-DCs). Our results indicate that commitment to the cDC1 or cDC2 lineage occurs in the BM and not in the periphery.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>26054720</pmid><doi>10.1038/ni.3200</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7547-6423</orcidid><orcidid>https://orcid.org/0000-0003-0349-1557</orcidid><orcidid>https://orcid.org/0000-0002-1047-2277</orcidid><orcidid>https://orcid.org/0000-0002-2857-7755</orcidid><orcidid>https://orcid.org/0000-0002-0191-3958</orcidid><orcidid>https://orcid.org/0000-0002-2889-243X</orcidid><orcidid>https://orcid.org/0000000210472277</orcidid><orcidid>https://orcid.org/0000000175476423</orcidid><orcidid>https://orcid.org/0000000201913958</orcidid><orcidid>https://orcid.org/0000000303491557</orcidid><orcidid>https://orcid.org/0000000228577755</orcidid><orcidid>https://orcid.org/000000022889243X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1529-2908 |
ispartof | Nature immunology, 2015-07, Vol.16 (7), p.718-728 |
issn | 1529-2908 1529-2916 |
language | eng |
recordid | cdi_proquest_miscellaneous_1773833518 |
source | MEDLINE; Springer Nature - Complete Springer Journals; Nature Journals Online |
subjects | 13 13/31 38/39 38/91 631/250/2504/133/2505 Animals Antigens, CD - immunology Antigens, CD - metabolism Antigens, Ly - genetics Antigens, Ly - immunology Antigens, Ly - metabolism Biomedicine Bone marrow Bone Marrow Cells - immunology Bone Marrow Cells - metabolism CD11b Antigen - immunology CD11b Antigen - metabolism CD8 Antigens - immunology CD8 Antigens - metabolism Cell development (Biology) Cell Lineage - genetics Cell Lineage - immunology Cells, Cultured Cluster Analysis Dendritic cells Dendritic Cells - immunology Dendritic Cells - metabolism Dendritic Cells - ultrastructure Flow Cytometry Genetic aspects Immune response Immunology Infectious Diseases Integrin alpha Chains - immunology Integrin alpha Chains - metabolism Lectins - genetics Lectins - immunology Lectins - metabolism Medical research Medicine, Experimental Mice, Inbred C57BL Mice, Transgenic Microscopy, Electron, Scanning Oligonucleotide Array Sequence Analysis Properties Receptors, Cell Surface - genetics Receptors, Cell Surface - immunology Receptors, Cell Surface - metabolism Single-Cell Analysis - methods Stem Cells - immunology Stem Cells - metabolism Subpopulations Transcriptome - genetics Transcriptome - immunology |
title | Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow |
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