Production of the plasma-cell survival factor a proliferation-inducing ligand (APRIL) peaks in myeloid precursor cells from human bone marrow
The bone marrow (BM) is an organ extremely efficient in mediating long-term survival of plasma cells (PCs), ensuring an immune humoral memory. This implies that the BM must provide continuously key PC survival factors. Our results show that the BM is an organ constitutively rich in a proliferation-i...
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Veröffentlicht in: | Blood 2011-08, Vol.118 (7), p.1838-1844 |
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description | The bone marrow (BM) is an organ extremely efficient in mediating long-term survival of plasma cells (PCs), ensuring an immune humoral memory. This implies that the BM must provide continuously key PC survival factors. Our results show that the BM is an organ constitutively rich in a proliferation-inducing ligand (APRIL), a member of the tumor necrosis factor superfamily implicated in PC survival. APRIL production is induced during hematopoiesis in myeloid cells by non–lineage-committing factors such as stem cell factor, thrombopoietin, IL-3, and FMS-like tyrosine kinase 3 ligand. Notably, APRIL production, both in the human and mouse systems, peaks in myeloid precursor cells, before dropping in fully mature granulocytes. Myeloid cells secrete APRIL that circulates freely in BM plasma to act on PCs, usually at distance from APRIL production sites. Selective APRIL in vivo antagonism and in vitro coculture experiments further demonstrated that myeloid precursor cells mediates PC survival in an APRIL-dependent manner Thus, APRIL production by myeloid precursor cells shows that the 2 main BM functions, hematopoiesis and long-term PC survival, are linked. Such constitutive and high APRIL production may explain why BM mediates long-term PC survival. |
doi_str_mv | 10.1182/blood-2011-01-332940 |
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This implies that the BM must provide continuously key PC survival factors. Our results show that the BM is an organ constitutively rich in a proliferation-inducing ligand (APRIL), a member of the tumor necrosis factor superfamily implicated in PC survival. APRIL production is induced during hematopoiesis in myeloid cells by non–lineage-committing factors such as stem cell factor, thrombopoietin, IL-3, and FMS-like tyrosine kinase 3 ligand. Notably, APRIL production, both in the human and mouse systems, peaks in myeloid precursor cells, before dropping in fully mature granulocytes. Myeloid cells secrete APRIL that circulates freely in BM plasma to act on PCs, usually at distance from APRIL production sites. Selective APRIL in vivo antagonism and in vitro coculture experiments further demonstrated that myeloid precursor cells mediates PC survival in an APRIL-dependent manner Thus, APRIL production by myeloid precursor cells shows that the 2 main BM functions, hematopoiesis and long-term PC survival, are linked. Such constitutive and high APRIL production may explain why BM mediates long-term PC survival.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2011-01-332940</identifier><identifier>PMID: 21642598</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Bone Marrow Cells - cytology ; Bone Marrow Cells - metabolism ; Cell Survival ; Cells, Cultured ; Gene Knockout Techniques ; Hematologic and hematopoietic diseases ; Humans ; Leukopoiesis ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Myeloid Cells - cytology ; Myeloid Cells - metabolism ; Plasma Cells - cytology ; Plasma Cells - metabolism ; Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics ; Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism</subject><ispartof>Blood, 2011-08, Vol.118 (7), p.1838-1844</ispartof><rights>2011 American Society of Hematology</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-3595dde0f1098d1a8a9faa2956d45f7959ce209fab570ff8c61b1a486de77d583</citedby><cites>FETCH-LOGICAL-c503t-3595dde0f1098d1a8a9faa2956d45f7959ce209fab570ff8c61b1a486de77d583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24454482$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21642598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matthes, Thomas</creatorcontrib><creatorcontrib>Dunand-Sauthier, Isabelle</creatorcontrib><creatorcontrib>Santiago-Raber, Marie-Laure</creatorcontrib><creatorcontrib>Krause, Karl-Heinz</creatorcontrib><creatorcontrib>Donze, Olivier</creatorcontrib><creatorcontrib>Passweg, Jakob</creatorcontrib><creatorcontrib>McKee, Tomas</creatorcontrib><creatorcontrib>Huard, Bertrand</creatorcontrib><title>Production of the plasma-cell survival factor a proliferation-inducing ligand (APRIL) peaks in myeloid precursor cells from human bone marrow</title><title>Blood</title><addtitle>Blood</addtitle><description>The bone marrow (BM) is an organ extremely efficient in mediating long-term survival of plasma cells (PCs), ensuring an immune humoral memory. This implies that the BM must provide continuously key PC survival factors. Our results show that the BM is an organ constitutively rich in a proliferation-inducing ligand (APRIL), a member of the tumor necrosis factor superfamily implicated in PC survival. APRIL production is induced during hematopoiesis in myeloid cells by non–lineage-committing factors such as stem cell factor, thrombopoietin, IL-3, and FMS-like tyrosine kinase 3 ligand. Notably, APRIL production, both in the human and mouse systems, peaks in myeloid precursor cells, before dropping in fully mature granulocytes. Myeloid cells secrete APRIL that circulates freely in BM plasma to act on PCs, usually at distance from APRIL production sites. Selective APRIL in vivo antagonism and in vitro coculture experiments further demonstrated that myeloid precursor cells mediates PC survival in an APRIL-dependent manner Thus, APRIL production by myeloid precursor cells shows that the 2 main BM functions, hematopoiesis and long-term PC survival, are linked. Such constitutive and high APRIL production may explain why BM mediates long-term PC survival.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells - cytology</subject><subject>Bone Marrow Cells - metabolism</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>Gene Knockout Techniques</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Leukopoiesis</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Myeloid Cells - cytology</subject><subject>Myeloid Cells - metabolism</subject><subject>Plasma Cells - cytology</subject><subject>Plasma Cells - metabolism</subject><subject>Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics</subject><subject>Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9u1DAYxC0EotvCGyDkCwIOBtuxE-dSqaooVFqJCsHZ-uI_rcGJFztZ1IfgnXHYBW6cLFm_GY9nEHrG6BvGFH87xJQs4ZQxQhlpGt4L-gBtmOSKUMrpQ7ShlLZE9B07QaelfKWUiYbLx-iEs1Zw2asN-nmTk13MHNKEk8fzncO7CGUEYlyMuCx5H_YQsQczp4wB73KKwbsMq4SEqYrDdItjuIXJ4lcXN5-ut6_xzsG3gsOEx3sXU7BV5sySS7VYfQv2OY34bhlhwkOaHB4h5_TjCXrkIRb39HieoS9X7z5ffiDbj--vLy-2xEjazKSRvbTWUc9orywDBb0H4L1srZC-62VvHKf1bpAd9V6Zlg0MhGqt6zorVXOGXh5862--L67MegxlDQaTS0vRSgnBW9mxSooDaXIqJTuvdznUsPeaUb3uoH_voNcdNGX6sEOVPT8-sAyjs39Ff4qvwIsjAMVA9BkmE8o_TggphOKVOz9wrtaxDy7rYoKbjLOhNjprm8L_k_wCCoioyA</recordid><startdate>20110818</startdate><enddate>20110818</enddate><creator>Matthes, Thomas</creator><creator>Dunand-Sauthier, Isabelle</creator><creator>Santiago-Raber, Marie-Laure</creator><creator>Krause, Karl-Heinz</creator><creator>Donze, Olivier</creator><creator>Passweg, Jakob</creator><creator>McKee, Tomas</creator><creator>Huard, Bertrand</creator><general>Elsevier Inc</general><general>Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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></search><sort><creationdate>20110818</creationdate><title>Production of the plasma-cell survival factor a proliferation-inducing ligand (APRIL) peaks in myeloid precursor cells from human bone marrow</title><author>Matthes, Thomas ; Dunand-Sauthier, Isabelle ; Santiago-Raber, Marie-Laure ; Krause, Karl-Heinz ; Donze, Olivier ; Passweg, Jakob ; McKee, Tomas ; Huard, Bertrand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-3595dde0f1098d1a8a9faa2956d45f7959ce209fab570ff8c61b1a486de77d583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bone Marrow Cells - metabolism</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>Gene Knockout Techniques</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Leukopoiesis</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Myeloid Cells - cytology</topic><topic>Myeloid Cells - metabolism</topic><topic>Plasma Cells - cytology</topic><topic>Plasma Cells - metabolism</topic><topic>Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics</topic><topic>Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matthes, Thomas</creatorcontrib><creatorcontrib>Dunand-Sauthier, Isabelle</creatorcontrib><creatorcontrib>Santiago-Raber, Marie-Laure</creatorcontrib><creatorcontrib>Krause, Karl-Heinz</creatorcontrib><creatorcontrib>Donze, Olivier</creatorcontrib><creatorcontrib>Passweg, Jakob</creatorcontrib><creatorcontrib>McKee, Tomas</creatorcontrib><creatorcontrib>Huard, Bertrand</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</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>Matthes, Thomas</au><au>Dunand-Sauthier, Isabelle</au><au>Santiago-Raber, Marie-Laure</au><au>Krause, Karl-Heinz</au><au>Donze, Olivier</au><au>Passweg, Jakob</au><au>McKee, Tomas</au><au>Huard, Bertrand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Production of the plasma-cell survival factor a proliferation-inducing ligand (APRIL) peaks in myeloid precursor cells from human bone marrow</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2011-08-18</date><risdate>2011</risdate><volume>118</volume><issue>7</issue><spage>1838</spage><epage>1844</epage><pages>1838-1844</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>The bone marrow (BM) is an organ extremely efficient in mediating long-term survival of plasma cells (PCs), ensuring an immune humoral memory. This implies that the BM must provide continuously key PC survival factors. Our results show that the BM is an organ constitutively rich in a proliferation-inducing ligand (APRIL), a member of the tumor necrosis factor superfamily implicated in PC survival. APRIL production is induced during hematopoiesis in myeloid cells by non–lineage-committing factors such as stem cell factor, thrombopoietin, IL-3, and FMS-like tyrosine kinase 3 ligand. Notably, APRIL production, both in the human and mouse systems, peaks in myeloid precursor cells, before dropping in fully mature granulocytes. Myeloid cells secrete APRIL that circulates freely in BM plasma to act on PCs, usually at distance from APRIL production sites. Selective APRIL in vivo antagonism and in vitro coculture experiments further demonstrated that myeloid precursor cells mediates PC survival in an APRIL-dependent manner Thus, APRIL production by myeloid precursor cells shows that the 2 main BM functions, hematopoiesis and long-term PC survival, are linked. Such constitutive and high APRIL production may explain why BM mediates long-term PC survival.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>21642598</pmid><doi>10.1182/blood-2011-01-332940</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Bone Marrow Cells - cytology Bone Marrow Cells - metabolism Cell Survival Cells, Cultured Gene Knockout Techniques Hematologic and hematopoietic diseases Humans Leukopoiesis Medical sciences Mice Mice, Inbred C57BL Mice, Knockout Myeloid Cells - cytology Myeloid Cells - metabolism Plasma Cells - cytology Plasma Cells - metabolism Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics Tumor Necrosis Factor Ligand Superfamily Member 13 - metabolism |
title | Production of the plasma-cell survival factor a proliferation-inducing ligand (APRIL) peaks in myeloid precursor cells from human bone marrow |
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