Pool Size of Pluripotential Hematopoietic Stem Cells Increased in Continuous Bone Marrow Culture by Friend Spleen Focus-Forming Virus
Continuous mouse bone marrow cultures were infected with Friend murine leukemia virus. Production of nonadherent (NA) and adherent cells, granulocyte-macrophage colony-forming unil(s) of progenitor cells (GM-CFUc), pluripotential hematopoietic stem cells (CFUs), the self-renewal potential (Rs) of CF...
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Veröffentlicht in: | JNCI : Journal of the National Cancer Institute 1983-02, Vol.70 (2), p.323-331 |
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creator | Greenberger, Joel S. Hottman, Nancy Lieberman, Miriam Botnick, LeslieE Sakakeeny, Mary Ann Eckner, Robert J. |
description | Continuous mouse bone marrow cultures were infected with Friend murine leukemia virus. Production of nonadherent (NA) and adherent cells, granulocyte-macrophage colony-forming unil(s) of progenitor cells (GM-CFUc), pluripotential hematopoietic stem cells (CFUs), the self-renewal potential (Rs) of CFUs, and generation of factor-dependent (FD) multipotenlial and committed permanent stem cell cloned lines were measured. Uninfected marrow cultures from C57BL/6J, C57BL/6JUt, B6.S, C3H/HeJ, (C57BL/6J × DBA/2J)F1, CD-1 Swiss, or N:NIH(S) mice generated NA cells, GM-CFUc, and CFUs for 20–41 weeks; cultures infected with Rauscher or other helper viruses generated them for 35–45 weeks. GM-CFUc and CFUs production in SFFV-positive cultures persisted for over 65 weeks and exceeded control levels by twentyfold to fiflyfold. The Rs of CFUs in SFFV-positive cultures was not detectably increased above control cultures. Multipotential (erythroid-neutrophil-mast cell-basophil-eosinophil) permanent FD cell clones were derived from control and SFFV-positive cultures. Thus SFFV amplifies the stem cell pool in vitro without detectably increasing the Rs capacity of CFUs. |
doi_str_mv | 10.1093/jnci/70.2.323 |
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Production of nonadherent (NA) and adherent cells, granulocyte-macrophage colony-forming unil(s) of progenitor cells (GM-CFUc), pluripotential hematopoietic stem cells (CFUs), the self-renewal potential (Rs) of CFUs, and generation of factor-dependent (FD) multipotenlial and committed permanent stem cell cloned lines were measured. Uninfected marrow cultures from C57BL/6J, C57BL/6JUt, B6.S, C3H/HeJ, (C57BL/6J × DBA/2J)F1, CD-1 Swiss, or N:NIH(S) mice generated NA cells, GM-CFUc, and CFUs for 20–41 weeks; cultures infected with Rauscher or other helper viruses generated them for 35–45 weeks. GM-CFUc and CFUs production in SFFV-positive cultures persisted for over 65 weeks and exceeded control levels by twentyfold to fiflyfold. The Rs of CFUs in SFFV-positive cultures was not detectably increased above control cultures. Multipotential (erythroid-neutrophil-mast cell-basophil-eosinophil) permanent FD cell clones were derived from control and SFFV-positive cultures. Thus SFFV amplifies the stem cell pool in vitro without detectably increasing the Rs capacity of CFUs.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/70.2.323</identifier><identifier>PMID: 6571939</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Animals ; Blood Cell Count ; Bone Marrow - microbiology ; Cell Line ; Friend murine leukemia virus - physiology ; Hematopoietic Stem Cells - microbiology ; Mice ; Mice, Inbred Strains ; Virus Replication</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1983-02, Vol.70 (2), p.323-331</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6571939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Greenberger, Joel S.</creatorcontrib><creatorcontrib>Hottman, Nancy</creatorcontrib><creatorcontrib>Lieberman, Miriam</creatorcontrib><creatorcontrib>Botnick, LeslieE</creatorcontrib><creatorcontrib>Sakakeeny, Mary Ann</creatorcontrib><creatorcontrib>Eckner, Robert J.</creatorcontrib><title>Pool Size of Pluripotential Hematopoietic Stem Cells Increased in Continuous Bone Marrow Culture by Friend Spleen Focus-Forming Virus</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>Continuous mouse bone marrow cultures were infected with Friend murine leukemia virus. Production of nonadherent (NA) and adherent cells, granulocyte-macrophage colony-forming unil(s) of progenitor cells (GM-CFUc), pluripotential hematopoietic stem cells (CFUs), the self-renewal potential (Rs) of CFUs, and generation of factor-dependent (FD) multipotenlial and committed permanent stem cell cloned lines were measured. Uninfected marrow cultures from C57BL/6J, C57BL/6JUt, B6.S, C3H/HeJ, (C57BL/6J × DBA/2J)F1, CD-1 Swiss, or N:NIH(S) mice generated NA cells, GM-CFUc, and CFUs for 20–41 weeks; cultures infected with Rauscher or other helper viruses generated them for 35–45 weeks. GM-CFUc and CFUs production in SFFV-positive cultures persisted for over 65 weeks and exceeded control levels by twentyfold to fiflyfold. The Rs of CFUs in SFFV-positive cultures was not detectably increased above control cultures. Multipotential (erythroid-neutrophil-mast cell-basophil-eosinophil) permanent FD cell clones were derived from control and SFFV-positive cultures. Thus SFFV amplifies the stem cell pool in vitro without detectably increasing the Rs capacity of CFUs.</description><subject>Animals</subject><subject>Blood Cell Count</subject><subject>Bone Marrow - microbiology</subject><subject>Cell Line</subject><subject>Friend murine leukemia virus - physiology</subject><subject>Hematopoietic Stem Cells - microbiology</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Virus Replication</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi0EKkvhyBHJJ27Z-iO2kyONGrZSEW2XFsQlcuIJckns4A_R9s7_JlJXXJnLHJ5Hr2ZehN5SsqWk5id3brAnimzZljP-DG1oKUnBKBHP0YYQpoqqUuVL9CrGO7JOzcojdCSFojWvN-jPpfcT3ttHwH7El1MOdvEJXLJ6wjuYdfKLt5DsgPcJZtzANEV87oYAOoLB1uHGr7bLPkd86h3gTzoE_xs3eUo5AO4fcBssOIP3ywTgcOuHHIvWh9m6H_jWhhxfoxejniK8OexjdNOefWl2xcXnj-fNh4vCMiVSUWs5SKmVYrrvDRjVU6r6si6FNrImldRDyUfDNa0oG6mpCdNiNHJQ3EBJR36M3j_lLsH_yhBTN9s4rC9pB-v9XUW4IpJU_xUpXxsUUqziu4OY-xlMtwQ76_DQHQpeefHEbUxw_w_r8LOTiivR7b59764afv31tFWd4H8B6OSOMQ</recordid><startdate>198302</startdate><enddate>198302</enddate><creator>Greenberger, Joel S.</creator><creator>Hottman, Nancy</creator><creator>Lieberman, Miriam</creator><creator>Botnick, LeslieE</creator><creator>Sakakeeny, Mary Ann</creator><creator>Eckner, Robert J.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>198302</creationdate><title>Pool Size of Pluripotential Hematopoietic Stem Cells Increased in Continuous Bone Marrow Culture by Friend Spleen Focus-Forming Virus</title><author>Greenberger, Joel S. ; Hottman, Nancy ; Lieberman, Miriam ; Botnick, LeslieE ; Sakakeeny, Mary Ann ; Eckner, Robert J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i275t-9a6c66a772abbded7b117b4945ad69086ac43fd3a1812f1d902a5fd6c73de41f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Animals</topic><topic>Blood Cell Count</topic><topic>Bone Marrow - microbiology</topic><topic>Cell Line</topic><topic>Friend murine leukemia virus - physiology</topic><topic>Hematopoietic Stem Cells - microbiology</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Greenberger, Joel S.</creatorcontrib><creatorcontrib>Hottman, Nancy</creatorcontrib><creatorcontrib>Lieberman, Miriam</creatorcontrib><creatorcontrib>Botnick, LeslieE</creatorcontrib><creatorcontrib>Sakakeeny, Mary Ann</creatorcontrib><creatorcontrib>Eckner, Robert J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Greenberger, Joel S.</au><au>Hottman, Nancy</au><au>Lieberman, Miriam</au><au>Botnick, LeslieE</au><au>Sakakeeny, Mary Ann</au><au>Eckner, Robert J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pool Size of Pluripotential Hematopoietic Stem Cells Increased in Continuous Bone Marrow Culture by Friend Spleen Focus-Forming Virus</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1983-02</date><risdate>1983</risdate><volume>70</volume><issue>2</issue><spage>323</spage><epage>331</epage><pages>323-331</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Continuous mouse bone marrow cultures were infected with Friend murine leukemia virus. Production of nonadherent (NA) and adherent cells, granulocyte-macrophage colony-forming unil(s) of progenitor cells (GM-CFUc), pluripotential hematopoietic stem cells (CFUs), the self-renewal potential (Rs) of CFUs, and generation of factor-dependent (FD) multipotenlial and committed permanent stem cell cloned lines were measured. Uninfected marrow cultures from C57BL/6J, C57BL/6JUt, B6.S, C3H/HeJ, (C57BL/6J × DBA/2J)F1, CD-1 Swiss, or N:NIH(S) mice generated NA cells, GM-CFUc, and CFUs for 20–41 weeks; cultures infected with Rauscher or other helper viruses generated them for 35–45 weeks. GM-CFUc and CFUs production in SFFV-positive cultures persisted for over 65 weeks and exceeded control levels by twentyfold to fiflyfold. The Rs of CFUs in SFFV-positive cultures was not detectably increased above control cultures. Multipotential (erythroid-neutrophil-mast cell-basophil-eosinophil) permanent FD cell clones were derived from control and SFFV-positive cultures. Thus SFFV amplifies the stem cell pool in vitro without detectably increasing the Rs capacity of CFUs.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>6571939</pmid><doi>10.1093/jnci/70.2.323</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Blood Cell Count Bone Marrow - microbiology Cell Line Friend murine leukemia virus - physiology Hematopoietic Stem Cells - microbiology Mice Mice, Inbred Strains Virus Replication |
title | Pool Size of Pluripotential Hematopoietic Stem Cells Increased in Continuous Bone Marrow Culture by Friend Spleen Focus-Forming Virus |
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