Loading…
Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential
We have previously identified a cellular population in murine bone marrow that facilitates engraftment of highly purified hematopoietic stem cells (HSC) across major histocompatibility complex (MHC) barriers without causing graft-versus-host disease. Here we investigated the effect of flt3 ligand (F...
Saved in:
Published in: | Blood 1998-11, Vol.92 (9), p.3177-3188 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93 |
---|---|
cites | cdi_FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93 |
container_end_page | 3188 |
container_issue | 9 |
container_start_page | 3177 |
container_title | Blood |
container_volume | 92 |
creator | Neipp, Michael Zorina, Tatiana Domenick, Michele A. Exner, Beate G. Ildstad, Suzanne T. |
description | We have previously identified a cellular population in murine bone marrow that facilitates engraftment of highly purified hematopoietic stem cells (HSC) across major histocompatibility complex (MHC) barriers without causing graft-versus-host disease. Here we investigated the effect of flt3 ligand (FL) and granulocyte colony-stimulating factor (G-CSF) on the mobilization of facilitating cells (FC) and HSC into peripheral blood (PB). Mice were injected with FL alone (day 1 to 10), G-CSF alone (day 4 to 10), or both in combination. The number of FC (CD8+/αβTCR−/γδTCR−) and HSC (lineage−/Sca-1+/c-kit+) was assessed daily by flow cytometry. Lethally irradiated allogeneic mice were reconstituted with PB mononuclear cells (PBMC). FL and G-CSF showed a highly significant synergy on the mobilization of FC and HSC. The peak efficiency for mobilization of FC (21-fold increase) and HSC (200-fold increase) was reached on day 10. Our data further suggest that the proliferation of FC and HSC induced by FL in addition to the mobilizing effect mediated by G-CSF might be responsible for the observed synergy of both growth factors. Finally, the engraftment potential of PBMC mobilized with FL and G-CSF or FL alone was superior to PBMC obtained from animals treated with G-CSF alone. Experiments comparing the engraftment potential of day 7 and day 10 mobilized PBMC indicate that day 10, during which both FC and HSC reached their maximum, might be the ideal time point for the collection of both populations. © 1998 by The American Society of Hematology. |
doi_str_mv | 10.1182/blood.V92.9.3177 |
format | article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1182_blood_V92_9_3177</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006497120578671</els_id><sourcerecordid>9787154</sourcerecordid><originalsourceid>FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93</originalsourceid><addsrcrecordid>eNp1kUtv1DAUhS0EKtPCng2SF2wz2HEedndoNNNWTAWiha3lONeVkWNHsadi-G_8N5xm6I6Fn-c714-D0DtK1pTy8mPnQujXP0S5FmtG2_YFWtG65AUhJXmJVoSQpqhES1-j8xh_EkIrVtZn6Ey0vKV1tUJ_tsaATjgYvNvfM7y3D8r3eG5Xk_IHF_QxAd4EF_yxuEt2ODiVrH_AO6VTmHDwePtrVD7aPJttt6Gzzv7OUN6Yyyqd12kxbcC5-IRdw6BSGIOFZDW-SzCcROvxrdVwiT9bP2sL_g3GMP47-mtI4JNV7g16ZZSL8PY0XqDvu-395rrYf7m62XzaF5qxJhVAhKa81V1PRC-qjhtoa97XTc0E5yx3oi0VJY0GpgzhVctV2ZDaQFebDgS7QGSpq6cQ4wRGjpMd1HSUlMg5CPkUhMxBSCHnILLl_WIZD90A_bPh9PNZ_3DSVdTKmfzZ2sZnrKwYEZxm7HLBID_v0cIko7bgNfR2yrnJPtj_3-Ev-5ipRg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential</title><source>ScienceDirect Journals</source><creator>Neipp, Michael ; Zorina, Tatiana ; Domenick, Michele A. ; Exner, Beate G. ; Ildstad, Suzanne T.</creator><creatorcontrib>Neipp, Michael ; Zorina, Tatiana ; Domenick, Michele A. ; Exner, Beate G. ; Ildstad, Suzanne T.</creatorcontrib><description>We have previously identified a cellular population in murine bone marrow that facilitates engraftment of highly purified hematopoietic stem cells (HSC) across major histocompatibility complex (MHC) barriers without causing graft-versus-host disease. Here we investigated the effect of flt3 ligand (FL) and granulocyte colony-stimulating factor (G-CSF) on the mobilization of facilitating cells (FC) and HSC into peripheral blood (PB). Mice were injected with FL alone (day 1 to 10), G-CSF alone (day 4 to 10), or both in combination. The number of FC (CD8+/αβTCR−/γδTCR−) and HSC (lineage−/Sca-1+/c-kit+) was assessed daily by flow cytometry. Lethally irradiated allogeneic mice were reconstituted with PB mononuclear cells (PBMC). FL and G-CSF showed a highly significant synergy on the mobilization of FC and HSC. The peak efficiency for mobilization of FC (21-fold increase) and HSC (200-fold increase) was reached on day 10. Our data further suggest that the proliferation of FC and HSC induced by FL in addition to the mobilizing effect mediated by G-CSF might be responsible for the observed synergy of both growth factors. Finally, the engraftment potential of PBMC mobilized with FL and G-CSF or FL alone was superior to PBMC obtained from animals treated with G-CSF alone. Experiments comparing the engraftment potential of day 7 and day 10 mobilized PBMC indicate that day 10, during which both FC and HSC reached their maximum, might be the ideal time point for the collection of both populations. © 1998 by The American Society of Hematology.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V92.9.3177</identifier><identifier>PMID: 9787154</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Bone Marrow Cells - drug effects ; Bone Marrow Cells - physiology ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Drug Synergism ; Graft Survival ; Granulocyte Colony-Stimulating Factor - pharmacology ; Hematopoietic Stem Cell Mobilization - methods ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells - drug effects ; Kinetics ; Male ; Medical sciences ; Membrane Proteins - pharmacology ; Mice ; Mice, Inbred C57BL ; Radiation Chimera ; Recombinant Proteins - pharmacology ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><ispartof>Blood, 1998-11, Vol.92 (9), p.3177-3188</ispartof><rights>1998 American Society of Hematology</rights><rights>1998 INIST-CNRS</rights><rights>Copyright 1998 by The American Society of Hematology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93</citedby><cites>FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006497120578671$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3547,27922,27923,45778</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2430981$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9787154$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neipp, Michael</creatorcontrib><creatorcontrib>Zorina, Tatiana</creatorcontrib><creatorcontrib>Domenick, Michele A.</creatorcontrib><creatorcontrib>Exner, Beate G.</creatorcontrib><creatorcontrib>Ildstad, Suzanne T.</creatorcontrib><title>Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential</title><title>Blood</title><addtitle>Blood</addtitle><description>We have previously identified a cellular population in murine bone marrow that facilitates engraftment of highly purified hematopoietic stem cells (HSC) across major histocompatibility complex (MHC) barriers without causing graft-versus-host disease. Here we investigated the effect of flt3 ligand (FL) and granulocyte colony-stimulating factor (G-CSF) on the mobilization of facilitating cells (FC) and HSC into peripheral blood (PB). Mice were injected with FL alone (day 1 to 10), G-CSF alone (day 4 to 10), or both in combination. The number of FC (CD8+/αβTCR−/γδTCR−) and HSC (lineage−/Sca-1+/c-kit+) was assessed daily by flow cytometry. Lethally irradiated allogeneic mice were reconstituted with PB mononuclear cells (PBMC). FL and G-CSF showed a highly significant synergy on the mobilization of FC and HSC. The peak efficiency for mobilization of FC (21-fold increase) and HSC (200-fold increase) was reached on day 10. Our data further suggest that the proliferation of FC and HSC induced by FL in addition to the mobilizing effect mediated by G-CSF might be responsible for the observed synergy of both growth factors. Finally, the engraftment potential of PBMC mobilized with FL and G-CSF or FL alone was superior to PBMC obtained from animals treated with G-CSF alone. Experiments comparing the engraftment potential of day 7 and day 10 mobilized PBMC indicate that day 10, during which both FC and HSC reached their maximum, might be the ideal time point for the collection of both populations. © 1998 by The American Society of Hematology.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells - drug effects</subject><subject>Bone Marrow Cells - physiology</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Drug Synergism</subject><subject>Graft Survival</subject><subject>Granulocyte Colony-Stimulating Factor - pharmacology</subject><subject>Hematopoietic Stem Cell Mobilization - methods</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Hematopoietic Stem Cells - drug effects</subject><subject>Kinetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Proteins - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Radiation Chimera</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNp1kUtv1DAUhS0EKtPCng2SF2wz2HEedndoNNNWTAWiha3lONeVkWNHsadi-G_8N5xm6I6Fn-c714-D0DtK1pTy8mPnQujXP0S5FmtG2_YFWtG65AUhJXmJVoSQpqhES1-j8xh_EkIrVtZn6Ey0vKV1tUJ_tsaATjgYvNvfM7y3D8r3eG5Xk_IHF_QxAd4EF_yxuEt2ODiVrH_AO6VTmHDwePtrVD7aPJttt6Gzzv7OUN6Yyyqd12kxbcC5-IRdw6BSGIOFZDW-SzCcROvxrdVwiT9bP2sL_g3GMP47-mtI4JNV7g16ZZSL8PY0XqDvu-395rrYf7m62XzaF5qxJhVAhKa81V1PRC-qjhtoa97XTc0E5yx3oi0VJY0GpgzhVctV2ZDaQFebDgS7QGSpq6cQ4wRGjpMd1HSUlMg5CPkUhMxBSCHnILLl_WIZD90A_bPh9PNZ_3DSVdTKmfzZ2sZnrKwYEZxm7HLBID_v0cIko7bgNfR2yrnJPtj_3-Ev-5ipRg</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>Neipp, Michael</creator><creator>Zorina, Tatiana</creator><creator>Domenick, Michele A.</creator><creator>Exner, Beate G.</creator><creator>Ildstad, Suzanne T.</creator><general>Elsevier Inc</general><general>The 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></search><sort><creationdate>19981101</creationdate><title>Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential</title><author>Neipp, Michael ; Zorina, Tatiana ; Domenick, Michele A. ; Exner, Beate G. ; Ildstad, Suzanne T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells - drug effects</topic><topic>Bone Marrow Cells - physiology</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Drug Synergism</topic><topic>Graft Survival</topic><topic>Granulocyte Colony-Stimulating Factor - pharmacology</topic><topic>Hematopoietic Stem Cell Mobilization - methods</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Hematopoietic Stem Cells - drug effects</topic><topic>Kinetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Proteins - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Radiation Chimera</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neipp, Michael</creatorcontrib><creatorcontrib>Zorina, Tatiana</creatorcontrib><creatorcontrib>Domenick, Michele A.</creatorcontrib><creatorcontrib>Exner, Beate G.</creatorcontrib><creatorcontrib>Ildstad, Suzanne T.</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><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neipp, Michael</au><au>Zorina, Tatiana</au><au>Domenick, Michele A.</au><au>Exner, Beate G.</au><au>Ildstad, Suzanne T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>1998-11-01</date><risdate>1998</risdate><volume>92</volume><issue>9</issue><spage>3177</spage><epage>3188</epage><pages>3177-3188</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>We have previously identified a cellular population in murine bone marrow that facilitates engraftment of highly purified hematopoietic stem cells (HSC) across major histocompatibility complex (MHC) barriers without causing graft-versus-host disease. Here we investigated the effect of flt3 ligand (FL) and granulocyte colony-stimulating factor (G-CSF) on the mobilization of facilitating cells (FC) and HSC into peripheral blood (PB). Mice were injected with FL alone (day 1 to 10), G-CSF alone (day 4 to 10), or both in combination. The number of FC (CD8+/αβTCR−/γδTCR−) and HSC (lineage−/Sca-1+/c-kit+) was assessed daily by flow cytometry. Lethally irradiated allogeneic mice were reconstituted with PB mononuclear cells (PBMC). FL and G-CSF showed a highly significant synergy on the mobilization of FC and HSC. The peak efficiency for mobilization of FC (21-fold increase) and HSC (200-fold increase) was reached on day 10. Our data further suggest that the proliferation of FC and HSC induced by FL in addition to the mobilizing effect mediated by G-CSF might be responsible for the observed synergy of both growth factors. Finally, the engraftment potential of PBMC mobilized with FL and G-CSF or FL alone was superior to PBMC obtained from animals treated with G-CSF alone. Experiments comparing the engraftment potential of day 7 and day 10 mobilized PBMC indicate that day 10, during which both FC and HSC reached their maximum, might be the ideal time point for the collection of both populations. © 1998 by The American Society of Hematology.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>9787154</pmid><doi>10.1182/blood.V92.9.3177</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-4971 |
ispartof | Blood, 1998-11, Vol.92 (9), p.3177-3188 |
issn | 0006-4971 1528-0020 |
language | eng |
recordid | cdi_crossref_primary_10_1182_blood_V92_9_3177 |
source | ScienceDirect Journals |
subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Bone Marrow Cells - drug effects Bone Marrow Cells - physiology Bone marrow, stem cells transplantation. Graft versus host reaction Drug Synergism Graft Survival Granulocyte Colony-Stimulating Factor - pharmacology Hematopoietic Stem Cell Mobilization - methods Hematopoietic Stem Cell Transplantation Hematopoietic Stem Cells - drug effects Kinetics Male Medical sciences Membrane Proteins - pharmacology Mice Mice, Inbred C57BL Radiation Chimera Recombinant Proteins - pharmacology Transfusions. Complications. Transfusion reactions. Cell and gene therapy |
title | Effect of FLT3 Ligand and Granulocyte Colony-Stimulating Factor on Expansion and Mobilization of Facilitating Cells and Hematopoietic Stem Cells in Mice: Kinetics and Repopulating Potential |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T02%3A38%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20FLT3%20Ligand%20and%20Granulocyte%20Colony-Stimulating%20Factor%20on%20Expansion%20and%20Mobilization%20of%20Facilitating%20Cells%20and%20Hematopoietic%20Stem%20Cells%20in%20Mice:%20Kinetics%20and%20Repopulating%20Potential&rft.jtitle=Blood&rft.au=Neipp,%20Michael&rft.date=1998-11-01&rft.volume=92&rft.issue=9&rft.spage=3177&rft.epage=3188&rft.pages=3177-3188&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood.V92.9.3177&rft_dat=%3Cpubmed_cross%3E9787154%3C/pubmed_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c336t-e09c187cbd09d94b8fe758d56539883398972a106ce3af08478a2605feb5fbe93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/9787154&rfr_iscdi=true |